Title of article :
Expression of matrix Gla protein and osteonectin mRNA by human aortic smooth muscle cells
Author/Authors :
Hao، نويسنده , , Hiroyuki and Hirota، نويسنده , , Seiichi and Ishibashi-Ueda، نويسنده , , Hatsue and Kushiro، نويسنده , , Toshio and Kanmatsuse، نويسنده , , Katsuo and Yutani، نويسنده , , Chikao، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Pages :
8
From page :
195
To page :
202
Abstract :
Background data indicate that matrix proteins such as matrix Gla protein (MGP) and osteonectin (ON) influence not only mineralization of vasculature but smooth muscle cell (SMC) differentiation. s mined whether MGP and ON are expressed by human aortic SMCs in vivo using Northern blotting, in situ hybridization and immunohistochemistry. s d ON mRNAs were strongly expressed in the aorta without atherosclerosis from newborn and four young subjects up to 10 years old. In the aorta from 15 adult cases, MGP and ON mRNAs were decreased as atherosclerosis developed. We determined cell type and distribution of the MGP- and ON mRNA-expressing cells by in situ hybridization and immunohistochemistry. In the aorta obtained from newborn and young subjects, SMCs in the media and thin intima expressed MGP mRNA and, to a lesser extent, ON mRNA. In the adult aorta with fibrous thickening, MGP mRNA was expressed by intimal SMCs and subpopulation of medial SMCs. Osteonectin mRNA was expressed mainly by intimal SMCs and few medial SMCs. Double immunohistochemical staining revealed that both MGP- and ON protein-expressing cells were positive for anti-α-smooth muscle actin antibody, aortic SMCs. sions results suggested that MGP and ON expression by aortic SMCs might be regulated by the degree of atherosclerosis and SMC differentiation in human aorta.
Keywords :
mineralization , Fibrous thickening , Smooth muscle cell heterogeneity , Cell differentiation , Gene expression
Journal title :
Cardiovascular Pathology
Serial Year :
2004
Journal title :
Cardiovascular Pathology
Record number :
1844666
Link To Document :
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