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本文引用的文献

1
Sphingosine-1-phosphate receptor-2 regulates expression of smooth muscle alpha-actin after arterial injury.1-磷酸鞘氨醇受体-2调节动脉损伤后平滑肌α-肌动蛋白的表达。
Arterioscler Thromb Vasc Biol. 2009 Oct;29(10):1644-50. doi: 10.1161/ATVBAHA.109.191965. Epub 2009 Jul 16.
2
Kruppel-like factor 5 shows proliferation-specific roles in vascular remodeling, direct stimulation of cell growth, and inhibition of apoptosis.Kruppel样因子5在血管重塑、直接刺激细胞生长和抑制细胞凋亡中发挥增殖特异性作用。
J Biol Chem. 2009 Apr 3;284(14):9549-57. doi: 10.1074/jbc.M806230200. Epub 2009 Feb 3.
3
Dominant-negative loss of PPARgamma function enhances smooth muscle cell proliferation, migration, and vascular remodeling.PPARγ功能的显性负性缺失增强了平滑肌细胞的增殖、迁移和血管重塑。
Arterioscler Thromb Vasc Biol. 2009 Apr;29(4):465-71. doi: 10.1161/ATVBAHA.109.184234. Epub 2009 Jan 29.
4
Conditional deletion of Krüppel-like factor 4 delays downregulation of smooth muscle cell differentiation markers but accelerates neointimal formation following vascular injury.Krüppel样因子4的条件性缺失会延迟平滑肌细胞分化标志物的下调,但会加速血管损伤后的内膜增生。
Circ Res. 2008 Jun 20;102(12):1548-57. doi: 10.1161/CIRCRESAHA.108.176974. Epub 2008 May 15.
5
Kruppel-like factor 15 is a regulator of cardiomyocyte hypertrophy.Kruppel样因子15是心肌细胞肥大的调节因子。
Proc Natl Acad Sci U S A. 2007 Apr 24;104(17):7074-9. doi: 10.1073/pnas.0701981104. Epub 2007 Apr 16.
6
Kruppel-like factor 4 abrogates myocardin-induced activation of smooth muscle gene expression.Kruppel样因子4消除心肌素诱导的平滑肌基因表达激活。
J Biol Chem. 2005 Mar 11;280(10):9719-27. doi: 10.1074/jbc.M412862200. Epub 2004 Dec 28.
7
Krüppel-like zinc-finger transcription factor KLF5/BTEB2 is a target for angiotensin II signaling and an essential regulator of cardiovascular remodeling.类Krüppel锌指转录因子KLF5/BTEB2是血管紧张素II信号传导的靶点以及心血管重塑的关键调节因子。
Nat Med. 2002 Aug;8(8):856-63. doi: 10.1038/nm738. Epub 2002 Jul 8.
8
The Krüppel-like factor KLF15 regulates the insulin-sensitive glucose transporter GLUT4.类 Kruppel 因子 KLF15 调节胰岛素敏感性葡萄糖转运蛋白 GLUT4。
J Biol Chem. 2002 Sep 13;277(37):34322-8. doi: 10.1074/jbc.M201304200. Epub 2002 Jul 3.
9
Krüppel-like factors: three fingers in many pies.Krüppel样因子:涉足诸多领域的三指蛋白
J Biol Chem. 2001 Sep 14;276(37):34355-8. doi: 10.1074/jbc.R100043200. Epub 2001 Jul 6.

Kruppel 样因子 15 调节血管损伤后平滑肌的反应——简短报告。

Kruppel-like factor 15 regulates smooth muscle response to vascular injury--brief report.

机构信息

Case Cardiovascular Research Institute, Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.

出版信息

Arterioscler Thromb Vasc Biol. 2010 Aug;30(8):1550-2. doi: 10.1161/ATVBAHA.110.207050. Epub 2010 May 27.

DOI:10.1161/ATVBAHA.110.207050
PMID:20508206
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2937185/
Abstract

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.

摘要

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。