Case Cardiovascular Research Institute, Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.
Arterioscler Thromb Vasc Biol. 2010 Aug;30(8):1550-2. doi: 10.1161/ATVBAHA.110.207050. Epub 2010 May 27.
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.
为了确定 Kruppel 样因子 15(KLF15)在血管生物学中的作用,KLF15 是一种锌指转录因子,在血管平滑肌细胞(VSMCs)中表达。VSMCs 通过一系列紧密协调的基因调控事件对机械损伤作出反应。KLF15 以 VSMC 受限的方式在动脉和静脉血管床中广泛表达。KLF15 的表达可被药理学和机械刺激显著降低。为了研究 KLF15 在血管损伤反应中的特定作用,我们在 KLF15(-/-)和野生型小鼠中进行了股动脉丝损伤。KLF15(-/-)小鼠表现出明显的新生内膜过度生长,新生内膜中可见平滑肌细胞增殖和迁移增加。一致地,在分离的 VSMCs 中进行的功能获得和功能丧失研究表明,KLF15 可以直接抑制平滑肌细胞的增殖和迁移。据我们所知,这些数据首次将 KLF15 鉴定为 VSMC 增殖和迁移的新型抑制剂,并表明该因子是血管对损伤反应的关键调节因子。