The role of osteopontin in recovery from hind limb ischemia

被引:45
|
作者
Duvall, Craig L. [2 ,5 ]
Weiss, Daiana [1 ]
Robinson, Scott T. [2 ,5 ]
Alameddine, Fadi M. F. [1 ]
Guldberg, Robert E. [2 ,3 ,5 ]
Taylor, W. Robert [1 ,2 ,4 ,5 ]
机构
[1] Emory Univ, Sch Med, Div Cardiol, Dept Med, Atlanta, GA 30322 USA
[2] Georgia Inst Technol, Wallace H Cooulter Dept Biomed Engn, Atlanta, GA 30332 USA
[3] Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
[4] Vet Affairs Med Ctr, Decatur, GA 30033 USA
[5] Emory Univ, Wallace H Coluler Dept Biomed Engn, Atlanta, GA 30322 USA
关键词
osteopontin; hind limb ischemia; angiogenesis; arteriogenesis; collateral;
D O I
10.1161/ATVBAHA.107.158485
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-Osteopontin (OPN) is a highly phosphorylated extracellular matrix glycoprotein that is involved in a diversity of biological processes. In the vascular wall, OPN is produced by monocytes/macrophages, endothelial cells, and smooth muscle cells, and it is thought to mediate adhesion, migration, and survival of these cell types. In this study, we hypothesized that OPN plays a critical role in recovery from limb ischemia. Methods and Results-We induced hind limb ischemia in wild-type and OPN-/- mice. OPN-/- mice exhibited significantly delayed recovery of ischemic foot perfusion as determined by LDPI, impaired collateral vessel formation as measured using micro-CT, and diminished functional capacity of the ischemic limb. In the aortic ring assay, normal endothelial cell sprouting was found in OPN-/- mice. However, OPN-/- peritoneal monocytes/macrophages were found to possess significantly reduced migration in response to chemoattraction. Conclusions-This study provides evidence that a definitive biological role exists for OPN during ischemic limb revascularization, and we have suggested that this may be driven by impaired monocyte/macrophage migration in OPN-/- mice. These findings provide the first in vivo evidence that OPN may be a key regulator in postnatal vascular growth.
引用
收藏
页码:290 / 295
页数:6
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