The
mammalian cerebral cortex, the
grey matter encapsulating the
white matter, is composed of
layers. The
human cortex is between 2 and 3 mm thick. The number of layers is the same in most mammals, but varies throughout the cortex.
6 layers can be recognized in the neocortex, although many regions lack one or more layers. For example, fewer layers are present in the
archipallium and the
paleopallium. The 6 layer model of the
cerebral cortex defines layers by frequency of cell type. Layer 1 (L1), called the molecular layer, lies in the most superior in the cortex and mainly contains
dendrites,
axons, and axon terminals. L2 and L3 lie just underneath L1 and both layers contain
pyramidal cells, with the size of these cells increasing in the deepest part of L3. L2 and L3 pyramidal axons project to both local and non-local cortical areas. L4, termed the
granular layer, is generally responsible for receiving signals from the
thalamus, therefore controlling the sensory input of many different cortical areas. L4 is composed of mostly small spherical neurons. L5 is the most inferior layer composed of pyramidal cells. The large pyramidal cells in L5 are responsible for large outputs to subcortical and other cortical areas. L6 is
multiform and generally consists of axon projections between structures. Cortical columns are viewed as vertical projections of cells in these layers.
Columnar functional organization The columnar functional organization, as originally framed by
Vernon Mountcastle, Various estimates suggest there are 50 to 100
cortical minicolumns in a hypercolumn, each comprising around 80 neurons. Their role is best understood as 'functional units of information processing.' An important distinction is that the columnar organization is functional by definition, and reflects the local connectivity of the cerebral cortex. Connections "up" and "down" within the thickness of the cortex are much denser than connections that spread from side to side. ==Hubel and Wiesel studies==