Document Detail


Cells expressing the NG2 antigen contact nodes of Ranvier in adult CNS white matter.
MedLine Citation:
PMID:  10088675     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The NG2 antibody, which recognises an integral membrane chondroitin sulphate, labels a significant population of cells in adult CNS white matter tracts of the rat optic nerve and anterior medullary velum (AMV). Adult NG2+ cells are highly complex with multiple branching processes and we show by EM immunocytochemistry that they extend perinodal processes, which contact nodes of Ranvier. NG2+ cells do not react to conventional immunohistochemical markers for adult glia and so we reservedly term them NG2P cells. In vitro, NG2 labels oligodendrocyte-type-2 astrocyte (O-2A) progenitors that can give rise to oligodendrocytes or type-2 astrocytes, depending on the culture medium. Thus, it is possible that NG2P cells may be derived from the same stem cells as oligodendrocytes. Interestingly, NG2+ cells identified previously in adult CNS displayed phenotypic characteristics of O-2Aadult progenitors and it is possible that, like them, NG2P cells might retain the capacity of generating oligodendrocytes in the adult CNS. This may be an important role of NG2P cells in demyelinating diseases such as multiple sclerosis. It is significant therefore that the perinodal processes of NG2P cells contact the only sites of exposed axolemma in myelinated axons, so that NG2P cells are ideally situated to detect and respond to changes in axonal function during demyelination. A further implication of our finding is that NG2P cells may perform functions at nodes of Ranvier previously attributed to perinodal astrocytes, including the clustering and maintenance of sodium channels in the axon membrane at nodes, during development and following demyelination.
Authors:
A M Butt; A Duncan; M F Hornby; S L Kirvell; A Hunter; J M Levine; M Berry
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Glia     Volume:  26     ISSN:  0894-1491     ISO Abbreviation:  Glia     Publication Date:  1999 Mar 
Date Detail:
Created Date:  1999-05-13     Completed Date:  1999-05-13     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  8806785     Medline TA:  Glia     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  84-91     Citation Subset:  IM    
Affiliation:
Division of Physiology, Guy's, King's and St. Thomas' School of Biomedical Sciences, King's College London, United Kingdom. a.butt@umds.ac.uk
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MeSH Terms
Descriptor/Qualifier:
Animals
Antigens / immunology,  physiology*
Astrocytes / cytology,  physiology,  ultrastructure
Axons / physiology
Cerebral Ventricles / cytology,  physiology*,  ultrastructure
Female
Intercellular Junctions / physiology*,  ultrastructure
Microscopy, Immunoelectron
Neuroglia / cytology,  physiology*,  ultrastructure
Oligodendroglia / cytology,  physiology,  ultrastructure
Optic Nerve / cytology,  physiology*,  ultrastructure
Proteoglycans / immunology,  physiology*
Ranvier's Nodes / physiology*,  ultrastructure
Rats
Rats, Wistar
Sodium Channels / physiology
Stem Cells / cytology,  physiology
Chemical
Reg. No./Substance:
0/Antigens; 0/Proteoglycans; 0/Sodium Channels; 0/chondroitin sulfate proteoglycan 4

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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