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
相关论文
共 41 条
[1]   Monocyte activation in angiogenesis and collateral growth in the rabbit hindlimb [J].
Arras, M ;
Ito, WD ;
Scholz, D ;
Winkler, B ;
Schaper, J ;
Schaper, W .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (01) :40-50
[2]   Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization [J].
Asahara, T ;
Masuda, H ;
Takahashi, T ;
Kalka, C ;
Pastore, C ;
Silver, M ;
Kearne, M ;
Magner, M ;
Isner, JM .
CIRCULATION RESEARCH, 1999, 85 (03) :221-228
[3]   A regulated interaction between α5β1 integrin and osteopontin [J].
Barry, ST ;
Ludbrook, SB ;
Murrison, E ;
Horgan, CMT .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 267 (03) :764-769
[4]  
Bayless KJ, 1998, J CELL SCI, V111, P1165
[5]  
BERGMANN CE, 2006, J LEUKOC BIOL
[6]   Matricellular proteins: an overview - Introduction [J].
Bornstein, P .
MATRIX BIOLOGY, 2000, 19 (07) :555-556
[7]   Exercise-induced hyperemia unmasks regional blood flow deficit in experimental hindlimb ischemia [J].
Brevetti, LS ;
Paek, R ;
Brady, SE ;
Hoffman, JIE ;
Sarkar, R ;
Messina, LM .
JOURNAL OF SURGICAL RESEARCH, 2001, 98 (01) :21-26
[8]   Identification of osteopontin as a novel ligand for the integrin α8β1 and potential roles for this integrin-ligand interaction in kidney morphogenesis [J].
Denda, S ;
Reichardt, LF ;
Müller, U .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (06) :1425-1435
[9]   Osteopontin as a means to cope with environmental insults: regulation of inflammation, tissue remodeling, and cell survival [J].
Denhardt, DT ;
Noda, M ;
O'Regan, AW ;
Pavlin, D ;
Berman, JS .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (09) :1055-1061
[10]   Quantitative microcomputed tomography analysis of collateral vessel development after ischemic injury [J].
Duvall, CL ;
Taylor, WR ;
Weiss, D ;
Guldberg, RE .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2004, 287 (01) :H302-H310