Krüppel-like factor 4 regulates pressure-induced cardiac hypertrophy

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• 作者：Xudong Liao ; Saptarsi M. Haldar ; Yuan Lu ; Darwin Jeyaraj ; Kaavya Paruchuri ; Monika Nahori ; Yingjie Cui ; Klaus H. Kaestner ; Mukesh K. Jain
• 关键词：Kr&#xfc ; ppel ; Hypertrophy ; Myocyte ; Transcription ; Pressure overload
• 刊名：Journal of Molecular and Cellular Cardiology
• 出版年：2010
• 出版时间：August 2010
• 年：2010
• 卷：49
• 期：2
• 页码：334-338
• 全文大小：845 K

文摘

Krüppel-like factors (KLF) are a subfamily of the zinc-finger class of transcriptional regulators that play important roles in diverse cellular processes. While a number of KLFs are expressed in cardiomyocytes, little is known about their specific roles in the heart in vivo. Here, we demonstrate that KLF4 is induced by hypertrophic stimuli in cultured cardiomyocytes and in the mouse heart. Overexpression of KLF4 in neonatal rat ventricular myocytes inhibits three cardinal features of cardiomyocyte hypertrophy: fetal gene expression, protein synthesis, and cell enlargement. Conversely, mice with cardiomyocyte-specific deletion of KLF4 (CM-K4KO) are highly sensitized to transverse aortic constriction (TAC) and exhibit high rates of mortality. CM-K4KO mice that survive TAC display severe pathologic cardiac hypertrophy characterized by increased cardiac mass, depressed LV systolic function, pulmonary congestion, cavity dilation and attenuated LV wall thickening when compared to control genotypes. In addition, CM-K4KO mice develop increased myocardial fibrosis and apoptotic cell death after TAC. Collectively, these studies implicate KLF4 as a novel transcriptional regulator that is indispensible for the heart's response to stress in vivo.