Document Detail


Co-cultures of human coronary smooth muscle cells and dimethyl sulfoxide-differentiated HL60 cells upregulate ProMMP9 activity and promote mobility-modulation by reactive oxygen species.
MedLine Citation:
PMID:  18665441     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Vascular cells and leukocytes, involved in the development of atherosclerosis, produce cytokines and/or reactive oxygen species (ROS) and matrix metalloproteinases (MMPs) implicated in cell mobility. We investigated by co-culture experiments the effects of human coronary smooth muscle cells (HCSMC) on MMPs characteristics and mobility of neutrophil-like dimethyl sulfoxide-differentiated HL60 cells (not equal HL60). The effects of superoxide dismutase (SOD) and catalase were also analyzed. All the studied MMP2 characteristics remained unchanged. HCSMC stimulated MMP9 protein level, activity and mobility of not equal HL60 cells and expressed and secreted a variety of cytokines implicated in atherosclerosis. SOD and catalase increased MMP9 expression, protein level and activity of not equal HL60, but migration of not equal HL60 cells was only decreased by catalase, demonstrating that ROS are more efficient in modulating MMP9 activity of not equal HL60 than their mobility. Finally, HCSMC being able to stimulate not equal HL60, their co-cultures may represent an in vitro approach to study cellular interactions occurring in vivo during atherosclerosis.
Authors:
Yohann Bernard; Chantal Melchior; Eric Tschirhart; Jean-Luc Bueb
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Inflammation     Volume:  31     ISSN:  0360-3997     ISO Abbreviation:  Inflammation     Publication Date:  2008 Oct 
Date Detail:
Created Date:  2008-10-02     Completed Date:  2008-12-04     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7600105     Medline TA:  Inflammation     Country:  United States    
Other Details:
Languages:  eng     Pagination:  287-98     Citation Subset:  IM    
Affiliation:
Life Sciences Research Unit, Université du Luxembourg, 162a, Avenue de la Faïencerie, 1511 Luxembourg, Luxembourg.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Antioxidants / metabolism
Atherosclerosis / metabolism*
Cells, Cultured
Coculture Techniques*
Dimethyl Sulfoxide / pharmacology*
Gene Expression Regulation, Enzymologic*
HL-60 Cells
Humans
Inflammation
Matrix Metalloproteinase 9 / metabolism*
Models, Biological
Myocardium / metabolism*
Myocytes, Smooth Muscle / cytology*
Oxidative Stress
RNA, Messenger / metabolism
Chemical
Reg. No./Substance:
0/Antioxidants; 0/RNA, Messenger; 67-68-5/Dimethyl Sulfoxide; EC 3.4.24.35/Matrix Metalloproteinase 9

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


Previous Document:  Effects of fulminant hepatic encephalopathy on the adult rat brain antioxidant status and the activi...
Next Document:  Effects of rosiglitazone on the proliferation of vascular smooth muscle cell induced by high glucose...