Document Detail


Microglial turnover in the injured CNS: activated microglia undergo delayed DNA fragmentation following peripheral nerve injury.
MedLine Citation:
PMID:  7666057     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Microglial proliferation and activation are common events in the injured CNS. The mechanisms, however, by which activated microglia are eliminated following a pathological stimulus are still poorly understood. The present study has therefore examined microglial proliferation by 3H-thymidine autoradiography and programmed cell death by terminal transferase-mediated nick end labeling (TUNEL) and in situ end labeling (ISEL) of nuclear DNA fragments in two models of peripheral nerve injury, i.e. sciatic and hypoglossal nerve transection in the rat. In these models, microglial activation and proliferation occur in CNS projection areas, i.e. in the ventral and dorsal gray matter of lumbar spinal cord and in the nucleus gracilis after sciatic nerve transection as well as in the axotomized hypoglossal nucleus. At these sites, microglial proliferation had a relatively sharp peak between days 2 and 3 post-lesion and then rapidly declined. DNA fragmentation was detected in lectin (GSI-B4)-positive microglia from day 6 after axotomy onward, reached an apparent peak at day 21 and was downregulated by day 60, i.e. the latest time point investigated. However, the expression of bcl-2 and c-myc, i.e. genes potentially controlling programmed cell death, was found to be unchanged during this period. Programmed cell death thus appears to be one mechanism by which activated microglia are gradually eliminated following CNS injury and steady state of microglial cell numbers is achieved in vivo. Expression of microglial growth factors may be instrumental in controlling these processes.
Authors:
J Gehrmann; R B Banati
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of neuropathology and experimental neurology     Volume:  54     ISSN:  0022-3069     ISO Abbreviation:  J. Neuropathol. Exp. Neurol.     Publication Date:  1995 Sep 
Date Detail:
Created Date:  1995-10-06     Completed Date:  1995-10-06     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  2985192R     Medline TA:  J Neuropathol Exp Neurol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  680-8     Citation Subset:  IM    
Affiliation:
Department of Pathology, University Hospital Zürich, Switzerland.
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MeSH Terms
Descriptor/Qualifier:
Animals
Apoptosis
Brain / cytology,  pathology*
Cell Nucleus / metabolism,  pathology
DNA / analysis,  metabolism*
Hypoglossal Nerve / injuries*,  pathology*,  physiology
Male
Microglia / cytology,  pathology*
Nerve Regeneration
Periaqueductal Gray / cytology,  pathology
Rats
Rats, Wistar
Reference Values
Sciatic Nerve / injuries*,  physiology
Spinal Cord / cytology,  pathology*
Time Factors
Chemical
Reg. No./Substance:
9007-49-2/DNA

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


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