Document Detail


Upregulation of Beclin 1 in the ischemic penumbra.
MedLine Citation:
PMID:  18075295     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Here we discuss the probable role of autophagy in cerebral ischemia based on our own recent data and the literature. We examined the protein level of Beclin 1 (Bcl-2 interacting protein) and microtubule-associated protein 1 light chain 3 (LC3) which were previously found to promote autophagy. We found a dramatic elevation in Beclin 1 levels and LC3 in the penumbra of rats challenged by cerebral ischemia. We found also that a subpopulation of Beclin 1-upregulating cells is also expressing the active form of caspase-3, and that all Beclin 1 upregulating cells display dense staining of LC3. Neuronal cells that overexpress Beclin 1 may exhibit damaged DNA but without changes in nuclear morphology, which indicates that not all the Beclin 1-upregulating cells are predestined to die. We conclude that the cell death in the penumbra bears a resemblance not only to necrosis, apoptosis, or a compromise between the two, but exhibits also biochemical and morphological characteristics of autophagic cell death. The question that constantly arises, however, is whether autophagic activity in damaged cells is the cause of death or is actually an attempt to prevent it as a part of an endogenous neuroprotective response.
Authors:
Abdelhaq Rami
Related Documents :
18221365 - Calcineurin is involved in the early activation of nmda-mediated cell death in mutant h...
9111315 - Human bak induces cell death in schizosaccharomyces pombe with morphological changes si...
16185655 - Nano neodymium oxide induces massive vacuolization and autophagic cell death in non-sma...
20722725 - On the paradigm of altruistic suicide in the unicellular world.
7585945 - Signals for death and survival: a two-step mechanism for cavitation in the vertebrate e...
22019895 - The cytotoxic effect of palytoxin on caco-2 cells hinders their use for in vitro absorp...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review     Date:  2007-11-27
Journal Detail:
Title:  Autophagy     Volume:  4     ISSN:  1554-8635     ISO Abbreviation:  Autophagy     Publication Date:  2008 Feb 
Date Detail:
Created Date:  2008-01-21     Completed Date:  2008-03-19     Revised Date:  2011-06-30    
Medline Journal Info:
Nlm Unique ID:  101265188     Medline TA:  Autophagy     Country:  United States    
Other Details:
Languages:  eng     Pagination:  227-9     Citation Subset:  IM    
Affiliation:
Institute of Cellular and Molecular Anatomy (Anatomie III), Dr. Senckenbergische Anatomie, Klinikum der Johann Wolfgang von Goethe-Universität, Franfurt/Main, Germany. Rami@em.uni-frankfurt.de
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Apoptosis Regulatory Proteins / genetics*,  metabolism
Autophagy / genetics
Biological Markers / metabolism
Brain Ischemia / genetics*,  metabolism
Cell Death
Cerebral Cortex / metabolism*
Microtubule-Associated Proteins / metabolism
Models, Biological
Protein Transport
Rats
Up-Regulation*
Chemical
Reg. No./Substance:
0/Apoptosis Regulatory Proteins; 0/Biological Markers; 0/LC3 protein, rat; 0/Microtubule-Associated Proteins; 0/beclin 1 protein, rat

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


Previous Document:  Somatostatin receptor scintigraphy in thoracic diseases.
Next Document:  Controlled internalization of Her-2/ neu receptors by cross-linking for targeted delivery.