Home LiteratureArticle Details
PMID: 12114325 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Osteopontin plays an important role in the development of medial thickening and neointimal formation.

Circulation research ·Vol. 91 ·No. 1 ·2002-07-12 ·Pages 77-82

Isoda K, Nishikawa K, Kamezawa Y, Yoshida M, Kusuhara M, Moroi M, Tada N, Ohsuzu F

Abstract

Osteopontin (OPN) is a soluble secreted phosphoprotein that binds with high affinity to several integrins and it has been found at the site of atherosclerotic lesions. However, the role of OPN expression in vivo is still poorly understood. To investigate the physiological role of OPN in detail, we generated transgenic mice (Tg) overexpressing the OPN gene under control of the cytomegalovirus enhancer/chicken beta-actin promoter. We detected OPN mRNAs in almost all tissues of 3 lines of Tg mice by Northern blotting. The serum levels of OPN were significantly higher in Tg than in non-Tg mice (782+/-107 versus 182+/-44 ng/mL; P<0.001). Compared with non-Tg mice, a 73% (88+/-6 versus 51+/-7 microm; P<0.001) and 94% (126+/-15 versus 73+/-11 microm; P<0.0001) increase in the medial thickness of the aorta was determined in Tg mice at 16 and 32 weeks after birth. However, we found no evidence of inflammatory cells adhering to endothelial cells, intimal hyperplasia, or calcification in any region of Tg mice without artery injury. We then investigated the effect of cuff-induced injury to the femoral artery. The intimal thickening in Tg mice increased 2.9-fold more than that in non-Tg mice (4.9+/-1.9 versus 1.7+/-0.4 microm; P=0.022). The expression of OPN induces both medial thickening without injury and neointimal formation after injury, thus suggesting that OPN plays a role in the development of atherosclerosis, vascular remodeling, and restenosis after angioplasty in vivo.

MeSH Terms
Animals Aorta/metabolism,pathology,physiopathology Cell Movement/physiology Female Femoral Artery/injuries Gene Expression Immunohistochemistry Male Matrix Metalloproteinase 2/metabolism Matrix Metalloproteinase 9/metabolism Mice Mice, Inbred C57BL Mice, Inbred Strains Mice, Transgenic Muscle, Smooth, Vascular/cytology Osteopontin Proliferating Cell Nuclear Antigen/analysis RNA, Messenger/genetics,metabolism Sialoglycoproteins/genetics,physiology Tunica Intima/metabolism,pathology,physiopathology Tunica Media/metabolism,pathology,physiopathology
Chemicals
Proliferating Cell Nuclear Antigen RNA, Messenger Sialoglycoproteins Spp1 protein, mouse Osteopontin Matrix Metalloproteinase 2 Matrix Metalloproteinase 9
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Isoda Kikuo
First Department of Internal Medicine, National Defense Medical College, Tokorozawa, Saitama, Japan. isoda@me.ndmc.ac.jp
Nishikawa Kenichirou
Kamezawa Yashuhiro
Yoshida Mikoto
Kusuhara Masatoshi
Moroi Masao
Tada Norihiro
Ohsuzu Fumitaka
Article Info
Journal
Circulation research
Abbr.
Circ Res
ISSN
1524-4571
Published
2002-07-12
Pages
77-82
Language
English
Region
United States
NLM ID
0047103
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com