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[3] [4] [5] Once there, the electrical signal provokes the release of chemical neurotransmitters across the synapse, which bind to receptors on the post-synaptic cell (e.g. another neuron, myocyte or secretory cell). Myelin is made by glial cells, which are non-neuronal cells that provide nutritional and homeostatic support to the axons
Myelin is formed by oligodendrocytes in the central nervous system and Schwann cells in the peripheral nervous system.Therefore, the first stage of myelinogenesis is often defined as the differentiation of oligodendrocyte progenitor cells (OPCs) or Schwann cell progenitors into their mature counterparts, [4] followed by myelin formation around axons.
Schwann cells are a variety of glial cells that keep peripheral nerve fibres (both myelinated and unmyelinated) alive. In myelinated axons, Schwann cells form the myelin sheath. The sheath is not continuous. Individual myelinating Schwann cells cover about 1 mm of an axon [3] – equating to about 1000 Schwann cells along a 1-m length of the axon.
This narrow zone is identified visually where there is a transition regarding myelin production. It is named after Emil Redlich and Heinrich Obersteiner. [1] As the Redlich–Obersteiner's zone separates the CNS and PNS, there is a transition from Schwann cell myelin to oligodendrocyte myelin. In cranial nerves this is often the place of neuro ...
Oligodendrocytes are a type of glial cell, non-neuronal cells in the central nervous system.They arise during development from oligodendrocyte precursor cells (OPCs), [8] which can be identified by their expression of a number of antigens, including the ganglioside GD3, [9] [10] [11] the NG2 chondroitin sulfate proteoglycan, and the platelet-derived growth factor-alpha receptor subunit (PDGF ...
Oligodendrocyte progenitor cells (OPCs), also known as oligodendrocyte precursor cells, NG2-glia, O2A cells, or polydendrocytes, are a subtype of glia in the central nervous system named for their essential role as precursors to oligodendrocytes and myelin. [1] They are typically identified in the human by co-expression of PDGFRA and CSPG4.
On the other hand, in the PNS, the basal lamina that surrounds the Schwann cells is continuous across the node. A study suggests that in the CNS, nerve cells individually alter the size of the nodes to tune conduction speeds, leading node length to vary much more across different axons than within one. [7]
Neuroregeneration differs between the peripheral nervous system (PNS) and the central nervous system (CNS) by the functional mechanisms involved, especially in the extent and speed of repair. When an axon is damaged, the distal segment undergoes Wallerian degeneration , losing its myelin sheath.