Individual differences |
Methods | Statistics | Clinical | Educational | Industrial | Professional items | World psychology |
Biological: Behavioural genetics · Evolutionary psychology · Neuroanatomy · Neurochemistry · Neuroendocrinology · Neuroscience · Psychoneuroimmunology · Physiological Psychology · Psychopharmacology (Index, Outline)
Reelin is a protein that helps regulate processes of neuronal migration and positioning in the developing brain. Besides this important role in early development, reelin continues to work in the adult brain. It modulates the synaptic plasticity by enhancing the induction and maintenance of long-term potentiation. It also stimulates dendrite and dendritic spine development and regulates the continuing migration of neuroblasts generated in adult neurogenesis sites like subventricular and subgranular zones. It is found not only in the brain, but also in the spinal cord, blood, and other body organs and tissues.
Reelin has been suggested to be implicated in pathogenesis of several brain diseases. Significantly lowered expression of the protein have been found in schizophrenia and psychotic bipolar disorder, but the cause of it is uncertain as studies show that psychotropic medication itself affects RELN expression and the epigenetic hypothesis aimed at explaining the changed levels has received some contradictory evidence. Total lack of reelin causes a form of lissencephaly. Reelin also may play a role in Alzheimer's disease, temporal lobe epilepsy, and autism.
Reelin's name comes from the abnormal reeling gait of reeler mice, which were later found to have a deficiency of this brain protein and were homozygous for mutation of the RELN gene. The primary phenotype associated with loss of reelin function is a failure of neuronal positioning throughout the developing CNS. The mice heterozygous for the reelin gene, while having little neuroanatomical defects, display the endophenotypic traits linked to psychotic disorders.
Mutant mice provide insight into the underlying molecular mechanisms of the development of the CNS. Useful spontaneous mutations were first identified by scientists interested in motor behavior, and it proved relatively easy to screen littermates for mice that showed difficulties moving around the cage. A number of such mice were found and given descriptive names such as reeler, weaver, lurcher, nervous, and staggerer.
The "reeler" mouse was first described in the 1951 by D.S.Falconer in Edinburgh University as a spontaneous variant arising in a colony of mice maintained by geneticist Charlotte Auerbach.[How to reference and link to summary or text] Histopathological studies in the 1960s revealed that the cerebellum in reeler mice is dramatically decreased in size and the normal laminar organization found in several brain regions is disrupted. The 1970s brought the discovery of cellular layers inversion in the mice neocortex, which attracted more attention to the reeler mutation.
In 1994 a new allele of reeler was obtained by insertional mutagenesis (Miao et al., 1994). This provided the first molecular marker of the locus, permitting the gene, RELN gene to be mapped to chromosome 7q22 and subsequently cloned and identified (D'Arcangelo et al., 1995). Japanese scientists at Kochi Medical School successfully raised antibodies against normal brain extracts in reeler mice, later these antibodies were found to be specific monoclonal antibody for reelin, and were termed CR-50 (Cajal-Rezius marker 50). They noted that CR-50 reacted specifically with Cajal-Retzius neurons, whose functional role was unknown until then.
The Reelin receptors, apolipoprotein E receptor 2 (ApoER2) and very-low-density lipoprotein receptor (VLDLR), were discovered serendipitously by Trommsdorff et al, who found that the double knockout mice for ApoER2 and VLDLR, which they generated for another experiment, showed defects in cortical layering similar to that in reeler.
The downstream pathway of Reelin was further clarified using other mutant mice, including yotari and scrambler. These mutants have phenotypes similar to that of reeler but have no mutation in reelin. It was then demonstrated that the mouse disabled homologue 1 (Dab1) gene is responsible for the phenotypes of these mutant mice, as Dab1 protein was absent (yotari) or only barely (scrambler) detectable in these mutants. Targeted disruption of Dab1 also caused a phenotype similar to that of reeler. Pinpointing the DAB1 as a pivotal regulator of the reelin signaling cascade started the tedious process of deciphering its complex interactions.
There followed a series of speculative reports linking reelin's genetic variation and interactions to schizophrenia, Alzheimer's disease, autism and other highly complex dysfunctions. These and other discoveries, coupled with the perspective of unraveling the evolutionary changes that allowed for the creation of human brain, highly intensified the research. As of 2008, some 13 years after the gene coding the protein was discovered, hundreds of scientific articles address the multiple aspects of its structure and functioning. These aspects have been summarized by some of the researchers in a book called "Reelin Glycoprotein: Structure, Biology and Roles in Health and Disease" that saw print in 2008.
Tissue distribution and secretionEdit
Studies show that Reelin is absent from synaptic vesicles and is secreted via constitutive secretory pathway, being stored in Golgi secretory vesicles. Reelin's release rate is not regulated by depolarization, but strictly depends on its synthesis rate. This relationship is similar to that reported for the secretion of other ECM proteins.
During the brain development, reelin is secreted in the cortex and hippocampus by Cajal-Retzius cells, Cajal cells, and Retzius cells. Reelin-expressing cells in the prenatal and early postnatal brain are predominantly found in the marginal zone (MZ) of the cortex and in the temporary subpial granular layer (SGL), which is manifested to the highest extent in human, and in the hippocampal stratum lacunosum-moleculare and the upper marginal layer of the dentate gyrus.
Peaking just after the birth, the synthesis of reelin then goes down sharply and becomes more diffuse compared with the distinctly laminar expression in the developing brain. In the adult brain, Reelin is expressed by GABA-ergic interneurons of the cortex and glutamatergic cerebellar neurons, and by the few extant Cajal-Retzius cells. Among GABAergic interneurons, Reelin seems to be detected predominantly in those expressing calretinin and calbindin, like bitufted, horizontal, and Martinotti cells, but not parvalbumin-expressing cells, like chandelier or basket neurons. Outside the brain, reelin is found in adult mammalian blood, liver, pituitary pars intermedia, and adrenal chromaffin cells. In the liver, reelin is localized in hepatic stellate cells. The expression of Reelin increases when the liver is damaged, and returns to normal following its repair. 
The protein is also produced by the odontoblasts, cells at the margins of the dental pulp. Reelin is found here both during odontogenesis and in the mature tooth. Some authors suggest that odontoblasts play an additional role as sensory cells able to transduce pain signals to the nervous endings. According to the hypothesis, reelin participates in the proccess by enhancing the contact between odontoblasts and the nerve terminals.
Reelin is a secreted extracellular matrix glycoprotein composed of 3461 amino acids with a relative molecular mass of 388 kDa; its structural features allow for an enzymatic activity, making it a serine protease. Murine RELN gene consists of 65 exons spanning approximately 450 kb. One exon, coding for only two amino acids near the protein's C-terminal, undergoes alternative splicing, but the exact functional impact of this is unknown. Two transcription initiation sites and two polyadenilation sites are identified in the gene structure.
The Reelin protein starts with a signaling peptide 27 amino acids in length, followed by a region bearing similarity to F-spondin, marked as "SP" on the scheme, and by a region unique to reelin, marked as "H". Next comes 8 repeats of 300-350 amino acids. These are called reelin repeats and have an EGF motif at their center, dividing each repeat into two subrepeats, A and B. Despite this interruption, the two subdomains make direct contact, resulting in a compact overall structure.
The final Reelin domain contains a highly basic and short C-terminal region (CTR, marked "+") with a length of 32 amino acids. This region is highly conserved, being 100% identical in all investigated mammals. It was thought that CTR is necessary for reelin secretion, because Orleans reeler mutation, which lacks a part of 8th repeat and the whole CTR, is unable to secrete the misshaped protein, leading to its concentration in cytoplasm. However, one recent study has shown that the CTR is not essential for secretion, which is most probably hindered then reelin is cut along one of the repeats.
Reelin is cleaved in vivo at two sites located after domains 2 and 6 - approximately between repeats 2 and 3 and between repeats 6 and 7, resulting in the production of three fragments. This splitting does not decrease the protein's activity, as constructs made of the predicted central fragments (repeats 3–6) bind to lipoprotein receptors, trigger Dab1 phosphorylation and mimic functions of reelin during cortical plate development. Moreover, the processing of reelin by embryonic neurons may be necessary for proper corticogenesis.
The primary functions of Reelin are the regulation of corticogenesis and neuronal cell positioning in the prenatal period, but the protein is also implicated in a number of other processes, and the research is ongoing.
Reelin is found in numerous tissues and organs, and one could roughly subdivide its functional roles by the time of expression and by localisation of its action.
A number of non-nervous tissues and organs express reelin in the developing organism, with the expression sharply going down after the organ had been formed. The role of the protein here is largely unexplored, because the knockout mice show no major pathology in these organs. In the adult organism the non-neural expression is much less widespread, but goes up sharply when some organs are injured. The exact function of reelin upregulation following an injury is still being researched.
On the other hand, reelin's role in the growing CNS is more important and more explored. It promotes the differentiation of progenitor cells into radial glia and affects the orientation of its fibers, which serve as the guides for the migrating neuroblasts. The position of reelin-secreting cell layer is important, because the fibers orient themselves in the direction of its higher concentration.
Mammalian corticogenesis is another process where reelin plays a major role. In this process the temporary layer called preplate is split into the marginal zone on the top and subblate below, and the space between them is populated by neuronal layers in the inside-out pattern. Such an arrangement, where the newly created neurons pass through the settled layers and position themselves one step above, is a distinguishing feature of mammalian brain, in contrast to the evolutionary older reptile cortex, in which layers are positioned in an "outside-in" fashion. When reelin is absent, like in the mutant reeler mouse, the order of cortical layering becomes roughly inverted, with younger neurons finding themselves to be unable to pass the settled layers. Subplate neurons fail to stop and invade the upper most layer, creating the so-called superplate in which they mix with Cajal-Retzius cells and some cells normally destined for the second layer.
There is no agreement concerning the role of reelin in the proper positioning of cortical layers. The original hypothesis, that the protein is a stop signal for the migrating cells, is supported by its ability to induce the dissociation, its role in asserting the compact granule cell layer in the hippocampus, and by the fact that migrating neuroblasts evade the reelin-rich areas. But an experiment in which murine corticogenesis went normally despite the malpositioned reelin secreting layer, and lack of evidence that reelin affects the growth cones and leading edges of neurons, caused some additional hypotheses to be proposed. According to one of them, reelin makes the cells more susceptible to some yet undescribed positional signaling cascade.
The protein is thought to act on migrating neuronal precursors and thus controls correct cell positioning in the cortex and other brain structures. The proposed role is one of a dissociation signal for neuronal groups, allowing them to separate and go from tangential chain-migration to radial individual migration. Dissociation detaches migrating neurons from the glial cells that are acting as their guides, converting them into individual cells that can strike out alone to find their final position.
In the adult nervous system, reelin plays an eminent role at the two most active neurogenesis sites, the subventricular zone and the dentate gyrus. In some species, the neuroblasts from the subventricular zone migrate in chains in the rostral migratory stream (RMS) to reach the olfactory bulb, where reelin dissociates them into individual cells that are able to migrate further individually. They change their mode of migration from tangential to radial, and begin using the radial glia fibers as their guides. There are studies showing that along the RMS itself the two receptors, ApoER2 and VLDLR, and their intracellular adapter DAB1 function independently of Reelin, most likely by the influence of a newly proposed ligand, thrombospondin-1. In the adult dentate gyrus, reelin provides guidance cues for new neurons that are constantly arriving to the granule cell layer from subgranular zone, keeping the layer compact.
Reelin also plays an important role in the adult brain by modulating cortical pyramidal neuron dendritic spine expression density, the branching of dendrites, and the expression of long-term potentiation as its secretion is continued diffusely by the GABAegric cortical interneurons those origin is traced to the medial ganglionic eminence.
One study suggests that reelin may be the part of the mechanism behind the developmental change in the subunit composition of NMDA receptor, a major player in the memory and neuroplasticity processes. Reelin was shown to increase the mobility of its NR2B subunit.
Reelin-DAB1 interactions could have played a key role in the structural evolution of the cortex that evolved from a single layer in the common amniote predeccessor into multiple-layered cortex of contemporary mammals. Research shows that reelin expression goes up as the cortex becomes more complex, reaching the maximum in the human brain in which the reelin-secreting Cajal-Retzius cells have significantly more complex axonal arbour. Reelin is present in the telencephalon of all the vertebrates studied so far, but the pattern of expression is widely differential. For example, in zebra fish there are no Cajal-Retzius cells and the protein is being secreted by other neurons. These cells do not form a dedicated layer in amphibians, and radial migration in their brains is very weak.
As the cortex becomes more complex and convoluted, migration along the radial glia fibers becomes more important for the proper lamination. The emergence of a distinct reelin-secreting layer is thought to play an important role in this evolution. There are conflicting data concerning the importance of this layer, and these are explained in the literature either by the existence of an additional signaling positional mechanism that interacts with the reelin cascade, or by the assumption that mice that are used in such experiments have redundant secretion of reelin compared with more localized synthesis in the human brain.
Cajal-Retzius cells, most of which disappear around the time of birth, coexpress reelin with the HAR1 gene that is thought to have undergone the most significant evolutionary change in humans compared with chimpanzee, being the most «evolutionary accelerated» of the genes from the human accelerated regions discovered in 2006. There is evidence of an ongoing evolution in the reelin pathway: DAB1 gene variant was described in 2007 that has spread recently in the Chinese but not in another populations.
Mechanism of actionEdit
The main action of reelin is apparently conducted through the two members of Low density lipoprotein receptor gene family, VLDLR and the ApoER2. It also has been shown that alpha-3-beta-1 integrin receptor binds the N-terminal region of reelin, a site distinct from the region of reelin shown to associate with VLDLR/ApoER2. The proposal that the protocadherin CNR1 behaves as a Reelin receptor has been disproven.
Reelin receptors are present on both neurons and glial cells, with one study showing that the radial glia express the same amount of ApoER2 but being ten times less rich in VLDLR. One study suggests that beta-1 integrin receptors on glial cells play more important role in neuronal layering than the same receptors on the migrating neuroblasts.
The intracellular adaptor DAB1 binds to the VLDLR and ApoER2 through an NPxY motif and is involved in transmission of Reelin signals through these lipoprotein receptors. It becomes phosphorylated by Src and Fyn kinases and apparently stimulates the actin cytoskeleton to change its shape, affecting the proportion of integrin receptors on the cell surface, which leads to the change in adhesion. Phosphorylation of DAB1 leads to its ubiquitination and subsequent degradation, and this explains the hightened levels of DAB1 in the absence of reelin. Such negative feedback is thought to be important for proper cortical lamination. Activated by two antibodies, VLDLR and ApoER2 cause DAB1 phosphorylation but seemingly without the subsequent degradation and without rescuing the reeler phenotype, and this may indicate that a part of the signal is conducted independently of DAB1.
A protein having an important role in lissencephaly and accordingly called LIS1 (PAFAH1B1), was shown to interact with the intracellular segment of VLDLR, thus reacting to the activation of reelin pathway.
The two main reelin receptors seem to have slightly different roles: according to one study, VLDLR conducts the stop signal, while ApoER2 is essential for the migration of late-born neocortical neurons.
Reelin molecules have been shown to form a large protein complex, a disulfide-linked homodimer. If the homodimer fails to form, efficient tyrosine phosphorylation of DAB1 in vitro fails. Moreover, the two main receptors of reelin are able to form clusters that most probably play a major role in the signaling, causing the intracellular adaptor DAB1 to dimerize or oligomerize in its turn. Such clustering has been shown in the study to activate the signaling chain even in the absence of Reelin itself.
Reelin-dependent strengthening of long-term potentiation is caused by ApoER2 interaction with NMDA receptor. This interaction happens when ApoER2 has a region coded by exon 19. ApoER2 gene is alternatively spliced, with the exon 19-containing variant more actively produced during periods of activity. According to one study, the hippocampal reelin expression rapidly goes up when there is need to store a memory, as demethylases open up the RELN gene.
The activation of dendrite growth by reelin is apparently conducted through Src family kinases and is dependent upon the expression of Crk family proteins. Moreover, a Cre-loxP recombination mouse model that lacks Crk and CrkL in most neurons was reported to have the reeler phenotype, indicating that Crk/CrkL lie between DAB1 and Akt in the reelin signaling chain.
One study shows that proper corticogenesis in vivo is highly dependent upon reelin being processed by embrionic neurons, which are thought to secrete some as yet unidentified metalloproteinases that free the central signal-competent part of the protein. Some other unknown proteolytic mechanisms may also play a role. It is supposed that full-sized reelin stucks to the extracellular matrix fibers on the higher levels, and the central fragments, as they are being freed up by the breaking up of reelin, are able to permeate into the lower levels. It is possible that as neuroblasts reach the higher levels they stop their migration either because of the heightened combined expression of all forms of reelin, or due to the peculiar mode of action of the full-sized reelin molecules and its homodimers.
Interaction with Cdk5 Edit
Cyclin-dependent kinase 5 (Cdk5), a major regulator of neuronal migration and positioning, is known to phosphorylate DAB1 and other cytosolic targets of reelin signaling, such as Tau, which could be activated also via reelin-induced deactivation of GSK3B, and NUDEL, associated with Lis1, one of the DAB1 targets. LTP induction by reelin in hippocampal slices fails in p35 knockouts. P35 is a key Cdk5 activator, and double p35/Dab1, p35/RELN, p35/ApoER2, p35/VLDLR knockouts display increased neuronal migration deficits, indicating a synergistic action of reelin->ApoER2/VLDLR->DAB1 and p35/p39->Cdk5 pathways in the normal corticogenesis.
Possible pathological role Edit
Disruptions of the RELN gene are considered to be the cause of the rare form of lissencephaly with cerebellar hypoplasia called Norman-Roberts syndrome. The mutations disrupt splicing of RELN cDNA, resulting in low or undetectable amounts of reelin protein. The phenotype in these patients was characterized by hypotonia, ataxia, and developmental delay, with lack of unsupported sitting and profound mental retardation with little or no language development. Seizures and congenital lymphedema were also present. A novel chromosomal translocation causing the syndrome was described in 2007. The mutations affecting reelin in human are usually associated with consanguineous marriage.
Reduced expression of reelin and its mRNA levels in the brains of schizophrenia sufferers had been reported in 1998 and 2000 and independently confirmed in the postmortem studies of hippocampus, cerebellum, basal ganglia, and in the cortex studies. The reduction may reach up to 50% in some brain regions and is coupled with reduced expression of GAD-67 enzyme, which catalyses the transition of glutamate to GABA. Blood levels of reelin and its isoforms are also altered in schizophrenia, along with mood disorders, according to one study. Reduced reelin mRNA prefrontal expression in schizophrenia was found to be the most statistically relevant disturbance found in the multicenter study conducted in 14 separate laboratories in 2001 by Stanley Foundation Neuropathology Consortium.
Epigenetic hypermethylation of DNA in schizophrenia patients is proposed as a cause of the reduction, in agreement with the observations dating from the 1960s that administration of methionine to schizophrenic patients results in a profound exacerbation of schizophrenia symptoms in sixty to seventy percent of patients. The proposed mechanism is a part of the "epigenetic hypothesis for schizophrenia pathophysiology" formulated in 2008. A postmortem study comparing DNMT1 and Reelin mRNA expression in cortical layers I and V of schizophrenic patients and normal controls demonstrated that in the layer V both DNMT1 and Reelin levels were normal, while in the layer I DNMT1 was threefold higher, probably leading to the twofold decrease in the Reelin expression. There is evidence that the change is selective, and DNMT1 is overexpressed in reelin-secreting GABAegric neurons but not in their glutamatergic neighbours. Methylation inhibitors and histone deacetylase inhibitors, such as valproic acid, increase reelin mRNA levels, while L-methionine treatment downregulates the phenotypic expression of reelin. One study indicated the upregulation of histone deacetylase HDAC1 in the hippocampi of patients. Histone deacetylases supress gene promoters; hyperacetylation of hystones was shown in murine models to demethylate the promoters of both reelin and GAD67. DNMT1 inhibitors in animals have been shown to increase the expression of both reelin and GAD67, and both DNMT inhibitors and HDAC inhibitors shown in one study to activate both genes with comparable dose- and time-dependence. As one study shows, SAM concentration in patients' prefrontal cortex is twice as high as in the cortices of non-affected people. SAM, being a methyl group donor necessary for DNMT activity, could further shift epigenetic control of gene expression.
The factors mentioned above serve to corroborate the epigenetic hypothesis. But it is worth mentioning that in contrast with initial data, two recent studies have failed to confirm the RELN hypermethylation, and psychotropic medication could in itself affect the reelin expression in the brain, as animal studies show (see below).
Other interesting findings probably linking reelin pathway to developmental hypotheses of schizophrenia are noted in the studies on mice that are either prenatally infected with influenza virus or have their immune system activated artificially during pregnancy. The Cajal-Retzius cells in the newborns secrete significantly less reelin despite keeping their expression of calretinin and nNos within normal range. These data run in parallel with the findings of increased risk of schizophrenia in humans after a prenatal infection during the second trimester.
Chromosome region 7q22 that harbours the RELN gene is associated with schizophrenia, and the gene itself was associated with the disease in a large study that found the polymorphism rs7341475 to increase the risk of the disease in women, but not in men. The women that have the SNP are about 1.4 times more likely to get ill, according to the study. Allelic variations of RELN have also been correlated with working memory, memory and executive functioning in nuclear families where one of the members suffers from schizophrenia. In one small study, nonsynonymous polymorphism Val997Leu of the gene was associated with left and right vetricular enlargement in patients.
One study showed that patients have decreased levels of one of reelin receptors, VLDLR, in the peripheral lymphocytes. After six months of antipsychotic therapy the expression went up; according to authors, peripheral VLRLR levels may serve as a reliable peripheral biomarker of schizophrenia.
Considering the role of reelin in promoting dendritogenesis, suggestions were made that the localized dendritic spine deficit observed in schizophrenia  could be in part connected with the downregulation of reelin.
Reelin pathway could also be linked to schizophrenia and other psychotic disorders through its interaction with risk genes. One example is the neuronal transcription factor NPAS3, disruption of which is linked to schizophrenia and learning disability. Knockout mice lacking NPAS3 or the similar protein NPAS1 have significantly lower levels of reelin; the precise mechanism behind this is unknown. Another example is the schizophrenia-linked gene MTHFR, with murine knockouts showing decreased levels of reelin in the cerebellum. Along the same line, it is worth noting that the gene coding for the subunit NR2B that is presumably affected by reelin in the process of NR2B->NR2A developmental change of NMDA receptor composition, stands as one of the strongest risk gene candidates.
The heterozygous reeler mouse, which is haploinsufficient for the RELN gene, shares several neurochemical and behavioral abnormalities with schizophrenia and bipolar disorder, but is considered not suitable for use as a genetic mouse model of schizophrenia.
Bipolar disorder Edit
Decrease in RELN expression with concurrent upregulation of DNMT1 is typical of bipolar disorder with psychosis, but is not characteristic of patients with major depression without psychosis, which could speak of specific association of the change with psychoses. One study suggests that unlike in schizophrenia, such changes are found only in the cortex and do not affect the deeper structures in psychotic bipolar patients, as their basal ganglia were found to have the normal levels of DNMT1 and subsequently both the reelin and GAD67 levels were within the normal range.
The role of reelin in autism is not decided yet: three studies provide no link, two other works suggest that the genetic variations of RELN may have an effect. In one study, a postmortem analysis of five patients showed decrease of reelin expression in the cerebellar cortex. A study conducted in 2002 detected decreased blood levels of reelin in both patients and their relatives.
Temporal lobe epilepsy: granule cell dispersionEdit
Decreased reelin expression in the hippocampal tissue samples from patients with temporal lobe epilepsy was found to be directly correlated with the extent of granule cell dispersion (GCD), a major feature of the disease that is noted in 45%-73% of patients. According to one study, prolonged seizures in a rat model of mesial temporal lobe epilepsy have led to the loss of reelin-expressing interneurons and subsequent ectopic chain migration and aberrant integration of newborn dentate granule cells. Without reelin, the chain-migrating neuroblasts failed to detach properly. Moreover, in a kainate-induced mouse epilepsy model, exogenous reelin had prevented GCD, according to one study.
According to one study, reelin expression and glycosylation patterns are altered in Alzheimer's disease. In the cortex of the patients, reelin levels were 40% higher compared with controls, but the cerebellar levels of the protein remain normal in the same patients. This finding is in agreement with an earlier study showing the presence of Reelin associated with amyloid plaques in a transgenic AD mouse model. A large genetic study of 2008 showed that RELN gene variation is associated with an increased risk of Alzheimer's disease in women. The number of reelin-producing Cajal-Retzius cells is significantly decreased in first cortical layer of patients. Some authors consider the reelin pathway to be a link between the Alzheimer's disease and schizophrenia.
DNA methylation patterns are often changed in tumours, and RELN gene could be affected: according to one study, in the pancreatic cancer the expression is suppressed, along with other reelin pathway components In the same study, cutting the reelin pathway in cancer cells that still expressed reelin resulted in increased motility and invasiveness. On the contrary, in prostate cancer the RELN expression is excessive and correlates with Gleason score. Retinoblastoma presents another example of RELN overexpression.
Other conditions Edit
Psychotropic medication and reelin expression Edit
As reelin is being implicated in a number of brain disorders and its expression is usually measured posthumously, assessing the possible medication effects is important.
According to the epigenetic hypothesis, drugs that shift the balance in favour of demethylation have a potential to alleviate the proposed methylation-caused downregulation of RELN and GAD67. In one study, clozapine and sulpiride but not haloperidol and olanzapine were shown to increase the demethylation of both genes in mice pretreated with l-methionine. Valproic acid, a histone deacetylase inhibitor, when taken in combination with antipsychotics, is proposed to have some benefits. But there are studies conflicting the main premise of the epigenetic hypothesis, and a study by Fatemi et al shows no increase in RELN expression by valproic acid; that indicates the need for further investigation.
|Reelin expression||Clozapine||Fluoxetine||Haloperidol||Lithium||Olanzapine||Valproic Acid|
- ↑ Weeber EJ, Beffert U, Jones C, et al (October 2002). Reelin and ApoE receptors cooperate to enhance hippocampal synaptic plasticity and learning. J. Biol. Chem. 277 (42): 39944–52.W
- ↑ 2.0 2.1 D'Arcangelo G (August 2005). Apoer2: a reelin receptor to remember. Neuron 47 (4): 471–3.
- ↑ 3.0 3.1 Niu S, Renfro A, Quattrocchi CC, Sheldon M, D'Arcangelo G (January 2004). Reelin promotes hippocampal dendrite development through the VLDLR/ApoER2-Dab1 pathway. Neuron 41 (1): 71–84.
- ↑ Niu S, Yabut O, D'Arcangelo G (October 2008). The Reelin signaling pathway promotes dendritic spine development in hippocampal neurons. The Journal of neuroscience : the official journal of the Society for Neuroscience 28 (41): 10339–48.
- ↑ 5.0 5.1 Grayson DR, Guidotti A, Costa E. Current Hypotheses. Schizophrenia Research Forum. schizophreniaforum.org. URL accessed on 2008-08-23.
- ↑ 6.0 6.1 Tochigi M, Iwamoto K, Bundo M, Komori A, Sasaki T, Kato N, Kato T (2007). Methylation Status of the Reelin Promoter Region in the Brain of Schizophrenic Patients. Biological Psychiatry 63: 530.
- ↑ 7.0 7.1 Mill J, Tang T, Kaminsky Z, Khare T, Yazdanpanah S, Bouchard L, Jia P, Assadzadeh A, Flanagan J, Schumacher A, Wang SC, Petronis A (2008). Epigenomic profiling reveals DNA-methylation changes associated with major psychosis. Am. J. Hum. Genet. 82 (3): 696–711.
- ↑ 8.0 8.1 Falconer DS (January 1951), "Two new mutants, ‘trembler’ and ‘reeler’, with neurological actions in the house mouse (Mus musculus L.)", Journal of Genetics 50 (2): 192–201, doi:10.1007/BF02996215, http://www.ias.ac.in/jarch/jgenet/50/192.pdf
- ↑ Tueting P, Doueiri MS, Guidotti A, Davis JM, Costa E (2006). Reelin down-regulation in mice and psychosis endophenotypes. Neurosci Biobehav Rev 30 (8): 1065–77.
- ↑ Hamburgh M (October 1963). Analysis of the postnatal developmental effects of "reeler", a neurological mutation in mice. A study in developmental genetics. Dev. Biol. 19: 165–85.
- ↑ Caviness VS (December 1976). Patterns of cell and fiber distribution in the neocortex of the reeler mutant mouse. J. Comp. Neurol. 170 (4): 435–47.
- ↑ Miao GG, Smeyne RJ, D'Arcangelo G, Copeland NG, Jenkins NA, Morgan JI, Curran T (November 1994). Isolation of an allele of reeler by insertional mutagenesis. Proc. Natl. Acad. Sci. U.S.A. 91 (23): 11050–4.
- ↑ D'Arcangelo G, Miao GG, Chen SC, Soares HD, Morgan JI, Curran T (April 1995). A protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature 374 (6524): 719–23.
- ↑ Ogawa M, Miyata T, Nakajima K, et al (May 1995). The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons. Neuron 14 (5): 899–912.
- ↑ Trommsdorff M, Gotthardt M, Hiesberger T, et al (June 1999). Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2. Cell 97 (6): 689–701.
- ↑ Sheldon M, Rice DS, D'Arcangelo G, et al (October 1997). Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice. Nature 389 (6652): 730–3.
- ↑ "Reelin" mentioned in the titles of scientific literature - a search in the Google Scholar
- ↑ 18.0 18.1 18.2 18.3 18.4 (2008) Hossein S. Fatemi Reelin Glycoprotein: Structure, Biology and Roles in Health and Disease, 444, Springer.
- ↑ Lacor PN, Grayson DR, Auta J, Sugaya I, Costa E, Guidotti A (March 2000). Reelin secretion from glutamatergic neurons in culture is independent from neurotransmitter regulation. Proc. Natl. Acad. Sci. U.S.A. 97 (7): 3556–61.
- ↑ Meyer G, Goffinet AM, Fairén A (December 1999). What is a Cajal-Retzius cell? A reassessment of a classical cell type based on recent observations in the developing neocortex. Cereb. Cortex 9 (8): 765–75.
- ↑ 21.0 21.1 Meyer G, Goffinet AM (July 1998). Prenatal development of reelin-immunoreactive neurons in the human neocortex. J. Comp. Neurol. 397 (1): 29–40.
- ↑ Schiffmann SN, Bernier B, Goffinet AM (May 1997). Reelin mRNA expression during mouse brain development. Eur. J. Neurosci. 9 (5): 1055–71.
- ↑ Pesold C, Impagnatiello F, Pisu MG, et al (March 1998). Reelin is preferentially expressed in neurons synthesizing gamma-aminobutyric acid in cortex and hippocampus of adult rats. Proc. Natl. Acad. Sci. U.S.A. 95 (6): 3221–6.
- ↑ Alcántara S, Ruiz M, D'Arcangelo G, et al (October 1998). Regional and cellular patterns of reelin mRNA expression in the forebrain of the developing and adult mouse. J. Neurosci. 18 (19): 7779–99.
- ↑ Pesold C, Liu WS, Guidotti A, Costa E, Caruncho HJ (March 1999). Cortical bitufted, horizontal, and Martinotti cells preferentially express and secrete reelin into perineuronal nets, nonsynaptically modulating gene expression. Proc. Natl. Acad. Sci. U.S.A. 96 (6): 3217–22.
- ↑ Smalheiser NR, Costa E, Guidotti A, et al (February 2000). Expression of reelin in adult mammalian blood, liver, pituitary pars intermedia, and adrenal chromaffin cells. Proc. Natl. Acad. Sci. U.S.A. 97 (3): 1281–6.
- ↑ Samama B, Boehm N (July 2005). Reelin immunoreactivity in lymphatics and liver during development and adult life. Anat Rec a Discov Mol Cell Evol Biol 285 (1): 595–9.
- ↑ 28.0 28.1 Kobold D, Grundmann A, Piscaglia F, et al (May 2002). Expression of reelin in hepatic stellate cells and during hepatic tissue repair: a novel marker for the differentiation of HSC from other liver myofibroblasts. J. Hepatol. 36 (5): 607–13.
- ↑ 29.0 29.1 Pulido JS, Sugaya I, Comstock J, Sugaya K (June 2007). Reelin expression is upregulated following ocular tissue injury. Graefes Arch. Clin. Exp. Ophthalmol. 245 (6): 889–93.
- ↑ Buchaille R, Couble ML, Magloire H, Bleicher F (September 2000). A substractive PCR-based cDNA library from human odontoblast cells: identification of novel genes expressed in tooth forming cells. Matrix biology : journal of the International Society for Matrix Biology 19 (5): 421–30.
- ↑ Allard B, Magloire H, Couble ML, Maurin JC, Bleicher F (September 2006). Voltage-gated sodium channels confer excitability to human odontoblasts: possible role in tooth pain transmission. The Journal of biological chemistry 281 (39): 29002–10.
- ↑ Maurin JC, Couble ML, Didier-Bazes M, Brisson C, Magloire H, Bleicher F (August 2004). Expression and localization of reelin in human odontoblasts. Matrix biology : journal of the International Society for Matrix Biology 23 (5): 277–85.
- ↑ Yasui N, Nogi T, Kitao T, Nakano Y, Hattori M, Takagi J (June 2007). Structure of a receptor-binding fragment of reelin and mutational analysis reveal a recognition mechanism similar to endocytic receptors. Proc. Natl. Acad. Sci. U.S.A. 104 (24): 9988–93.
- ↑ 34.0 34.1 Quattrocchi CC, Wannenes F, Persico AM, Ciafré SA, D'Arcangelo G, Farace MG, Keller F. (January 2002). Reelin is a serine protease of the extracellular matrix. J. Biol. Chem. 277 (1): 303–9.
- ↑ 35.0 35.1 Royaux I, Lambert de Rouvroit C, D'Arcangelo G, Demirov D, Goffinet AM (December 1997). Genomic organization of the mouse reelin gene. Genomics 46 (2): 240–50.
- ↑ Nogi T, Yasui N, Hattori M, Iwasaki K, Takagi J (August 2006). Structure of a signaling-competent reelin fragment revealed by X-ray crystallography and electron tomography. Embo J. 25 (15): 3675–83.
- ↑ Nakano Y, Kohno T, Hibi T, et al (July 2007). The extremely conserved C-terminal region of Reelin is not necessary for secretion but is required for efficient activation of downstream signaling. J. Biol. Chem. 282 (28): 20544–52.
- ↑ Lambert de Rouvroit C, de Bergeyck V, Cortvrindt C, Bar I, Eeckhout Y, Goffinet AM (March 1999). Reelin, the extracellular matrix protein deficient in reeler mutant mice, is processed by a metalloproteinase. Exp. Neurol. 156 (1): 214–7.
- ↑ 39.0 39.1 39.2 Jossin Y, Ignatova N, Hiesberger T, Herz J, Lambert de Rouvroit C, Goffinet AM (January 2004). The central fragment of Reelin, generated by proteolytic processing in vivo, is critical to its function during cortical plate development. J. Neurosci. 24 (2): 514–21.
- ↑ 40.0 40.1 40.2 Jossin Y, Gui L, Goffinet AM (April 2007). Processing of Reelin by embryonic neurons is important for function in tissue but not in dissociated cultured neurons. J. Neurosci. 27 (16): 4243–52.
- ↑ 41.0 41.1 Blake SM, Strasser V, Andrade N, et al (October 2008). Thrombospondin-1 binds to ApoER2 and VLDL receptor and functions in postnatal neuronal migration. The EMBO journal.
- ↑ Lennington JB, Yang Z, Conover JC (November 2003). Neural stem cells and the regulation of adult neurogenesis. Reprod. Biol. Endocrinol. 1: 99.
- ↑ 43.0 43.1 43.2 43.3 43.4 Nomura T, Takahashi M, Hara Y, Osumi N (2008). Patterns of neurogenesis and amplitude of Reelin expression are essential for making a mammalian-type cortex. PLoS ONE 3 (1): e1454.
- ↑ 44.0 44.1 Hartfuss E, Förster E, Bock HH, et al (October 2003). Reelin signaling directly affects radial glia morphology and biochemical maturation. Development 130 (19): 4597–609.
- ↑ 45.0 45.1 Hack I, Bancila M, Loulier K, Carroll P, Cremer H (October 2002). Reelin is a detachment signal in tangential chain-migration during postnatal neurogenesis. Nat. Neurosci. 5 (10): 939–45.
- ↑ 46.0 46.1 46.2 Yoshida M, Assimacopoulos S, Jones KR, Grove EA (February 2006). Massive loss of Cajal-Retzius cells does not disrupt neocortical layer order. Development 133 (3): 537–45.
- ↑ Andrade N, Komnenovic V, Blake SM, et al (May 2007). ApoER2/VLDL receptor and Dab1 in the rostral migratory stream function in postnatal neuronal migration independently of Reelin. Proceedings of the National Academy of Sciences of the United States of America 104 (20): 8508–13.
- ↑ Frotscher M, Haas CA, Förster E (June 2003). Reelin controls granule cell migration in the dentate gyrus by acting on the radial glial scaffold. Cereb. Cortex 13 (6): 634–40.
- ↑ 49.0 49.1 Groc L, Choquet D, Stephenson FA, Verrier D, Manzoni OJ, Chavis P (2007). NMDA receptor surface trafficking and synaptic subunit composition are developmentally regulated by the extracellular matrix protein Reelin. J. Neurosci. 27 (38): 10165–75.
- ↑ Bar I, Lambert de Rouvroit C, Goffinet AM (December 2000). The evolution of cortical development. An hypothesis based on the role of the Reelin signaling pathway. Trends Neurosci. 23 (12): 633–8.
- ↑ Molnár Z, Métin C, Stoykova A, et al (February 2006). Comparative aspects of cerebral cortical development. Eur. J. Neurosci. 23 (4): 921–34.
- ↑ 52.0 52.1 Pérez-García CG, González-Delgado FJ, Suárez-Solá ML, et al (January 2001). Reelin-immunoreactive neurons in the adult vertebrate pallium. J. Chem. Neuroanat. 21 (1): 41–51.
- ↑ Costagli A, Kapsimali M, Wilson SW, Mione M (August 2002). Conserved and divergent patterns of Reelin expression in the zebrafish central nervous system. J. Comp. Neurol. 450 (1): 73–93.
- ↑ Goffinet AM (2006). What makes us human? A biased view from the perspective of comparative embryology and mouse genetics. J Biomed Discov Collab 1: 16.
- ↑ Pollard KS, Salama SR, Lambert N, et al (September 2006). An RNA gene expressed during cortical development evolved rapidly in humans. Nature 443 (7108): 167–72.
- ↑ Williamson SH, Hubisz MJ, Clark AG, Payseur BA, Bustamante CD, Nielsen R (2007). Localizing Recent Adaptive Evolution in the Human Genome. PLoS Genetics 3 (6): e90.
- ↑ Wade N. Humans Have Spread Globally, and Evolved Locally. Science. New York Times. URL accessed on 2008-08-23.
- ↑ 58.0 58.1 Zhang G, Assadi AH, McNeil RS, Beffert U, Wynshaw-Boris A, Herz J, Clark GD, D’Arcangelo G. (2007). The Pafah1b complex interacts with the Reelin receptor VLDLR. PLoS ONE 2 (2): e252.
- ↑ Schmid RS, Jo R, Shelton S, Kreidberg JA, Anton ES (October 2005). Reelin, integrin and DAB1 interactions during embryonic cerebral cortical development. Cereb. Cortex 15 (10): 1632–6.
- ↑ Senzaki K, Ogawa M, Yagi T (December 1999). Proteins of the CNR family are multiple receptors for Reelin. Cell 99 (6): 635–47.
- ↑ Belvindrah R, Graus-Porta D, Goebbels S, Nave KA, Müller U (December 2007). Beta1 integrins in radial glia but not in migrating neurons are essential for the formation of cell layers in the cerebral cortex. J. Neurosci. 27 (50): 13854–65.
- ↑ Howell BW, Gertler FB, Cooper JA (January 1997). Mouse disabled (mDab1): a Src binding protein implicated in neuronal development. EMBO J. 16 (1): 121–32.
- ↑ Arnaud L, Ballif BA, Förster E, Cooper JA (January 2003). Fyn tyrosine kinase is a critical regulator of disabled-1 during brain development. Curr. Biol. 13 (1): 9–17.
- ↑ Feng L, Allen NS, Simo S, Cooper JA (November 2007). Cullin 5 regulates Dab1 protein levels and neuron positioning during cortical development. Genes Dev. 21 (21): 2717–30.
- ↑ Kerjan G, Gleeson JG (November 2007). A missed exit: Reelin sets in motion Dab1 polyubiquitination to put the break on neuronal migration. Genes Dev. 21 (22): 2850–4.
- ↑ 66.0 66.1 Keilani S, Sugaya K (July 2008). Reelin induces a radial glial phenotype in human neural progenitor cells by activation of Notch-1. BMC Dev. Biol. 8 (1): 69.
- ↑ Hack I, Hellwig S, Junghans D, Brunne B, Bock HH, Zhao S, Frotscher M (2007). Divergent roles of ApoER2 and Vldlr in the migration of cortical neurons. Development 134 (21): 3883–91.
- ↑ Utsunomiya-Tate N, Kubo K, Tate S, et al (August 2000). Reelin molecules assemble together to form a large protein complex, which is inhibited by the function-blocking CR-50 antibody. Proc. Natl. Acad. Sci. U.S.A. 97 (17): 9729–34.
- ↑ Kubo K, Mikoshiba K, Nakajima K (August 2002). Secreted Reelin molecules form homodimers. Neurosci. Res. 43 (4): 381–8.
- ↑ 70.0 70.1 Strasser V, Fasching D, Hauser C, et al (February 2004). Receptor clustering is involved in Reelin signaling. Molecular and cellular biology 24 (3): 1378–86.
- ↑ Beffert U, Weeber EJ, Durudas A, et al (August 2005). Modulation of synaptic plasticity and memory by Reelin involves differential splicing of the lipoprotein receptor Apoer2. Neuron 47 (4): 567–79.
- ↑ Miller CA, Sweatt JD (March 2007). Covalent modification of DNA regulates memory formation. Neuron 53 (6): 857–69.
- ↑ 73.0 73.1 Matsuki T, Pramatarova A, Howell BW (May 2008). Reduction of Crk and CrkL expression blocks reelin-induced dendritogenesis. J. Cell. Sci. 121: 1869.
- ↑ Park TJ, Curran T (December 2008). Crk and crk-like play essential overlapping roles downstream of disabled-1 in the reelin pathway. J. Neurosci. 28 (50): 13551–62.
- ↑ Lugli G, Krueger JM, Davis JM, Persico AM, Keller F, Smalheiser NR (September 2003). Methodological factors influencing measurement and processing of plasma reelin in humans. BMC Biochem. 4: 9.
- ↑ Arnaud L, Ballif BA, Cooper JA (December 2003). Regulation of protein tyrosine kinase signaling by substrate degradation during brain development. Mol. Cell. Biol. 23 (24): 9293-302.
- ↑ Ohshima T, Suzuki H, Morimura T, Ogawa M, Mikoshiba K (April 2007). Modulation of Reelin signaling by Cyclin-dependent kinase 5. Brain Res. 1140: 84-95.
- ↑ Keshvara L, Magdaleno S, Benhayon D, Curran T (June 2002). Cyclin-dependent kinase 5 phosphorylates disabled 1 independently of Reelin signaling. J. Neurosci. 22 (12): 4869-77.
- ↑ Kobayashi S, Ishiguro K, Omori A, Takamatsu M, Arioka M, Imahori K, Uchida T (December 1993). A cdc2-related kinase PSSALRE/cdk5 is homologous with the 30 kDa subunit of tau protein kinase II, a proline-directed protein kinase associated with microtubule. FEBS Lett. 335 (2): 171-5.
- ↑ Beffert U, Morfini G, Bock HH, Reyna H, Brady ST, Herz J (December 2002). Reelin-mediated signaling locally regulates protein kinase B/Akt and glycogen synthase kinase 3beta. J. Biol. Chem. 277 (51): 49958-64.
- ↑ Sasaki S, Shionoya A, Ishida M, Gambello MJ, Yingling J, Wynshaw-Boris A, Hirotsune S (December 2000). A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system. Neuron 28 (3): 681-96.
- ↑ 82.0 82.1 Beffert U, Weeber EJ, Morfini G, Ko J, Brady ST, Tsai LH, Sweatt JD, Herz J (February 2004). Reelin and cyclin-dependent kinase 5-dependent signals cooperate in regulating neuronal migration and synaptic transmission. J. Neurosci. 24 (8): 1897-906.
- ↑ Ohshima T, Ogawa M, Veeranna, Hirasawa M, Longenecker G, Ishiguro K, Pant HC, Brady RO, Kulkarni AB, Mikoshiba K (February 2001). Synergistic contributions of cyclin-dependant kinase 5/p35 and Reelin/Dab1 to the positioning of cortical neurons in the developing mouse brain. Proc. Natl. Acad. Sci. U.S.A. 98 (5): 2764-9.
- ↑ Hong SE, Shugart YY, Huang DT, et al (September 2000). Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. Nat. Genet. 26 (1): 93–6.
- ↑ Crino P (November 2001). New RELN Mutation Associated with Lissencephaly and Epilepsy. Epilepsy Curr 1 (2): 72.
- ↑ Zaki M, Shehab M, El-Aleem AA, et al (May 2007). Identification of a novel recessive RELN mutation using a homozygous balanced reciprocal translocation. Am. J. Med. Genet. A 143A (9): 939–44.
- ↑ Impagnatiello F, Guidotti AR, Pesold C, et al (December 1998). A decrease of reelin expression as a putative vulnerability factor in schizophrenia. Proc. Natl. Acad. Sci. U.S.A. 95 (26): 15718–23.
- ↑ 88.0 88.1 Guidotti A, Auta J, Davis JM, et al (November 2000). Decrease in reelin and glutamic acid decarboxylase67 (GAD67) expression in schizophrenia and bipolar disorder: a postmortem brain study. Arch. Gen. Psychiatry 57 (11): 1061–9.
- ↑ Fatemi SH, Earle JA, McMenomy T (November 2000). Reduction in Reelin immunoreactivity in hippocampus of subjects with schizophrenia, bipolar disorder and major depression. Mol. Psychiatry 5 (6): 654–63, 571.
- ↑ 90.0 90.1 Fatemi SH, Hossein Fatemi S, Stary JM, Earle JA, Araghi-Niknam M, Eagan E (January 2005). GABAergic dysfunction in schizophrenia and mood disorders as reflected by decreased levels of glutamic acid decarboxylase 65 and 67 kDa and Reelin proteins in cerebellum. Schizophr. Res. 72 (2-3): 109–22.
- ↑ 91.0 91.1 Veldic M, Kadriu B, Maloku E, Agis-Balboa RC, Guidotti A, Davis JM, Costa E (March 2007). Epigenetic mechanisms expressed in basal ganglia GABAergic neurons differentiate schizophrenia from bipolar disorder. Schizophr. Res. 91 (1-3): 51–61.
- ↑ Eastwood SL, Harrison PJ (September 2003). Interstitial white matter neurons express less reelin and are abnormally distributed in schizophrenia: towards an integration of molecular and morphologic aspects of the neurodevelopmental hypothesis. Mol. Psychiatry 8 (9): 769, 821–31.
- ↑ Abdolmaleky HM, Cheng KH, Russo A, et al (April 2005). Hypermethylation of the reelin (RELN) promoter in the brain of schizophrenic patients: a preliminary report. Am. J. Med. Genet. B Neuropsychiatr. Genet. 134B (1): 60–6.
- ↑ Fatemi SH, Kroll JL, Stary JM (October 2001). Altered levels of Reelin and its isoforms in schizophrenia and mood disorders. Neuroreport 12 (15): 3209–15.
- ↑ Knable MB, Torrey EF, Webster MJ, Bartko JJ (July 2001). Multivariate analysis of prefrontal cortical data from the Stanley Foundation Neuropathology Consortium. Brain Res. Bull. 55 (5): 651–9.
- ↑ Grayson DR, Jia X, Chen Y, et al (June 2005). Reelin promoter hypermethylation in schizophrenia. Proc. Natl. Acad. Sci. U.S.A. 102 (26): 9341–6.
- ↑ Dong E, Agis-Balboa RC, Simonini MV, Grayson DR, Costa E, Guidotti A (August 2005). Reelin and glutamic acid decarboxylase67 promoter remodeling in an epigenetic methionine-induced mouse model of schizophrenia. Proc. Natl. Acad. Sci. U.S.A. 102 (35): 12578–83.
- ↑ Pollin W, Cardon PV, Kety SS (January 1961). Effects of amino acid feedings in schizophrenic patients treated with iproniazid. Science (journal) 133: 104–5.
- ↑ Brune GG, Himwich HE (May 1962). Effects of methionine loading on the behavior of schizophrenic patients. J. Nerv. Ment. Dis. 134: 447–50.
- ↑ Park L, Baldessarini RJ, Kety SS (April 1965). Effects of methionine ingestion in chronic schizophrenia patients treated with monoamine oxidase inhibitors. Arch. Gen. Psychiatry 12: 346–51.
- ↑ Antun FT, Burnett GB, Cooper AJ, Daly RJ, Smythies JR, Zealley AK (June 1971). The effects of L-methionine (without MAOI) in schizophrenia. J Psychiatr Res 8 (2): 63–71.
- ↑ Ruzicka WB, Zhubi A, Veldic M, Grayson DR, Costa E, Guidotti A (April 2007). Selective epigenetic alteration of layer I GABAergic neurons isolated from prefrontal cortex of schizophrenia patients using laser-assisted microdissection. Mol. Psychiatry 12 (4): 385–97.
- ↑ Veldic M, Caruncho HJ, Liu WS, Davis J, Satta R, Grayson DR, Guidotti A, Costa E (January 2004). DNA-methyltransferase 1 mRNA is selectively overexpressed in telencephalic GABAergic interneurons of schizophrenia brains. Proc. Natl. Acad. Sci. U.S.A. 101 (1): 348–53.
- ↑ Veldic M, Guidotti A, Maloku E, Davis JM, Costa E (February 2005). In psychosis, cortical interneurons overexpress DNA-methyltransferase 1. Proc. Natl. Acad. Sci. U.S.A. 102 (6): 2152–7.
- ↑ Tremolizzo L, Doueiri MS, Dong E, et al (March 2005). Valproate corrects the schizophrenia-like epigenetic behavioral modifications induced by methionine in mice. Biol. Psychiatry 57 (5): 500–9.
- ↑ Chen Y, Sharma RP, Costa RH, Costa E, Grayson DR (July 2002). On the epigenetic regulation of the human reelin promoter. Nucleic Acids Res. 30 (13): 2930–9.
- ↑ Mitchell CP, Chen Y, Kundakovic M, Costa E, Grayson DR (April 2005). Histone deacetylase inhibitors decrease reelin promoter methylation in vitro. J. Neurochem. 93 (2): 483–92.
- ↑ Tremolizzo L, Carboni G, Ruzicka WB, et al (December 2002). An epigenetic mouse model for molecular and behavioral neuropathologies related to schizophrenia vulnerability. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 17095–100.
- ↑ Benes FM, Lim B, Matzilevich D, Walsh JP, Subburaju S, Minns M (June 2007). Regulation of the GABA cell phenotype in hippocampus of schizophrenics and bipolars. Proc. Natl. Acad. Sci. U.S.A. 104 (24): 10164–9.
- ↑ Dong E, Guidotti A, Grayson DR, Costa E (March 2007). Histone hyperacetylation induces demethylation of reelin and 67-kDa glutamic acid decarboxylase promoters. Proc. Natl. Acad. Sci. U.S.A. 104 (11): 4676–81.
- ↑ Kundakovic M, Chen Y, Costa E, Grayson DR (March 2007). DNA methyltransferase inhibitors coordinately induce expression of the human reelin and glutamic acid decarboxylase 67 genes. Mol. Pharmacol. 71 (3): 644–53.
- ↑ Kundakovic M, Chen Y, Guidotti A, Grayson DR (November 2008). The reelin and GAD67 promoters are activated by epigenetic drugs that facilitate the disruption of local repressor complexes. Mol. Pharmacol..
- ↑ Guidotti A, Ruzicka W, Grayson DR, et al (January 2007). S-adenosyl methionine and DNA methyltransferase-1 mRNA overexpression in psychosis. Neuroreport 18 (1): 57–60.
- ↑ Fatemi SH, Emamian ES, Kist D, Sidwell RW, Nakajima K, Akhter P, Shier A, Sheikh S, Bailey K (March 1999). Defective corticogenesis and reduction in Reelin immunoreactivity in cortex and hippocampus of prenatally infected neonatal mice. Mol. Psychiatry 4 (2): 145–54.
- ↑ Meyer U, Nyffeler M, Yee BK, Knuesel I, Feldon J (2007). Adult brain and behavioral pathological markers of prenatal immune challenge during early/middle and late fetal development in mice. Brain Behav Immun 22: 469.
- ↑ 116.0 116.1 Wedenoja J, Loukola A, Tuulio-Henriksson A, Paunio T, Ekelund J, Silander K, Varilo T, Heikkilä K, Suvisaari J, Partonen T, Lönnqvist J, Peltonen L (2007). Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families. Mol Psychiatry 13: 673.
- ↑ Shifman S, Johannesson M, Bronstein M, Chen SX, Collier DA, Craddock NJ, Kendler KS, Li T, O'Donovan M, O'Neill FA, Owen MJ, Walsh D, Weinberger DR, Sun C, Flint J, Darvasi A (2008). Genome-Wide Association Identifies a Common Variant in the Reelin Gene That Increases the Risk of Schizophrenia Only in Women. PLoS Genet. 4 (2): e28. free full text
- ↑ Gregório SP, Sallet PC, Do KA, Lin E, Gattaz WF, Dias-Neto E (December 2008). Polymorphisms in genes involved in neurodevelopment may be associated with altered brain morphology in schizophrenia: Preliminary evidence. Psychiatry Res.
- ↑ 119.0 119.1 Suzuki K, Nakamura K, Iwata Y, Sekine Y, Kawai M, Sugihara G, Tsuchiya KJ, Suda S, Matsuzaki H, Takei N, Hashimoto K, Mori N (2007). Decreased expression of reelin receptor VLDLR in peripheral lymphocytes of drug-naive schizophrenic patients. Schizophrenia Research 98: 148.
- ↑ Sweet RA, Henteleff RA, Zhang W, Sampson AR, Lewis DA (May 2008). Reduced Dendritic Spine Density in Auditory Cortex of Subjects with Schizophrenia. Neuropsychopharmacology.
- ↑ Glantz LA, Lewis DA (January 2000). Decreased dendritic spine density on prefrontal cortical pyramidal neurons in schizophrenia. Arch. Gen. Psychiatry 57 (1): 65–73.
- ↑ Rodriguez MA, Pesold C, Liu WS, et al (March 2000). Colocalization of integrin receptors and reelin in dendritic spine postsynaptic densities of adult nonhuman primate cortex. Proc. Natl. Acad. Sci. U.S.A. 97 (7): 3550–5.
- ↑ Costa E, Davis J, Grayson DR, Guidotti A, Pappas GD, Pesold C (October 2001). Dendritic spine hypoplasticity and downregulation of reelin and GABAergic tone in schizophrenia vulnerability. Neurobiol. Dis. 8 (5): 723–42.
- ↑ Kamnasaran D, Muir WJ, Ferguson-Smith MA, Cox DW (May 2003). Disruption of the neuronal PAS3 gene in a family affected with schizophrenia. J. Med. Genet. 40 (5): 325–32.
- ↑ Erbel-Sieler C, Dudley C, Zhou Y, et al (September 2004). Behavioral and regulatory abnormalities in mice deficient in the NPAS1 and NPAS3 transcription factors. Proc. Natl. Acad. Sci. U.S.A. 101 (37): 13648–53.
- ↑ Chen Z, Schwahn BC, Wu Q, He X, Rozen R (August 2005). Postnatal cerebellar defects in mice deficient in methylenetetrahydrofolate reductase. Int. J. Dev. Neurosci. 23 (5): 465–74.
- ↑ Gene Overview of All Published Schizophrenia-Association Studies for GRIN2B - Schizophrenia Gene Database.
- ↑ Podhorna J, Didriksen M (August 2004). The heterozygous reeler mouse: behavioural phenotype. Behav. Brain Res. 153 (1): 43–54.
- ↑ Devlin B, Bennett P, Dawson G, Figlewicz DA, Grigorenko EL, McMahon W, Minshew N, Pauls D, Smith M, Spence MA, Rodier PM, Stodgell C, Schellenberg GD; CPEA GeneticsDevlin B, Bennett P, Dawson G, et al (April 2004). Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network. Am. J. Med. Genet. B Neuropsychiatr. Genet. 126B (1): 46–50.
- ↑ Li J, Nguyen L, Gleason C, et al (April 2004). Lack of evidence for an association between WNT2 and RELN polymorphisms and autism. Am. J. Med. Genet. B Neuropsychiatr. Genet. 126B (1): 51–7.
- ↑ Dutta S, Sinha S, Ghosh S, Chatterjee A, Ahmed S, Usha R (August 2008). Genetic analysis of reelin gene (RELN) SNPs: No association with autism spectrum disorder in the Indian population. Neurosci. Lett. 441 (1): 56–60.
- ↑ Serajee FJ, Zhong H, Mahbubul Huq AH (January 2006). Association of Reelin gene polymorphisms with autism. Genomics 87 (1): 75–83.
- ↑ Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, DeLong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA (June 2005). Analysis of the RELN gene as a genetic risk factor for autism. Mol. Psychiatry 10 (6): 563–71.
- ↑ Fatemi SH, Stary JM, Halt AR, Realmuto GR (December 2001). Dysregulation of Reelin and Bcl-2 proteins in autistic cerebellum. J Autism Dev Disord 31 (6): 529–35.
- ↑ Fatemi SH, Stary JM, Egan EA (April 2002). Reduced blood levels of reelin as a vulnerability factor in pathophysiology of autistic disorder. Cell. Mol. Neurobiol. 22 (2): 139–52.
- ↑ Haas CA, Dudeck O, Kirsch M, et al (July 2002). Role for reelin in the development of granule cell dispersion in temporal lobe epilepsy. J. Neurosci. 22 (14): 5797–802.
- ↑ Heinrich C, Nitta N, Flubacher A, et al (April 2006). Reelin deficiency and displacement of mature neurons, but not neurogenesis, underlie the formation of granule cell dispersion in the epileptic hippocampus. J. Neurosci. 26 (17): 4701–13.
- ↑ Gong C, Wang TW, Huang HS, Parent JM (February 2007). Reelin regulates neuronal progenitor migration in intact and epileptic hippocampus. J. Neurosci. 27 (8): 1803–11.
- ↑ Müller MC, Osswald M, Tinnes S, Häussler U, Jacobi A, Förster E, Frotscher M, Haas CA (January 2009). Exogenous reelin prevents granule cell dispersion in experimental epilepsy. Exp. Neurol..
- ↑ Botella-López A, Burgaya F, Gavín R, et al (April 2006). Reelin expression and glycosylation patterns are altered in Alzheimer's disease. Proc. Natl. Acad. Sci. U.S.A. 103 (14): 5573–8.
- ↑ Wirths O, Multhaup G, Czech C, et al (December 2001). Reelin in plaques of beta-amyloid precursor protein and presenilin-1 double-transgenic mice. Neurosci. Lett. 316 (3): 145–8.
- ↑ Seripa D, Matera MG, Franceschi M, et al (July 2008). The RELN locus in Alzheimer's disease. J. Alzheimers Dis. 14 (3): 335–44.
- ↑ Baloyannis SJ (July 2005). Morphological and morphometric alterations of Cajal-Retzius cells in early cases of Alzheimer's disease: a Golgi and electron microscope study. Int. J. Neurosci. 115 (7): 965–80.
- ↑ Baloyannis SJ, Costa V, Mauroudis I, Psaroulis D, Manolides SL, Manolides LS (April 2007). Dendritic and spinal pathology in the acoustic cortex in Alzheimer's disease: morphological and morphometric estimation by Golgi technique and electron microscopy. Acta Otolaryngol. 127 (4): 351–4.
- ↑ Aoki, Takeya; Mizuki, Yasushi; Terashima, Toshio Relation between schizophrenia and Alzheimer's disease: the reelin signaling pathway Psychogeriatrics, Volume 5, Number 2, June 2005 , pp. 42-47(6)
- ↑ Sato N, Fukushima N, Chang R, Matsubayashi H, Goggins M. (2006) Differential and epigenetic gene expression profiling identifies frequent disruption of the RELN pathway in pancreatic cancers. Gastroenterology. 130(2):548-65. PMID 16472607
- ↑ Perrone G, Vincenzi B, Zagami M, Santini D, Panteri R, Flammia G, Verzi A, Lepanto D, Morini S, Russo A, Bazan V, Tomasino RM, Morello V, Tonini G, Rabitti C. (2007) Reelin expression in human prostate cancer: a marker of tumor aggressiveness based on correlation with grade. Modern Pathology. doi:10.1038/modpathol.3800743. PMID 17277764
- ↑ Seigel GM, Hackam AS, Ganguly A, Mandell LM, Gonzalez-Fernandez F (2007). Human embryonic and neuronal stem cell markers in retinoblastoma. Mol. Vis. 13: 823–32.
- ↑ Schrauwen I, Ealy M, Huentelman MJ, Thys M, Homer N, Vanderstraeten K, Fransen E, Corneveaux JJ, Craig DW, Claustres M, Cremers CW, Dhooge I, Van de Heyning P, Vincent R, Offeciers E, Smith RJ, Van Camp G (February 2009). A Genome-wide Analysis Identifies Genetic Variants in the RELN Gene Associated with Otosclerosis. Am. J. Hum. Genet..
- ↑ Dong E, Nelson M, Grayson DR, Costa E, Guidotti A (August 2008). Clozapine and sulpiride but not haloperidol or olanzapine activate brain DNA demethylation. Proc. Natl. Acad. Sci. U.S.A..
- The book: Fatemi, S. Hossein (2008). Reelin Glycoprotein: Structure, Biology and Roles in Health and Disease, 444 pages, Berlin: Springer.
- A review: Förster E, Jossin Y, Zhao S, Chai X, Frotscher M, Goffinet AM (February 2006). Recent progress in understanding the role of Reelin in radial neuronal migration, with specific emphasis on the dentate gyrus. Eur. J. Neurosci. 23 (4): 901–9.
Articles, publications, webpagesEdit
Figures and imagesEdit
- Reelin gene expression in mice. Brain Gene Expression Map. St. Jude Children’s Research Hospital. URL accessed on 2008-08-23.
- Schematic representation of signaling through the LDLR family members apoER2 and VLDL receptor. URL accessed on 2008-08-23. – A figure from Beffert U, Stolt PC, Herz J (March 2004). Functions of lipoprotein receptors in neurons. J. Lipid Res. 45 (3): 403–9.
- Proposed mechanism by which mouse RELN promoter regulate reelin gene expression. Proc. Natl. Acad. Sci. USA. URL accessed on 2008-08-23. – A figure from Dong E, Agis-Balboa RC, Simonini MV, Grayson DR, Costa E, Guidotti A (August 2005). Reelin and glutamic acid decarboxylase67 promoter remodeling in an epigenetic methionine-induced mouse model of schizophrenia. Proc. Natl. Acad. Sci. U.S.A. 102 (35): 12578–83.
- Corticogenesis in wild-type, reeler mutant and β1 deficient mice. URL accessed on 2008-08-23. – A figure from Magdaleno SM, Curran T (December 2001). Brain development: integrins and the Reelin pathway. Curr. Biol. 11 (24): R1032–5.
- Effects of human and naturally occurring mouse RELN mutations on the predicted protein.. Nature Genetics. URL accessed on 2008-08-23. A figure from Hong SE, Shugart YY, Huang DT, et al (September 2000). Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. Nat. Genet. 26 (1): 93–6.
- MRI analysis of chromosome 7q22-linked lissencephaly with cerebellar hypoplasia.. Nature Genetics. URL accessed on 2008-08-23. – A figure from Hong et al.
Hydrolase: proteases (EC 3.4)
Angiotensin-converting enzyme - Dipeptidase - Dipeptidyl peptidase-4 - DD-transpeptidase
|This page uses Creative Commons Licensed content from Wikipedia (view authors).|