Literature DB >> 8613761

Connexin32 is a myelin-related protein in the PNS and CNS.

S S Scherer1, S M Deschênes, Y T Xu, J B Grinspan, K H Fischbeck, D L Paul.   

Abstract

We have examined the expression of a gap junction protein, connexin32 (Cx32), in Schwann cells and oligodendrocytes. In peripheral nerve, Cx32 is found in the paranodal myelin loops and Schmidt-Lanterman incisures of myelinating Schwann cells, and the levels of Cx32 protein and mRNA change in parallel with those of other myelin-related genes during development, Wallerian degeneration, and axonal regeneration. In the central nervous system, Cx32 is found in oligodendrocytes and their processes, but not in compact myelin, and the levels of Cx32 protein and mRNA increase during development in parallel with those of the other myelin genes. Thus, Cx32 is expressed as part of the myelinating phenotype of both Schwann cells and oligodendrocytes, indicating that this gap junction protein plays in important role in the biology of myelin-forming cells.

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Year:  1995        PMID: 8613761      PMCID: PMC6577923     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  95 in total

1.  Astrocyte and oligodendrocyte connexins of the glial syncytium in relation to astrocyte anatomical domains and spatial buffering.

Authors:  James I Nagy; John E Rash
Journal:  Cell Commun Adhes       Date:  2003 Jul-Dec

2.  The role of gap junctions in Charcot-Marie-Tooth disease.

Authors:  Kleopas A Kleopa
Journal:  J Neurosci       Date:  2011-12-07       Impact factor: 6.167

3.  Inflammatory demyelinating CNS disorder in a case of X-linked Charcot-Marie-Tooth disease: positive response to natalizumab.

Authors:  Jochen H Weishaupt; Claudia Ganser; Mathias Bähr
Journal:  J Neurol       Date:  2012-03-13       Impact factor: 4.849

4.  Morphological and electrical properties of oligodendrocytes in the white matter of the corpus callosum and cerebellum.

Authors:  Yamina Bakiri; Ragnhildur Káradóttir; Lee Cossell; David Attwell
Journal:  J Physiol       Date:  2010-11-22       Impact factor: 5.182

5.  Axonal pathology precedes demyelination in a mouse model of X-linked demyelinating/type I Charcot-Marie Tooth neuropathy.

Authors:  Natalie Vavlitou; Irene Sargiannidou; Kyriaki Markoullis; Kyriacos Kyriacou; Steven S Scherer; Kleopas A Kleopa
Journal:  J Neuropathol Exp Neurol       Date:  2010-09       Impact factor: 3.685

6.  HNMP-1: a novel hematopoietic and neural membrane protein differentially regulated in neural development and injury.

Authors:  L M Bolin; T McNeil; L A Lucian; B DeVaux; K Franz-Bacon; D M Gorman; S Zurawski; R Murray; T K McClanahan
Journal:  J Neurosci       Date:  1997-07-15       Impact factor: 6.167

7.  Functional alterations in gap junction channels formed by mutant forms of connexin 32: evidence for loss of function as a pathogenic mechanism in the X-linked form of Charcot-Marie-Tooth disease.

Authors:  C K Abrams; M M Freidin; V K Verselis; M V Bennett; T A Bargiello
Journal:  Brain Res       Date:  2001-05-04       Impact factor: 3.252

8.  Tricellulin is expressed in autotypic tight junctions of peripheral myelinating Schwann cells.

Authors:  Shin Kikuchi; Takafumi Ninomiya; Haruyuki Tatsumi; Norimasa Sawada; Takashi Kojima
Journal:  J Histochem Cytochem       Date:  2010-12       Impact factor: 2.479

Review 9.  Life cycle of connexins in health and disease.

Authors:  Dale W Laird
Journal:  Biochem J       Date:  2006-03-15       Impact factor: 3.857

10.  A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon.

Authors:  Zongming Pan; Tingching Kao; Zsolt Horvath; Julia Lemos; Jai-Yoon Sul; Stephen D Cranstoun; Vann Bennett; Steven S Scherer; Edward C Cooper
Journal:  J Neurosci       Date:  2006-03-08       Impact factor: 6.167

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