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KLF2 和 KLF4 控制着内皮细胞的特性和血管的完整性。

KLF2 and KLF4 control endothelial identity and vascular integrity.

机构信息

Cardiovascular Research Institute, Department of Medicine, and.

Department of Physiology and Biophysics, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.

出版信息

JCI Insight. 2017 Feb 23;2(4):e91700. doi: 10.1172/jci.insight.91700.

Abstract

Maintenance of vascular integrity in the adult animal is needed for survival, and it is critically dependent on the endothelial lining, which controls barrier function, blood fluidity, and flow dynamics. However, nodal regulators that coordinate endothelial identity and function in the adult animal remain poorly characterized. Here, we show that endothelial KLF2 and KLF4 control a large segment of the endothelial transcriptome, thereby affecting virtually all key endothelial functions. Inducible endothelial-specific deletion of and/or reveals that a single allele of either gene is sufficient for survival, but absence of both (EC-DKO) results in acute death from myocardial infarction, heart failure, and stroke. EC-DKO animals exhibit profound compromise in vascular integrity and profound dysregulation of the coagulation system. Collectively, these studies establish an absolute requirement for KLF2/4 for maintenance of endothelial and vascular integrity in the adult animal.

摘要

维持成年动物的血管完整性对于生存至关重要,而这严重依赖于内皮细胞层,其控制着屏障功能、血液流动性和血流动力学。然而,协调成年动物内皮细胞特性和功能的节点调节剂仍未得到充分描述。在这里,我们发现内皮细胞 KLF2 和 KLF4 控制了大部分内皮细胞转录组,从而影响了几乎所有关键的内皮细胞功能。内皮细胞特异性诱导型敲除 和/或 表明,单个基因的一个等位基因足以存活,但两个基因都缺失(EC-DKO)会导致急性心肌梗死、心力衰竭和中风导致死亡。EC-DKO 动物表现出血管完整性的严重损伤和凝血系统的严重失调。总的来说,这些研究确立了 KLF2/4 在维持成年动物内皮细胞和血管完整性方面的绝对必要性。

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