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File:RatBarrelFieldCOstain.jpg
The barrel cortex refers to the dark-staining regions of layer four of the somatosensory cortex where somatosensory inputs from the contralateral side of the body come in from the thalamus. Barrels are found in some species of rodents and species of at least two other orders.[1] The rest of this article will focus on the 'whisker barrels' in the somatosensory cortex of rodents. Inputs from the thalamus carrying information from a given whisker terminate in discrete areas of layer IV forming anatomically distinguishable areas (barrels) which are separated from each other by areas called septa. These structures were first discovered by Woolsey and Van der Loos (1970).[2] Recognizing that the array was similar to that of the vibrissae on the mystacial pad, they hypothesized that the barrels were the "cortical correlates of the mystacial vibrissae" and that "one barrel represents one vibrissa".

Due to its distinctive cytoarchitectonics and functional significance, the barrel cortex has played an important role in neuroscience. The majority of what is known about corticothalamic processing comes from studying the barrel cortex and researchers have intensively studied the barrel cortex as a model of neocortical column.

Neurons within the layer IV barrel cortex directly code for whisker displacement. That is to say, that the neuron within a given barrel will fire when the whisker that barrel represents is moved. These neurons also show directional sensitivity, certain neurons will only fire when the whisker is moved in a specific direction.[3][4]

Neurons in the barrel cortex exhibit the property of synaptic plasticity that allows them to alter the vibrissae to which they respond depending on the rodent's history of tactile experience.[5] The field of barrel cortex research has matured to the stage where a book has been published on the subject.[6]

The Posteromedial Barrel Subfield Edit

File:Labeled40xVibrissae.jpg

The posteromedial barrel subfield (PMBSF) is a highly consistent region of the barrel field (Woolsey, 1978). Barrels of the PMBSF are the largest and most elliptical in shape and have a striking topographical organization that is identical to that of the major facial whiskers (also called myastacial vibrissae); these whiskers are organized into 5 rows of 4-7 large whiskers that run close to parallel with the bridge of the nose. (Woolsey and Van der Loos, 1970). A consideration of this morphology led Woolsey and Van der Loos to propose that the barrels of the PMBSF were the cortical correlates of the myastacial vibrissae; this is sometimes called the one-barrel-one-vibrissa hypothesis (Woolsey and Van der Loos, 1970). Thus each barrel in the PMBSF is thought to correspond with a single myastacial vibrissa on the contralateral side of the animal. In 1973 Woolsey and Van der Loos provided strong evidence for this hypothesis by selectively damaging individual whiskers in rodents at birth and noticing that when the brains of these animals were analyzed the corresponding barrel was not present.

Afferent pathwaysEdit

File:Barrel cortex pathways.jpg
Sensory information flows from whisker follicles to somatosensory cortex through at least three parallel pathways. The trigeminal nerve carries afferent fibres from the follicles into the brainstem where they synapse with neurons in four different nuclei: principal, interpolar, oral, and caudal. The most important of these pathways for our purposes is the lemniscal pathway, in which axons from the principal nucleus cross over and project to “barreloids” in the dorsomedial section of the ventroposterior medial nucleus (VPMdm) of the thalamus. Neurons in VPMdm project mainly to barrels in layer 4 of primary somatosensory cortex (S1). In the extralemniscal pathway, neurons of the interpolar nucleus project to the ventrolateral section of the VPM (VPMvl). Neurons in VPMvl project to septa between the barrels and to secondary somatosensory cortex (S2). The paralemniscal pathway runs via the interpolar nucleus and the posterior nucleus (POm) of the thalamus to S2 and to diffuse targets in barrel cortex especially layer 5. These different pathways are thought to transmit different modalities of sensory information from the whisker.[7][8]

Barrel cortex as an experimental systemEdit

The barrel cortex of the rodent has proved to be a fruitful model system for investigating plasticity in primary somatosensory cortex (S1). There are several reasons for its popularity (adapted from Feldman and Brecht, 2005 [9]):

  1. The barrel cortex contains an orderly map which corresponds with the arrangement of the facial whiskers.
  2. The cortical representations of the whiskers correspond one-to-one with barrel structures which are visible under the microscope even in unstained slices.
  3. Barrel cortex is superficially located and so amenable to in vivo investigation.
  4. Sensory deprivation, by trimming or plucking of whiskers, or stimulation, by whisker vibration, is easy to arrange experimentally.
  5. The use of transgenic mice allows genetic and molecular mechanisms of plasticity to be investigated.
  6. Barrel columns are a specialized example of cortical columns, which are believed to be an important feature of cortical functional organization, suggesting that results from barrel cortex may be generally applicable to the rest of the sensory cortex.[2][10]

Experience-dependent plasticityEdit

Experience-dependent plasticity is commonly studied in the barrel cortex by partially depriving it of sensory input, either by lesioning elements of the afferent pathway (e.g. the trigeminal nerve) or by ablating, plucking, or trimming some of the facial whiskers. Only lesioning affects the anatomical structure of the barrels, but innocuous forms of deprivation can induce rapid changes in the cortical map into adulthood, without any corresponding changes in the barrel structures.[11] These two paradigms seem to work by different mechanisms.

Some forms of plasticity in the barrel cortex display a critical period. Plucking whiskers in neonatal rats causes a long-lasting expansion of the representation of the spared whisker in layer 4.[12] However, layer 4 plasticity rapidly diminishes if sensory deprivation begins after day 4 of life (P4) whereas representations in layer 2/3 remain highly plastic into adulthood.[13][14]

Two cortical processes run alongside each other when barrel cortex is deprived of sensory input from some whiskers to produce representational plasticity. In deprived cortex neuronal responses to spared whiskers are enhanced, and responses to deprived whiskers are weakened. These two processes have different time courses, with the weakening of deprived response preceding the strengthening of spared response, implying that they have different underlying mechanisms. These two effects combine to produce an expansion of the cortical representation of spared whiskers into the representation of adjacent deprived whiskers.[9][13]

It is likely that several different mechanisms are involved in producing experience-dependent plasticity in a whisker deprivation protocol (adapted from Feldman and Brecht, 2005 [9]):

  1. There is an immediate unmasking effect, where loss of input to a deprived barrel column leads to a loss of inhibitory firing in that column which unmasks horizontal excitatory connections from adjacent spared columns.[15] This does not explain longer-lasting plastic changes as the unmasking would disappear immediately if the deprived input was reinstated (for example by allowing the whisker to regrow).
  2. The involvement of LTP- and LTD-like processes is suggested by the observation that plasticity can be compromised by interfering with expression of calmodulin-dependent protein kinase II (CaMKII) or cyclic-AMP response element binding protein (CREB) in transgenic mice.[16][17] Spike timing rather than frequency may be an important factor. Associative LTP has been demonstrated at layer 4 to layer 2/3 synapses when the layer 4 neuron fires 0-15 ms before the layer 2/3 neuron, and LTD is observed when this timing order is reversed.[18] Such mechanisms could act rapidly to produce plastic changes within hours or days.
  3. Sensory deprivation has been demonstrated to cause changes in synaptic dynamics such as EPSP amplitude and frequency. The net effect of these changes is to increase the proportion of synaptic input which layer 2/3 neurons in deprived barrels receive from spared barrels.[19] These observations suggest that other, more specific, mechanisms besides LTP/LTD are at play in experience-dependent plasticity.
  4. It seems intuitively likely that structural changes at the level of axons, dendrite branches, and dendrite spines underlie some of the long-term plastic changes in the cortex. Axonal remodelling has been reported in lesion-induced plasticity but not (until now) in experience-dependent plasticity,[20] but a recent study by Cheetham et al.[21] found that whisker trimming produces targeted axonal remodelling in spared cortex. Dendritic branching is important during prenatal and neonatal development, is involved in plasticity induced by lesions, but is not involved in experience-dependent plasticity.[22] In vivo two-photon microscopy reveals that dendritic spines in mouse barrel cortex are highly dynamic and subject to continuous turnover, and may be associated with formation or deletion of synapses.[22] It is likely that spine turnover is necessary but not sufficient to produce experience-dependent plasticity, and other mechanisms such as axonal remodelling are also needed to explain features such as savings from prior experience.[21]

ReferencesEdit

  1. Woolsey TA, Welker C, Schwartz RH. Comparative anatomical studies of the SmL face cortex with special reference to the occurrence of "barrels" in layer IV.. The Journal of Comparative Neurology 164 (1): 79–94.
  2. 2.0 2.1 Woosley, T.A., Van Der Loos, H. 1970. The structural organization of layer IV in the somatosensory region (SI) of mouse cerebral cortex: The description of a cortical field composed of discrete cytoarchitectonic units. Brain Research. 205-238.
  3. Swadlow HA. Efferent neurons and suspected interneurons in S-1 vibrissa cortex of the awake rabbit: receptive fields and axonal properties. J Neurophysiol 62: 288–308, 1989
  4. Swadlow HA. Efferent neurons and suspected interneurons in second somatosensory cortex of the awake rabbit: receptive fields and axonal properties. J Neurophysiol 66: 1392–1409, 1991
  5. Hardingham N, Glazewski S, Pakhotin P, Mizuno K, Chapman PF, Giese KP, Fox K. Neocortical long-term potentiation and experience-dependent synaptic plasticity require alpha-calcium/calmodulin-dependent protein kinase II auto-phosphorylation. J Neurosci. 2003 Jun 1;23(11):4428-36.
  6. Fox, K. Barrel Cortex. Cambridge, New York, Melbourne. Cambridge University Press. 2008. ISBN 978-0-521-85217-3
  7. Diamond ME, von Heimendahl M, Knutsen PM, Kleinfeld D, Ahissar E (2008) 'Where' and 'what' in the whisker sensorimotor system. Nat Rev Neurosci 9:601-612.
  8. Fox K (2008) Anatomical pathways. In: Barrel cortex. pp14-48. Cambridge, UK: Cambridge University Press.
  9. 9.0 9.1 9.2 Feldman DE, Brecht M (2005) Map plasticity in somatosensory cortex. Science 310:810-815.
  10. Mountcastle VB (1957) Modality and topographic properties of single neurons of cat's somatic sensory cortex. J Neurophysiol 20:408-434.
  11. Fox K (2002) Anatomical pathways and molecular mechanisms for plasticity in the barrel cortex.Neuroscience 111:799-814.
  12. Fox K (1992) A critical period for experience-dependent synaptic plasticity in rat barrel cortex. J Neurosci 12:1826-1838.
  13. 13.0 13.1 Glazewski S, Fox K (1996) Time course of experience-dependent synaptic potentiation anddepression in barrel cortex of adolescent rats. J Neurophysiol 75:1714-1729.
  14. Stern EA, Maravall M, Svoboda K (2001) Rapid development and plasticity of layer 2/3 maps in rat barrel cortex in vivo. Neuron 31:305-315.
  15. Kelly MK, Carvell GE, Kodger JM, Simons DJ (1999) Sensory loss by selected whisker removal produces immediate disinhibition in the somatosensory cortex of behaving rats. J Neurosci 19:9117-9125.
  16. Glazewski S, Chen CM, Silva A, Fox K (1996) Requirement for alpha-CaMKII in experience dependent plasticity of the barrel cortex. Science 272:421-423.
  17. Glazewski S, Barth AL, Wallace H, McKenna M, Silva A, Fox K (1999) Impaired experiencedependent plasticity in barrel cortex of mice lacking the alpha and delta isoforms of CREB. Cereb Cortex 9:249-256.
  18. Feldman DE (2000) Timing-based LTP and LTD at vertical inputs to layer II/III pyramidal cells inrat barrel cortex. Neuron 27:45-56.
  19. Finnerty GT, Roberts LS, Connors BW (1999) Sensory experience modifies the short-term dynamics of neocortical synapses. Nature 400:367-371.
  20. Chklovskii DB, Mel BW, Svoboda K (2004) Cortical rewiring and information storage. Nature 431:782-788.
  21. 21.0 21.1 Cheetham CE, Hammond MS, MacFarlane R, Finnerty GT (2008) Altered sensory experience induces targeted rewiring of local excitatory connections in mature neocortex. J Neurosci (in press).
  22. 22.0 22.1 Trachtenberg JT, Chen BE, Knott GW, Feng G, Sanes JR, Welker E, Svoboda K (2002) Long-term in vivo imaging of experience-dependent synaptic plasticity in adult cortex. Nature 420:788-794.

External linksEdit

Research groups working on barrel cortex:

Books on barrel cortex

Barrel Cortex book
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