Document Detail


Schwann cell proliferation following lysolecithin-induced demyelination.
MedLine Citation:
PMID:  2391539     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Schwann cell division, meticulously regulated throughout development, occurs at an extremely low level in normal adult nerves. Loss of the myelin sheath in disease results in active proliferation of Schwann cells. The dividing cells are usually thought to be the Schwann cells of the demylinated fibres and their daughters. In this study we asked if other populations of Schwann cells might also divide following focal monophasic demyelination, and if the proliferating Schwann cells would be found only in the foci of demyelination. [3H]thymidine incorporation was examined by autoradiography at intervals after topical application of lysolecithin (lysophosphatidyl choline) to rat sciatic nerves. The postlabelling intervals were set to identify premitotic cells, cells shortly after mitosis (perimitotic cells) and postmitotic cells, as well as to provide cumulative labelling over 3 days. The affected nerves had three distinct zones. The first was a zone of nearly complete demyelination immediately beneath the perineurium. The subjacent zone was normal morphologically except for numerous supernumerary Schwann cells, displacement of some Schwann cell perikarya, ultrastructural changes in a few myelinated fibres, and rare demyelinated and remyelinated fibres. The third zone, beneath the first two, was normal. In the focus of demyelination there were large numbers of Schwann cells in S phase on days 4 and 6. These cells included premyelinating Schwann cells that were contacting or ensheathing demyelinated axons or collateral axonal sprouts. The subjacent region also contained dividing Schwann cells, most of which were Schwann cells of unmyelinated Remak fibres. In addition, occasional Schwann cells of thickly myelinated fibres (fibres that had not previously undergone demyelination) were labelled by the premitotic schedule; most of these fibres had morphological abnormalities in the Schwann cell perikaryon or myelin sheath. In many, the perikaryon of the Schwann cell was beginning to separate from the rest of the Schwann cell cytoplasm and the myelin sheath. These changes suggested that these fibres were destined to undergo subsequent demyelination, a hypothesis supported by the absence of any normal myelinated fibres with labelled Schwann cell nuclei in nerves removed 1 week after labelling. Thus, this model provided no evidence for division by Schwann cells that continued to maintain myelin sheaths. Taken together, these results suggest that there is a 'surround' of Schwann cell proliferation around foci of demyelination; in this surround multiple populations of Schwann cells are recruited to proliferate, including Schwann cells of intact unmyelinated fibres. Structurally normal unmyelinated fibres appear to provide an unexpected source of new Schwann cells in nerve disease.
Authors:
J W Griffin; E A Stocks; K Fahnestock; A Van Praagh; B D Trapp
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Journal of neurocytology     Volume:  19     ISSN:  0300-4864     ISO Abbreviation:  J. Neurocytol.     Publication Date:  1990 Jun 
Date Detail:
Created Date:  1990-10-04     Completed Date:  1990-10-04     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  0364620     Medline TA:  J Neurocytol     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  367-84     Citation Subset:  IM    
Affiliation:
Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
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MeSH Terms
Descriptor/Qualifier:
Administration, Topical
Animals
Autoradiography
Cell Division
Demyelinating Diseases / chemically induced,  pathology*
Lysophosphatidylcholines / administration & dosage
Microinjections
Nerve Fibers, Myelinated / pathology
Rats
Rats, Inbred Strains
Schwann Cells / pathology*
Thymidine / pharmacology
Tritium / diagnostic use
Grant Support
ID/Acronym/Agency:
P01-22849//PHS HHS; R01-14784//PHS HHS
Chemical
Reg. No./Substance:
0/Lysophosphatidylcholines; 10028-17-8/Tritium; 50-89-5/Thymidine

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