Document Detail


Phenotypic heterogeneity influences apoptotic susceptibility to retinoic acid and cis-platinum of rat arterial smooth muscle cells in vitro: Implications for the evolution of experimental intimal thickening.
MedLine Citation:
PMID:  11451739     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Rat aortic smooth muscle cells (SMCs) cultured from intimal thickening 15 days after endothelial injury (IT-15), unlike those of normal media, show a monolayered, epithelioid phenotype and high levels of cellular retinol binding protein-1 (CRBP). Epithelioid clones obtained from the normal media suggest a "mosaicism" of arterial SMCs. Intimal cell homeostasis from the balance of proliferation and apoptosis is critical for the progression of vascular lesions. All-trans retinoic acid (tRA) reduced [(3)H]thymidine incorporation and G(1)-->S phase progression of IT-15 and epithelioid clone but not of normal media and IT 60 days after injury (IT-60) SMCs. Hoechst staining, flow cytometry, and ligation-mediated polymerase chain reaction showed an increased susceptibility of IT-15 and epithelioid clone to tRA and cis-diaminedichloroplatinum II (CDDP)-induced apoptosis and cytotoxicity compared with normal media and IT-60 cells. The latter retained an increased susceptibility to tRA-induced apoptosis compared with normal media SMCs. tRA-induced apoptosis associated with an increased ratio of bax to bcl-2 by bax overexpression and cleavage of caspase-3. Anti-CRBP but not anti-IgG antibody prevented tRA-induced apoptosis and changes in related signaling molecules but not CDDP effects. Our findings support the relevant role of phenotypic heterogeneity in the determining proliferative as well as apoptotic behavior of arterial SMCs.
Authors:
A Orlandi; A Francesconi; D Cocchia; A Corsini; L G Spagnoli
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Arteriosclerosis, thrombosis, and vascular biology     Volume:  21     ISSN:  1524-4636     ISO Abbreviation:  Arterioscler. Thromb. Vasc. Biol.     Publication Date:  2001 Jul 
Date Detail:
Created Date:  2001-07-13     Completed Date:  2001-09-13     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9505803     Medline TA:  Arterioscler Thromb Vasc Biol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1118-23     Citation Subset:  IM    
Affiliation:
Institute of Anatomic Pathology, Tor Vergata University of Rome, Italy.
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MeSH Terms
Descriptor/Qualifier:
Animals
Aorta / cytology*
Apoptosis*
Arteriosclerosis / etiology,  metabolism,  pathology*
Blotting, Western
Cell Cycle
Cell Division / drug effects
Cell Survival / drug effects
Cells, Cultured
Cisplatin / pharmacology*
Cytoskeletal Proteins / metabolism
Fluorescent Antibody Technique
Male
Muscle, Smooth, Vascular / drug effects,  metabolism,  pathology*
Phenotype
Rats
Rats, Wistar
Tretinoin / pharmacology*
Chemical
Reg. No./Substance:
0/Cytoskeletal Proteins; 15663-27-1/Cisplatin; 302-79-4/Tretinoin

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


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