Document Detail


Re-entry into the cell cycle: a mechanism for neurodegeneration in Alzheimer disease.
MedLine Citation:
PMID:  10459833     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Several recent findings demonstrated increased expression of cell cycle-related proteins in the degenerating neurons found in Alzheimer disease. We hypothesize that this apparent attempt to re-enter the cell cycle is a neuronal response to external growth stimuli that leads to an abortive re-entry into the cell cycle. However, since neurons of adults apparently lack the capacity both to divide in vivo and in vitro, it is possible that they lack the components necessary to complete the cell division process. Nonetheless, the importance of these findings is that they provide an explanation for the increased phosphorylation of cytoskeletal proteins such as tau and neurofilaments that represent the most striking intracellular changes in the disease. Further, it is our contention that inappropriate reentry into the cell cycle and interrupted mitotic processes are significant factors not only in the cytoskeletal pathology but also in the neuronal degeneration that characterizes the pathology of Alzheimer disease.
Authors:
A McShea; A F Wahl; M A Smith
Related Documents :
19818353 - Positive-feedback loops in cell cycle progression.
20093253 - Cell cycle-dependent expression of kv3.4 channels modulates proliferation of human uter...
4066773 - On the role of 17 alpha-estradiol and 17 beta-estradiol in the proliferation of mcf7 an...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Medical hypotheses     Volume:  52     ISSN:  0306-9877     ISO Abbreviation:  Med. Hypotheses     Publication Date:  1999 Jun 
Date Detail:
Created Date:  1999-10-12     Completed Date:  1999-10-12     Revised Date:  2008-08-15    
Medline Journal Info:
Nlm Unique ID:  7505668     Medline TA:  Med Hypotheses     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  525-7     Citation Subset:  IM    
Affiliation:
Bristol-Myers Squibb, Pharmaceutical Research Institute, Seattle, Washington, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adult
Alzheimer Disease / pathology*
Cell Cycle*
Humans
Models, Neurological*
Nerve Degeneration*

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


Previous Document:  On ring chromatids.
Next Document:  Cysteine, glutathione (GSH) and zinc and copper ions together are effective, natural, intracellular ...