Kruppel-like Factor 15 Regulates Smooth Muscle Response to Vascular Injury-Brief Report

被引:26
|
作者
Lu, Yuan [1 ]
Haldar, Saptarsi [1 ]
Croce, Kevin [2 ]
Wang, Yunmei [1 ]
Sakuma, Mashashi [1 ]
Morooka, Toshifumi [1 ]
Wang, Baiqiu [1 ]
Jeyaraj, Darwin [1 ]
Gray, Susan J.
Simon, Daniel I. [1 ]
Jain, Mukesh K. [1 ]
机构
[1] Case Western Reserve Univ, Sch Med, Univ Hosp Harrington McLaughlin Heart & Vasc Inst, Univ Hosp Case Med Ctr,Dept Med,Case Cardiovasc R, Cleveland, OH 44106 USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Cardiovasc, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
KLF15; smooth muscle; vascular injury; proliferation; migration; NEOINTIMAL FORMATION; CELL-GROWTH; PROLIFERATION; KRUPPEL-LIKE-FACTOR-15; MIGRATION;
D O I
10.1161/ATVBAHA.110.207050
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To determine the role of Kruppel-like factor (KLF) 15, a zinc finger transcriptional factor that is expressed in vascular smooth muscle cells (VSMCs) in vascular biology. VSMCs respond to mechanical injury via a tightly orchestrated series of gene regulatory events. KLF15 is broadly expressed in both arterial and venous vascular beds in a VSMC restricted fashion. KLF15 expression is markedly reduced by both pharmacological and mechanical stimuli. To examine the specific role of KLF15 in the vascular response to injury, we performed femoral artery wire injury in KLF15(-/-) and wild-type mice. KLF15(-/-) mice develop exaggerated neointimal growth, with evidence of increased SMC proliferation and migration within the neointima. In concordance, gain and loss of function studies in isolated VSMCs demonstrate that KLF15 can directly inhibit SMC proliferation and migration. To our knowledge, these data are the first to identify KLF15 as a novel inhibitor of VSMC proliferation and migration and to implicate this factor as a critical regulator of the vascular response to injury. (Arterioscler Thromb Vasc Biol. 2010;30:1550-1552.)
引用
收藏
页码:1550 / U83
页数:9
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