Open main menu

The cerebral cortex is the outer layer of neural tissue of the cerebrum of the brain, in humans and other mammals. It is separated into two cortices, by the longitudinal fissure that divides the cerebrum into the left and right cerebral hemispheres. The two hemispheres are joined beneath the cortex by the corpus callosum. The cerebral cortex is the largest site of neural integration in the central nervous system.[1] It plays a key role in memory, attention, perception, awareness, thought, language, and consciousness.

Cerebral cortex
Tissue slice from the brain of an adult macaque monkey (Macaca mulatta). The cerebral cortex is the outer layer depicted in dark violet. Source:
Golgi-stained neurons in the cortex
Part ofCerebrum
LatinCortex cerebri
NeuroLex IDbirnlex_1494
Anatomical terms of neuroanatomy

In large mammals, the cerebral cortex is folded, providing a greater surface area in the confined volume of the cranium. Apart from minimising brain and cranial volume, cortical folding is crucial for the wiring of the brain and its functional organisation. In mammals with a small brain there is no folding and the cortex is smooth.[2][3]

A fold or ridge in the cortex is termed a gyrus (plural gyri) and a groove is termed a sulcus (plural sulci). These surface convolutions appear during fetal development and continue to mature after birth through the process of gyrification. In the human brain the majority of the cerebral cortex is not visible from the outside, but buried in the sulci.[4]

The cerebral cortex contains a large number of neuronal and glial cell bodies, as well as their intricate dendritic formations and axonal projections, which connect at synapses to form basic functional circuits.[4] The cerebral cortex is entirely made of gray matter, contrasting with the underlying white matter, which consists mainly of axons traveling to and from the cortex, their myelinated sheaths, and the cell bodies of oligodendrocytes.[4]



The cerebral cortex is the outer covering of the surfaces of the cerebral hemispheres and is folded into peaks called gyri, and grooves called sulci. It is between two and three millimetres thick.[1] It makes up 40 per cent of the brain's mass. There are between 14 and 16 billion neurons in the cortex.[1]


The cerebral cortex is folded in a way that allows a large surface area of neural tissue to fit within the confines of the neurocranium. When unfolded, each hemispheric cortex has a total surface area of about 1.3 square feet (0.12 m2).[5] The folding is inward away from the surface of the brain, and is also present on the medial surface of each hemisphere within the longitudinal fissure. Most mammals have a cerebral cortex that is convoluted with the peaks known as gyri and the troughs or grooves known as sulci. Some small mammals such as rodents have smooth cerebral surfaces without gyrification.[3]


For species of mammals, larger brains (in absolute terms, not just in relation to body size) tend to have thicker cortices.[6] The smallest mammals, such as shrews, have a neocortical thickness of about 0.5 mm; the ones with the largest brains, such as humans and fin whales, have thicknesses of 2.3–2.8 mm. There is an approximately logarithmic relationship between brain weight and cortical thickness.[6]Magnetic resonance imaging of the brain (MRI) makes it possible to get a measure for the thickness of the human cerebral cortex and relate it to other measures. The thickness of different cortical areas varies but in general, sensory cortex is thinner than motor cortex.[7] One study has found some positive association between the cortical thickness and intelligence.[8] Another study has found that the somatosensory cortex is thicker in migraine sufferers, though it is not known if this is the result of migraine attacks or the cause of them.[9][10] A later study using a larger patient population reports no change in the cortical thickness in migraine sufferers.[11] A genetic disorder of the cerebral cortex, whereby decreased folding in certain areas results in a microgyrus, where there are four layers instead of six, is in some instances seen to be related to dyslexia.[12]


Cerebral cortex. (Poirier.) To the left, the groups of cells; to the right, the systems of fibers. Quite to the left of the figure a sensory nerve fiber is shown. Cell body layers are labeled on the left, and fiber layers are labeled on the right.
Three drawings of cortical lamination by Santiago Ramon y Cajal, each showing a vertical cross-section, with the surface of the cortex at the top. Left: Nissl-stained visual cortex of a human adult. Middle: Nissl-stained motor cortex of a human adult. Right: Golgi-stained cortex of a ​1 12 month old infant. The Nissl stain shows the cell bodies of neurons; the Golgi stain shows the dendrites and axons of a random subset of neurons.
Micrograph showing the visual cortex (predominantly pink). Subcortical white matter (predominantly blue) is seen at the bottom of the image. HE-LFB stain.

The different cortical layers each contain a characteristic distribution of neuronal cell types and connections with other cortical and subcortical regions. There are direct connections between different cortical areas and indirect connections via the thalamus, for example. One of the clearest examples of cortical layering is the line of Gennari in the primary visual cortex. This is a band of whiter tissue that can be observed with the naked eye in the fundus of the calcarine sulcus of the occipital lobe. The line of Gennari is composed of axons bringing visual information from the thalamus into layer four of the visual cortex.

Staining cross-sections of the cortex to reveal the position of neuronal cell bodies and the intracortical axon tracts allowed neuroanatomists in the early 20th century to produce a detailed description of the laminar structure of the cortex in different species. After the work of Korbinian Brodmann (1909) the neurons of the cerebral cortex are grouped into six main layers, from outside (pial surface) to inside (white matter):

  1. Layer I, the molecular layer, contains few scattered neurons, including GABAergic rosehip neurons,[13] and consists largely of extensions of apical dendritic tufts of pyramidal neurons and horizontally oriented axons, as well as glial cells.[14] During development Cajal-Retzius[15] and subpial granular layer cells[16] are present in this layer. Also, some spiny stellate cells can be found here. Inputs to the apical tufts are thought to be crucial for the feedback interactions in the cerebral cortex involved in associative learning and attention.[17] While it was once thought that the input to layer I came from the cortex itself,[18] it is now realized that layer I across the cerebral cortex mantle receives substantial input from matrix or M-type thalamus cells[19] (in contrast to core or C-type that go to layer IV).[20]
  2. Layer II, the external granular layer, contains small pyramidal neurons and numerous stellate neurons.
  3. Layer III, the external pyramidal layer, contains predominantly small and medium-size pyramidal neurons, as well as non-pyramidal neurons with vertically oriented intracortical axons; layers I through III are the main target of interhemispheric corticocortical afferents, and layer III is the principal source of corticocortical efferents.
  4. Layer IV, the internal granular layer, contains different types of stellate and pyramidal cells, and is the main target of thalamocortical afferents from thalamus type C neurons[20] as well as intra-hemispheric corticocortical afferents. The layers above layer IV are also referred to as supragranular layers (layers I-III), whereas the layers below are referred to as infragranular layers (layers V and VI).
  5. Layer V, the internal pyramidal layer, contains large pyramidal neurons which give rise to axons leaving the cortex and running down to subcortical structures (such as the basal ganglia). In the primary motor cortex of the frontal lobe, layer V contains giant pyramidal cells called Betz cells, whose axons travel through the internal capsule, the brain stem and the spinal cord forming the corticospinal tract, which is the main pathway for voluntary motor control.
  6. Layer VI, the polymorphic or multiform layer, contains few large pyramidal neurons and many small spindle-like pyramidal and multiform neurons; layer VI sends efferent fibers to the thalamus, establishing a very precise reciprocal interconnection between the cortex and the thalamus.[21] That is, layer VI neurons from one cortical column connect with thalamus neurons that provide input to the same cortical column. These connections are both excitatory and inhibitory. Neurons send excitatory fibers to neurons in the thalamus and also send collaterals to the thalamic reticular nucleus that inhibit these same thalamus neurons or ones adjacent to them.[22] One theory is that because the inhibitory output is reduced by cholinergic input to the cerebral cortex, this provides the brainstem with adjustable "gain control for the relay of lemniscal inputs".[22]


The cortical layers are not simply stacked one over the other; there exist characteristic connections between different layers and neuronal types, which span all the thickness of the cortex. These cortical microcircuits are grouped into cortical columns and minicolumns. It has been proposed that the minicolumns are the basic functional units of the cortex.[23] In 1957, Vernon Mountcastle showed that the functional properties of the cortex change abruptly between laterally adjacent points; however, they are continuous in the direction perpendicular to the surface. Later works have provided evidence of the presence of functionally distinct cortical columns in the visual cortex (Hubel and Wiesel, 1959),[24] auditory cortex, and associative cortex.

Cortical areas that lack a layer IV are called agranular. Cortical areas that have only a rudimentary layer IV are called dysgranular.[25] Information processing within each layer is determined by different temporal dynamics with that in the layers II/III having a slow 2 Hz oscillation while that in layer V having a fast 10–15 Hz one.[26]

Types of cortexEdit

Based on the differences in lamination the cerebral cortex can be classified into two types, the large area of neocortex and the much smaller area of allocortex:

  • The neocortex (also known as the isocortex or neopallium) is the part of the mature cerebral cortex with six distinct layers. Examples of neocortical areas include the granular primary motor cortex, also known as Brodmann area 4, and the striate primary visual cortex, or Brodmann area 17. The neocortex has two types of cortices, the true isocortex and the proisocortex. The proisocortex contains Brodmann areas 24, 25, and 32
  • The allocortex is the part of the cerebral cortex with less than six layers and has three regions, the paleocortex with three cortical laminae and the archicortex which has four or five, and a transitional area adjacent to the allocortex, the periallocortex. Examples of allocortex are the olfactory cortex and the hippocampus.

There is a transitional area between the neocortex and the allocortex called the paralimbic cortex, where layers 2, 3 and 4 are merged. This area incorporates the proisocortex of the neocortex and the periallocortex of the allocortex. In addition, the cerebral cortex may be classified on the basis of gross topographical conventions into four lobes (named after the four skull bones protecting them): the temporal lobe, the occipital lobe, the parietal lobe, and the frontal lobe.

Brodmann areasEdit

Different parts of the cerebral cortex are involved in different cognitive and behavioral functions. The differences show up in a number of ways: the effects of localized brain damage, regional activity patterns exposed when the brain is examined using functional imaging techniques, connectivity with subcortical areas, and regional differences in the cellular architecture of the cortex. Neuroscientists describe most of the cortex—the part they call the neocortex—as having six layers, but not all layers are apparent in all areas, and even when a layer is present, its thickness and cellular organization may vary. Scientists have constructed maps of cortical areas on the basis of variations in the appearance of the layers as seen with a microscope. One of the most widely used schemes came from Korbinian Brodmann, who split the cortex into 51 different areas and assigned each a number (many of these Brodmann areas have since been subdivided). For example, Brodmann area 1 is the primary somatosensory cortex, Brodmann area 17 is the primary visual cortex, and Brodmann area 25 is the anterior cingulate cortex.[27]

Blood supply and drainageEdit

Cortical blood supply

Blood is supplied to the cerebral cortex via the cerebral circulation.


Human cortical development between 26 and 39 week gestational age

The prenatal development of the cerebral cortex is a complex and finely tuned process called corticogenesis, influenced by the interplay between genes and the environment.[28] The cerebral cortex develops from the most anterior part of the neural plate, a specialized part of the embryonic ectoderm.[29] The neural plate folds and closes to form the neural tube. From the cavity inside the neural tube develops the ventricular system, and, from the epithelial cells of its walls, the neurons and glia of the nervous system. The most anterior (front, or cranial) part of the neural plate, the prosencephalon, which is evident before neurulation begins, gives rise to the cerebral hemispheres and its later cortex.[30]

Cortical neurons are generated within the ventricular zone, next to the ventricles. At first, this zone contains progenitor cells, which divide to produce glial cells and neurons.[31] The glial fibers produced in the first divisions of the progenitor cells are radially oriented, spanning the thickness of the cortex from the ventricular zone to the outer, pial surface, and provide scaffolding for the migration of neurons outwards from the ventricular zone.[32][33] The first divisions of the progenitor cells are symmetric, which duplicates the total number of progenitor cells at each mitotic cycle. Then, some progenitor cells begin to divide asymmetrically, producing one postmitotic cell that migrates along the radial glial fibers, leaving the ventricular zone, and one progenitor cell, which continues to divide until the end of development, when it differentiates into a glial cell or an ependymal cell. As the G1 phase of mitosis is elongated, in what is seen as selective cell-cycle lengthening, the newly-born neurons migrate to more superficial layers of the cortex.[34] The migrating daughter cells become the pyramidal cells of the cerebral cortex.[35] The development process is time ordered and regulated by hundreds of genes and epigenetic regulatory mechanisms.[36]

The layered structure of the mature cerebral cortex is formed during development. The first pyramidal neurons generated migrate out of the ventricular zone and subventricular zone, together with reelin producing Cajal–Retzius neurons, from the preplate. Next, a cohort of neurons migrating into the middle of the preplate divides this transient layer into the superficial marginal zone, which will become layer one of the mature neocortex, and the subplate,[37] forming a middle layer called the cortical plate. These cells will form the deep layers of the mature cortex, layers five and six. Later born neurons migrate radially into the cortical plate past the deep layer neurons, and become the upper layers (two to four). Thus, the layers of the cortex are created in an inside-out order.[38] The only exception to this inside-out sequence of neurogenesis occurs in the layer I of primates, in which, in contrast to rodents, neurogenesis continues throughout the entire period of corticogenesis.[39]

Depicted in blue, Emx2 is highly expressed at the caudomedial pole and dissipates outward. Pax6 expression is represented in purple and is highly expressed at the rostral lateral pole. (Adapted from Sanes, D., Reh, T., & Harris, W. (2012). Development of the Nervous System (3rd ed.). Burlington: Elsevier Science)

The map of functional cortical areas, which include primary motor and visual cortex, originates from a 'protomap',[40] which is regulated by molecular signals such as fibroblast growth factor FGF8 early in embryonic development.[41][42] These signals regulate the size, shape, and position of cortical areas on the surface of the cortical primordium, in part by regulating gradients of transcription factor expression, through a process called cortical patterning. Examples of such transcription factors include the genes EMX2 and PAX6.[43] Together, both transcription factors form an opposing gradient of expression. Pax6 is highly expressed at the rostral lateral pole, while Emx2 is highly expressed in the caudomedial pole. The establishment of this gradient is important for proper development. For example, mutations in Pax6 can cause expression levels of Emx2 to expand out of its normal expression domain, which would ultimately lead to an expansion of the areas normally derived from the caudal medial cortex, such as the visual cortex. On the contrary, if mutations in Emx2 occur, it can cause the Pax6-expressing domain to expand and result in the frontal and motor cortical regions enlarging. Therefore, researchers believe that similar gradients and signaling centers next to the cortex could contribute to the regional expression of these transcription factors.[44]

Two very well studied patterning signals for the cortex include FGF and retinoic acid. If FGFs are misexpressed in different areas of the developing cortex, cortical patterning is disrupted. Specifically, when Fgf8 is increased in the anterior pole, Emx2 is downregulated and a caudal shift in the cortical region occurs. This ultimately causes an expansion of the rostral regions. Therefore, Fgf8 and other FGFs play a role in the regulation of expression of Emx2 and Pax6 and represent how the cerebral cortex can become specialized for different functions.[44]

Rapid expansion of the cortical surface area is regulated by the amount of self-renewal of radial glial cells and is partly regulated by FGF and Notch genes.[45] During the period of cortical neurogenesis and layer formation, many higher mammals begin the process of gyrification, which generates the characteristic folds of the cerebral cortex.[46][47] Gyrification is regulated by a DNA-associated protein Trnp1[48] and by FGF and SHH signaling[49][50]

Neurogenesis is shown in red and lamination is shown in blue. Adapted from (Sur et al. 2001)

The cerebral cortex is composed of a heterogenous population of cells that give rise to different cell types. The majority of these cells are derived from radial glia migration that form the different cell types of the neocortex and it is a period associated with an increase in neurogenesis. Similarly, the process of neurogenesis regulates lamination to form the different layers of the cortex. During this process there is an increase in the restriction of cell fate that begins with earlier progenitors giving rise to any cell type in the cortex and later progenitors giving rise only to neurons of superficial layers. This differential cell fate creates an inside-out topography in the cortex with younger neurons in superficial layers and older neurons in deeper layers. In addition, laminar neurons are stopped in S or G2 phase in order to give a fine distinction between the different cortical layers. Laminar differentiation is not fully complete until after birth since during development laminar neurons are still sensitive to extrinsic signals and environmental cues.[51]

Although the majority of the cells that compose the cortex are derived locally from radial glia there is a subset population of neurons that migrate from other regions. Radial glia give rise to neurons that are pyramidal in shape and use glutamate as a neurotransmitter, however these migrating cells contribute neurons that are stellate-shaped and use GABA as their main neurotransmitter. These GABAergic neurons are generated by progenitor cells in the medial ganglionic eminence (MGE) that migrate tangentially to the cortex via the subventricular zone. This migration of GABAergic neurons is particularly important since GABA receptors are excitatory during development. This excitation is primarily driven by the flux of chloride ions through the GABA receptor, however in adults chloride concentrations shift causing an inward flux of chloride that hyperpolarizes postsynaptic neurons.[44]


Of all the different brain regions, the cerebral cortex shows the largest evolutionary variation and has evolved most recently.[3] In contrast to the highly conserved circuitry of the medulla oblongata, for example, which serves critical functions such as regulation of heart and respiration rates, many areas of the cerebral cortex are not strictly necessary for survival. Thus, the evolution of the cerebral cortex has seen the advent and modification of new functional areas—particularly association areas that do not directly receive input from outside the cortex.[3]

A key theory of cortical evolution is embodied in the radial unit hypothesis and related protomap hypothesis, first proposed by Rakic.[52] This theory states that new cortical areas are formed by the addition of new radial units, which is accomplished at the stem cell level. The protomap hypothesis states that the cellular and molecular identity and characteristics of neurons in each cortical area are specified by cortical stem cells, known as radial glial cells, in a primordial map. This map is controlled by secreted signaling proteins and downstream transcription factors.[53][54][55]


Some functional areas of cortex


The cerebral cortex is connected to various subcortical structures such as the thalamus and the basal ganglia, sending information to them along efferent connections and receiving information from them via afferent connections. Most sensory information is routed to the cerebral cortex via the thalamus. Olfactory information, however, passes through the olfactory bulb to the olfactory cortex (piriform cortex). The majority of connections are from one area of the cortex to another, rather than from subcortical areas; Braitenberg and Schüz (1998) claim that in primary sensory areas, at the cortical level where the input fibres terminate, up to 20% of the synapses are supplied by extracortical afferents but that in other areas and other layers the percentage is likely to be much lower.[56]

Cortical areasEdit

Lateral surface of the human cerebral cortex
Medial surface of the human cerebral cortex

The cortex is commonly described as comprising three parts: sensory, motor, and association areas.

Sensory areasEdit

The sensory areas are the cortical areas that receive and process information from the senses. Parts of the cortex that receive sensory inputs from the thalamus are called primary sensory areas. The senses of vision, audition, and touch are served by the primary visual cortex, primary auditory cortex and primary somatosensory cortex respectively. In general, the two hemispheres receive information from the opposite (contralateral) side of the body. For example, the right primary somatosensory cortex receives information from the left limbs, and the right visual cortex receives information from the left visual field. The organization of sensory maps in the cortex reflects that of the corresponding sensing organ, in what is known as a topographic map. Neighboring points in the primary visual cortex, for example, correspond to neighboring points in the retina. This topographic map is called a retinotopic map. In the same way, there exists a tonotopic map in the primary auditory cortex and a somatotopic map in the primary sensory cortex. This last topographic map of the body onto the posterior central gyrus has been illustrated as a deformed human representation, the somatosensory homunculus, where the size of different body parts reflects the relative density of their innervation. Areas with lots of sensory innervation, such as the fingertips and the lips, require more cortical area to process finer sensation.

Motor areasEdit

The motor areas are located in both hemispheres of the cortex. They are shaped like a pair of headphones stretching from ear to ear. The motor areas are very closely related to the control of voluntary movements, especially fine fragmented movements performed by the hand. The right half of the motor area controls the left side of the body, and vice versa.

Two areas of the cortex are commonly referred to as motor:

In addition, motor functions have been described for:

Just underneath the cerebral cortex are interconnected subcortical masses of grey matter called basal ganglia (or nuclei). The basal ganglia receive input from the substantia nigra of the midbrain and motor areas of the cerebral cortex, and send signals back to both of these locations. They are involved in motor control. They are found lateral to the thalamus. The main components of the basal ganglia are the caudate nucleus, the putamen, the globus pallidus, the substantia nigra, the nucleus accumbens, and the subthalamic nucleus. The putamen and globus pallidus are also collectively known as the lentiform nucleus, because together they form a lens-shaped body. The putamen and caudate nucleus are also collectively called the corpus striatum after their striped appearance.[57][58]

Association areasEdit

The association areas are the parts of the cerebral cortex that do not belong to the primary regions. They function to produce a meaningful perceptual experience of the world, enable us to interact effectively, and support abstract thinking and language. The parietal, temporal, and occipital lobes - all located in the posterior part of the cortex - integrate sensory information and information stored in memory. The frontal lobe or prefrontal association complex is involved in planning actions and movement, as well as abstract thought. Globally, the association areas are organized as distributed networks.[59] Each network connects areas distributed across widely spaced regions of the cortex. Distinct networks are positioned adjacent to one another yielding a complex series of interwoven networks. The specific organization of the association networks is debated with evidence for interactions, hierarchical relationships, and competition between networks.[60] In humans, association networks are particularly important to language function. In the past it was theorized that language abilities are localized in the left hemisphere in areas 44/45, the Broca's area, for language expression and area 22, the Wernicke's area, for language reception. However, language is no longer limited to easily identifiable areas. More recent research suggests that the processes of language expression and reception occur in areas other than just those structures around the lateral sulcus, including the frontal lobe, basal ganglia, cerebellum, and pons.[61]

Clinical significanceEdit

There is marked cortical atrophy in Alzheimer's disease, associated with loss of gyri and sulci in the temporal lobe and parietal lobe, and parts of the frontal cortex and cingulate gyrus.

Neurodegenerative diseases such as Alzheimer's disease and Lafora disease, show as a marker, an atrophy of the grey matter of the cerebral cortex.[62]

There are many neurodevelopmental abnormalities that can lead to a wide variety of behavioral and cognitive deficits. There are several situations in development in which both intrinsic and extrinsic factors can highly influence the course of nervous system formation. One very prominent intrinsic factor (random gene mutation) has given rise to many different classes of neurodevelopmental disorders. For example, Fragile X-Syndrome is a neurodevelopmental disease characterized by poor eye contact with others, an extreme aversion to physical/social contact, and obsessive repetition in behavioral patterns.[63] This is an X-linked chromosomal disorder in which the FMR1 gene is found to have nearly 200 copies, instead of its intended 30. This causes the gene to become heavily methylated, which subsequently turns off expression of FMR1. Efficient functioning of this gene is known to play a role in localized protein synthesis at dendritic spines, which is essential for proper synaptogenesis and learning and memory function.[63]

Maternal alcohol consumption leads to death of neural crest cells which are the building blocks of certain neural tissues.

Another primary example of intrinsic neurodevelopmental deficits is Rett Syndrome, which is an X-linked single gene mutation characterized by a loss of speech and hand coordination, intellectual regression and progressive loss of motor control.[63] This disorder is thought to arise from a mutation in the MeCP2 gene, which encodes for a transcription factor associated with chromatin remodeling. Mutations in this gene have been linked to a decreased expression of the gene that codes for BDNF (brain-derived neurotrophic factor), which is a common gene used in neurodevelopment.[63]

A disorder of neuronal migration is lissencephaly a condition in which the cerebral surface is smooth without the convulutions of gyrification.

Apart from intrinsic gene mutation, there are many extrinsic (environmental) factors that can greatly influence the neurodevelopmental process. One of the most commonly studied factors is the effect of maternal alcohol consumption during gestation. Infants born with defects from this factor are said to have Fetal Alcohol Spectrum Disorder (FASD). FASD is used to describe a collection of developmental disorders associated with the consumption of alcohol whilst pregnant.[64] The spectrum includes individuals with both extreme and mild FASD which present with a variety of neurocognitive and neurobehavioral deficits. This includes deficits is sustained and focused attention, learning and memory problems, verbal processing problems, receptive language difficulties, hyperactivity, as well as a range of psychiatric impairments.[64] Apoptotic cell death caused by an excess of glutamate activity and GABA withdrawal is thought to play a role in the loss of neuronal fibers critical for normal brain development. In addition to neuronal death, there is evidence suggesting that an improper formation of interneuronal connections and cell adhesion molecule malformation are also associated with FASD. Improper neuronal migration and synaptogenesis have been shown to occur is several cases of FASD, which could explain the extreme deficits in learning and memory.[64]

Individuals with Fetal Alcohol Spectrum Disorder (FASD) exhibit a range of cognitive and behavioral deficits that relate heavily to neural pathologies associated with maternal alcohol consumption.

Other animalsEdit

The cerebral cortex is derived from the pallium, a layered structure found in the forebrain of all vertebrates. The basic form of the pallium is a cylindrical layer enclosing fluid-filled ventricles. Around the circumference of the cylinder are four zones, the dorsal pallium, medial pallium, ventral pallium, and lateral pallium, which are thought respectively to give rise to the neocortex, hippocampus, amygdala, and olfactory cortex.

Until recently no counterpart to the cerebral cortex had been recognized in invertebrates. However, a study published in the journal Cell in 2010, based on gene expression profiles, reported strong affinities between the cerebral cortex and the mushroom bodies of the ragworm Platynereis dumerilii.[65] Mushroom bodies are structures in the brains of many types of worms and arthropods that are known to play important roles in learning and memory; the genetic evidence indicates a common evolutionary origin, and therefore indicates that the origins of the earliest precursors of the cerebral cortex date back to the early Precambrian era.

Additional imagesEdit

See alsoEdit


  1. ^ a b c Saladin, Kenneth (2011). Human anatomy (3rd ed.). McGraw-Hill. pp. 416–422. ISBN 9780071222075.
  2. ^ Fernández, V; Llinares-Benadero, C; Borrell, V (17 May 2016). "Cerebral cortex expansion and folding: what have we learned?". The EMBO journal. 35 (10): 1021–44. doi:10.15252/embj.201593701. PMID 27056680.
  3. ^ a b c d Rakic, P (October 2009). "Evolution of the neocortex: a perspective from developmental biology". Nature Reviews Neuroscience. 10 (10): 724–35. doi:10.1038/nrn2719. PMC 2913577. PMID 19763105.
  4. ^ a b c Principles of neural science (4th ed.). McGraw-Hill, Health Professions Division. ISBN 0838577016.
  5. ^ Toro, Roberto; Perron, Michel; Pike, Bruce; Richer, Louis; Veillette, Suzanne; Pausova, Zdenka; Paus, Tomáš (2008-10-01). "Brain Size and Folding of the Human Cerebral Cortex". Cerebral Cortex. 18 (10): 2352–2357. doi:10.1093/cercor/bhm261. ISSN 1047-3211. PMID 18267953.
  6. ^ a b Nieuwenhuys R, Donkelaar HJ, Nicholson C (1998). The central nervous system of vertebrates, Volume 1. Springer. pp. 2011–2012. ISBN 978-3-540-56013-5.
  7. ^ Frithjof Kruggel; Martina K. Brückner; Thomas Arendt; Christopher J. Wiggins; D. Yves von Cramon (2003). "Analyzing the neocortical fine-structure". Medical Image Analysis. 7 (3): 251&ndash, 264. doi:10.1016/S1361-8415(03)00006-9.
  8. ^ Katherine L. Narr; Roger P. Woods; Paul M. Thompson; Philip Szeszko; Dilbert Robinson; Teodora Dimtcheva; Mala Gurbani; Arthur W. Toga; Robert M. Bilder (2007). "Relationships between IQ and Regional Cortical Grey Matter Thickness in Healthy Adults". Cerebral Cortex. 17 (9): 2163&ndash, 2171. doi:10.1093/cercor/bhl125. PMID 17118969.
  9. ^ Alexandre F.M. DaSilva; Cristina Granziera; Josh Snyder; Nouchine Hadjikhani (2007). "Thickening in the somatosensory cortex of patients with migraine". Neurology. 69 (21): 1990&ndash, 1995. doi:10.1212/01.wnl.0000291618.32247.2d. PMC 3757544. PMID 18025393.
  10. ^ Catharine Paddock (2007-11-20). "Migraine Sufferers Have Thicker Brain Cortex". Medical News Today. Archived from the original on 2008-05-11.
  11. ^ Datte R, Detre JA, et al. (Oct 2011). "Absence of changes in cortical thickness in patients with migraine". Cephalagia. 31 (14): 1452–8. doi:10.1177/0333102411421025. PMC 3512201. PMID 21911412.
  12. ^ Habib M (2000). "The neurological basis of developmental dyslexia: an overview and working hypothesis". Brain. 123 (12): 2373–99. doi:10.1093/brain/123.12.2373. PMID 11099442.
  13. ^ "Scientists identify a new kind of human brain cell". Allen Institute. 27 August 2018.
  14. ^ Shipp, Stewart (2007-06-17). "Structure and function of the cerebral cortex". Current Biology. 17 (12): R443–9. doi:10.1016/j.cub.2007.03.044. PMID 17580069. Archived from the original on 2010-10-02. Retrieved 2009-02-17.
  15. ^ Meyer, Gundela; Goffinet, André M.; Fairén, Alfonso (1999). "Feature Article: What is a Cajal–Retzius cell? A Reassessment of a Classical Cell Type Based on Recent Observations in the Developing Neocortex". Cerebral Cortex. 9 (8): 765–775. doi:10.1093/cercor/9.8.765. PMID 10600995. Archived from the original on 2015-02-21.
  16. ^ Judaš, Miloš; Pletikos, Mihovil (2010). "The discovery of the subpial granular layer in the human cerebral cortex". Translational Neuroscience. 1 (3): 255–260. doi:10.2478/v10134-010-0037-4. Archived from the original on 2016-03-12.
  17. ^ Gilbert CD, Sigman M (2007). "Brain states: top-down influences in sensory processing". Neuron. 54 (5): 677–96. doi:10.1016/j.neuron.2007.05.019. PMID 17553419.
  18. ^ Cauller L (1995). "Layer I of primary sensory neocortex: where top-down converges upon bottom-up". Behav Brain Res. 71 (1–2): 163–70. doi:10.1016/0166-4328(95)00032-1. PMID 8747184.
  19. ^ Rubio-Garrido P, Pérez-de-Manzo F, Porrero C, Galazo MJ, Clascá F (2009). "Thalamic input to distal apical dendrites in neocortical layer 1 is massive and highly convergent". Cereb Cortex. 19 (10): 2380–95. doi:10.1093/cercor/bhn259. PMID 19188274.
  20. ^ a b Jones EG (1998). "Viewpoint: the core and matrix of thalamic organization". Neuroscience. 85 (2): 331–45. doi:10.1016/S0306-4522(97)00581-2. PMID 9622234.
  21. ^ Creutzfeldt, O. 1995. Cortex Cerebri. Springer-Verlag.
  22. ^ a b Lam YW, Sherman SM (2010). "Functional Organization of the Somatosensory Cortical Layer 6 Feedback to the Thalamus". Cereb Cortex. 20 (1): 13–24. doi:10.1093/cercor/bhp077. PMC 2792186. PMID 19447861.
  23. ^ Mountcastle V (1997). "The columnar organization of the neocortex". Brain. 120 (4): 701–722. doi:10.1093/brain/120.4.701. PMID 9153131.
  24. ^ Hubel DH, Wiesel TN (October 1959). "Receptive fields of single neurones in the cat's striate cortex". The Journal of Physiology. 148 (3): 574–91. doi:10.1113/jphysiol.1959.sp006308. PMC 1363130. PMID 14403679.
  25. ^ S.M. Dombrowski, C.C. Hilgetag, and H. Barbas. Quantitative Architecture Distinguishes Prefrontal Cortical Systems in the Rhesus Monkey Archived 2008-08-29 at the Wayback Machine..Cereb. Cortex 11: 975–988. "...they either lack (agranular) or have only a rudimentary granular layer IV (dysgranular)."
  26. ^ Sun W, Dan Y (2009). "Layer-specific network oscillation and spatiotemporal receptive field in the visual cortex". Proc Natl Acad Sci U S A. 106 (42): 17986–17991. Bibcode:2009PNAS..10617986S. doi:10.1073/pnas.0903962106. PMC 2764922. PMID 19805197.
  27. ^ Principles of Anatomy and Physiology 12th Edition - Tortora, Page 519-fig. (14.15)
  28. ^ Pletikos, Mihovil; Sousa, Andre MM; et al. (22 January 2014). "Temporal Specification and Bilaterality of Human Neocortical Topographic Gene Expression". Neuron. 81 (2): 321–332. doi:10.1016/j.neuron.2013.11.018. PMC 3931000. PMID 24373884.
  29. ^ Warren N, Caric D, Pratt T, Clausen JA, Asavaritikrai P, Mason JO, Hill RE, Price DJ (1999). "The transcription factor, Pax6, is required for cell proliferation and differentiation in the developing cerebral cortex". Cerebral Cortex. 9 (6): 627–35. doi:10.1093/cercor/9.6.627. PMID 10498281.
  30. ^ Larsen, W J. Human Embryology 3rd edition 2001. pp 421-422 ISBN 0-443-06583-7
  31. ^ Stephen C. Noctor; Alexander C. Flint; Tamily A. Weissman; Ryan S. Dammerman & Arnold R. Kriegstein (2001). "Neurons derived from radial glial cells establish radial units in neocortex". Nature. 409 (6821): 714&ndash, 720. doi:10.1038/35055553. PMID 11217860. Archived from the original on 2007-09-29.
  32. ^ Rakic, P (October 2009). "Evolution of the neocortex: a perspective from developmental biology". Nature Reviews Neuroscience. 10 (10): 724–35. doi:10.1038/nrn2719. PMC 2913577. PMID 19763105.
  33. ^ Rakic, P (November 1972). "Extrinsic cytological determinants of basket and stellate cell dendritic pattern in the cerebellar molecular layer". The Journal of Comparative Neurology. 146 (3): 335–54. doi:10.1002/cne.901460304. PMID 4628749.
  34. ^ Calegari, F; Haubensack W; Haffner C; Huttner WB (2005). "Selective lengthening of the cell cycle in the neurogenic subpopulation of neural progenitor cells during mouse brain development". The Journal of Neuroscience. 25 (28): 6533–8. doi:10.1523/jneurosci.0778-05.2005. PMID 16014714.
  35. ^ P. Rakic (1988). "Specification of cerebral cortical areas". Science. 241 (4862): 170&ndash, 176. Bibcode:1988Sci...241..170R. doi:10.1126/science.3291116. PMID 3291116. Archived from the original on 2007-09-30.
  36. ^ Hu, X.L.; Wang, Y.; Shen, Q. (2012). "Epigenetic control on cell fate choice in neural stem cells". Protein & Cell. 3 (4): 278–290. doi:10.1007/s13238-012-2916-6. PMC 4729703. PMID 22549586.
  37. ^ Kostović, Ivica (1990). "Developmental history of the transient subplate zone in the visual and somatosensory cortex of the macaque monkey and human brain". Journal of Comparative Neurology. 297 (3): 441–470. doi:10.1002/cne.902970309.
  38. ^ Rakic, P (1 February 1974). "Neurons in rhesus monkey visual cortex: systematic relation between time of origin and eventual disposition". Science. 183 (4123): 425–7. Bibcode:1974Sci...183..425R. doi:10.1126/science.183.4123.425. PMID 4203022.
  39. ^ Zecevic N, Rakic P (2001). "Development of layer I neurons in the primate cerebral cortex". The Journal of Neuroscience. 21 (15): 5607–19. PMID 11466432. Archived from the original on 2009-12-13.
  40. ^ Rakic, P (8 July 1988). "Specification of cerebral cortical areas". Science. 241 (4862): 170–6. Bibcode:1988Sci...241..170R. doi:10.1126/science.3291116. PMID 3291116.
  41. ^ Fukuchi-Shimogori, T; Grove, EA (2 November 2001). "Neocortex patterning by the secreted signaling molecule FGF8". Science. 294 (5544): 1071–4. Bibcode:2001Sci...294.1071F. doi:10.1126/science.1064252. PMID 11567107.
  42. ^ Garel, S; Huffman, KJ; Rubenstein, JL (May 2003). "Molecular regionalization of the neocortex is disrupted in Fgf8 hypomorphic mutants". Development. 130 (9): 1903–14. doi:10.1242/dev.00416. PMID 12642494.
  43. ^ Bishop, KM; Goudreau, G; O'Leary, DD (14 April 2000). "Regulation of area identity in the mammalian neocortex by Emx2 and Pax6". Science. 288 (5464): 344–9. Bibcode:2000Sci...288..344B. doi:10.1126/science.288.5464.344. PMID 10764649.
  44. ^ a b c Sanes, Dan H.; Reh, Thomas A.; Harris, William A. (2012). Development of the Nervous System. Elsevier Inc. ISBN 978-0-12-374539-2.
  45. ^ Rash, BG; Lim, HD; Breunig, JJ; Vaccarino, FM (26 October 2011). "FGF signaling expands embryonic cortical surface area by regulating Notch-dependent neurogenesis". The Journal of Neuroscience. 31 (43): 15604–17. doi:10.1523/jneurosci.4439-11.2011. PMC 3235689. PMID 22031906.
  46. ^ Rajagopalan, V; Scott, J; Habas, PA; Kim, K; Corbett-Detig, J; Rousseau, F; Barkovich, AJ; Glenn, OA; Studholme, C (23 February 2011). "Local tissue growth patterns underlying normal fetal human brain gyrification quantified in utero". The Journal of Neuroscience. 31 (8): 2878–87. doi:10.1523/jneurosci.5458-10.2011. PMC 3093305. PMID 21414909.
  47. ^ Lui, Jan H.; Hansen, David V.; Kriegstein, Arnold R. (2011-07-08). "Development and evolution of the human neocortex". Cell. 146 (1): 18–36. doi:10.1016/j.cell.2011.06.030. ISSN 1097-4172. PMC 3610574. PMID 21729779.
  48. ^ Stahl, Ronny; Walcher, Tessa; De Juan Romero, Camino; Pilz, Gregor Alexander; Cappello, Silvia; Irmler, Martin; Sanz-Aquela, José Miguel; Beckers, Johannes; Blum, Robert (2013-04-25). "Trnp1 regulates expansion and folding of the mammalian cerebral cortex by control of radial glial fate". Cell. 153 (3): 535–549. doi:10.1016/j.cell.2013.03.027. ISSN 1097-4172. PMID 23622239.
  49. ^ Wang, Lei; Hou, Shirui; Han, Young-Goo (2016-05-23). "Hedgehog signaling promotes basal progenitor expansion and the growth and folding of the neocortex". Nature Neuroscience. 19 (7): 888–96. doi:10.1038/nn.4307. ISSN 1546-1726. PMC 4925239. PMID 27214567.
  50. ^ Rash, Brian G.; Tomasi, Simone; Lim, H. David; Suh, Carol Y.; Vaccarino, Flora M. (2013-06-26). "Cortical gyrification induced by fibroblast growth factor 2 in the mouse brain". The Journal of Neuroscience. 33 (26): 10802–10814. doi:10.1523/JNEUROSCI.3621-12.2013. ISSN 1529-2401. PMC 3693057. PMID 23804101.
  51. ^ Sur, Mriganka; Leamey, Catherine A. (2001). "Development and Plasticity of Cortical Areas and Networks". Nature Reviews Neuroscience. 2 (4): 251–262. doi:10.1038/35067562.
  52. ^ Rakic, P (8 July 1988). "Specification of cerebral cortical areas". Science. 241 (4862): 170–6. Bibcode:1988Sci...241..170R. doi:10.1126/science.3291116. PMID 3291116.
  53. ^ Fukuchi-Shimogori, T; Grove, EA (2 November 2001). "Neocortex patterning by the secreted signaling molecule FGF8". Science. 294 (5544): 1071–4. Bibcode:2001Sci...294.1071F. doi:10.1126/science.1064252. PMID 11567107.
  54. ^ Bishop, KM; Goudreau, G; O'Leary, DD (14 April 2000). "Regulation of area identity in the mammalian neocortex by Emx2 and Pax6". Science. 288 (5464): 344–9. Bibcode:2000Sci...288..344B. doi:10.1126/science.288.5464.344. PMID 10764649.
  55. ^ Grove, EA; Fukuchi-Shimogori, T (2003). "Generating the cerebral cortical area map". Annual Review of Neuroscience. 26: 355–80. doi:10.1146/annurev.neuro.26.041002.131137. PMID 14527269.
  56. ^ Braitenberg, V and Schüz, A 1998. "Cortex: Statistics and Geometry of Neuronal Connectivity. Second thoroughly revised edition" New York: Springer-Verlag
  57. ^ Saladin, Kenneth. Anatomy and Physiology: The Unity of Form and Function, 5th Ed. New York: McGraw-Hill Companies Inc., 2010. Print.
  58. ^ Dorland’s Medical Dictionary for Health Consumers, 2008.
  59. ^ Yeo BT, Krienen FM, Sepulcre J, Sabuncu MR, Lashkari D, Hollinshead M, Roffman JL, Smoller JW, Zöllei L, Polimeni JR, Fischl B, Liu H, Buckner RL (2011). "The organization of the human cerebral cortex estimated by intrinsic functional connectivity". Journal of Neurophysiology. 106 (3): 1125–1165. doi:10.1152/jn.00338.2011. PMC 3174820. PMID 21653723.
  60. ^ Rupesh Kumar Srivastava; Jürgen Schmidhuber (2014). "Understanding Locally Competitive Networks". arXiv:1410.1165 [cs.NE].
  61. ^ Cathy J. Price (2000). "The anatomy of language: contributions from functional neuroimaging". Journal of Anatomy. 197 (3): 335–359. doi:10.1046/j.1469-7580.2000.19730335.x. PMC 1468137.
  62. ^ Ortolano S, Vieitez I, et al. (2014). "Loss of cortical neurons underlies the neuropathology of Lafora disease". Mol Brain. 7: 7. doi:10.1186/1756-6606-7-7. PMC 3917365. PMID 24472629.
  63. ^ a b c d Kandel, Eric R.; Schwartz, James H.; Jessell, Thomas M.; Siegelbaum, Steven A.; Hudspeth, A.J. (2013). Principles of Neural Science. United States of America: McGraw-Hill. p. 1435. ISBN 978-0-07-139011-8.
  64. ^ a b c Mukherjee, Raja A.S.; Hollins, Sheila (2006). "Fetal Alcohol Spectrum Disorder: An Overview". Journal of the Royal Society of Medicine. 99 (6): 298–302. doi:10.1258/jrsm.99.6.298. PMC 1472723. PMID 16738372.
  65. ^ Tomer, R; Denes, AS; Tessmar-Raible, K; Arendt, D; Tomer R; Denes AS; Tessmar-Raible K; Arendt D (2010). "Profiling by image registration reveals common origin of annelid mushroom bodies and vertebrate pallium". Cell. 142 (5): 800–809. doi:10.1016/j.cell.2010.07.043. PMID 20813265.

External linksEdit