Document Detail


Non-lethal active caspase-3 expression in Bergmann glia of postnatal rat cerebellum.
MedLine Citation:
PMID:  16226814     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Caspase-3, an apoptotic executor, has been shown in recent years to mediate non-lethal events like cellular proliferation and differentiation, primarily in studies related to non-neural tissue. In central nervous system development, the role of active caspase-3 is still unclear. We provide the first evidence for a potential new role of active (cleaved) caspase-3 in promoting differentiation of Bergmann glia. This study was predicated on the hypothesis that active caspase-3 is important for the differentiation of glia. We addressed the hypothesis through the following specific aims: (1) to establish the expression of active caspase-3 in glia; (2) to determine the developmental phenotype of the active caspase-3-expressing glia; and (3) to confirm that active caspase-3 expression is not mediating an apoptotic event. Through a temporal investigation from postnatal day 8 to 21, we observed that Bergmann glia express active caspase-3 without compromising their survival. Potential apoptotic fate of active caspase-3-positive Bergmann glia were ruled out based on immunohistochemical exclusion of phosphatidylserine exposure (Annexin V), DNA fragmentation (TUNEL), and DNA compaction (TOPRO-3). More than 90% of the active caspase-3-positive cells lacked colabeling for one of the apoptotic markers. Correlative studies using a proliferation marker Ki67 and a differentiation marker brain lipid-binding protein suggest that the expression of active caspase-3 was mostly associated with differentiating rather than proliferating Bergmann glia at all ages. Thus, this study supports the hypothesis that active caspase-3 may be regulating both differentiation of Bergmann glia by allowing the cells to exit the cell cycle and their morphogenesis.
Authors:
Sowmini Oomman; Howard Strahlendorf; VelvetLee Finckbone; Jean Strahlendorf
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't     Date:  2005-10-14
Journal Detail:
Title:  Brain research. Developmental brain research     Volume:  160     ISSN:  0165-3806     ISO Abbreviation:  Brain Res. Dev. Brain Res.     Publication Date:  2005 Dec 
Date Detail:
Created Date:  2005-12-02     Completed Date:  2006-02-07     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  8908639     Medline TA:  Brain Res Dev Brain Res     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  130-45     Citation Subset:  IM    
Affiliation:
Department of Physiology, Texas Tech University Health Sciences Center, Room 5A163, Lubbock, TX 79430, USA.
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MeSH Terms
Descriptor/Qualifier:
Age Factors
Animals
Animals, Newborn
Annexin A5 / metabolism
Apoptosis / drug effects,  physiology
Calcium-Binding Protein, Vitamin D-Dependent / metabolism
Caspase 3
Caspases / metabolism*
Cell Count / methods
Cerebellum / cytology*,  growth & development,  metabolism
Fatty Acid-Binding Proteins / metabolism
Gene Expression Regulation, Developmental / physiology*
Immunohistochemistry / methods
In Situ Nick-End Labeling / methods
Ki-67 Antigen / metabolism
Nerve Growth Factors / metabolism
Nerve Tissue Proteins / metabolism
Neuroglia / enzymology*
Phosphopyruvate Hydratase / metabolism
Quinolines / diagnostic use
Rats
Rats, Sprague-Dawley
S100 Proteins / metabolism
Statistics, Nonparametric
Staurosporine / adverse effects
Tubulin / metabolism
Chemical
Reg. No./Substance:
0/Annexin A5; 0/Calcium-Binding Protein, Vitamin D-Dependent; 0/Fabp7 protein, rat; 0/Fatty Acid-Binding Proteins; 0/Ki-67 Antigen; 0/Nerve Growth Factors; 0/Nerve Tissue Proteins; 0/Quinolines; 0/S-100 calcium-binding protein beta subunit; 0/S100 Proteins; 0/Tubulin; 0/calbindin; 62996-74-1/Staurosporine; EC 3.4.22.-/Casp3 protein, rat; EC 3.4.22.-/Caspase 3; EC 3.4.22.-/Caspases; EC 4.2.1.11/Phosphopyruvate Hydratase

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


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