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心脏ERK1/2的基因抑制促进应激诱导的细胞凋亡和心力衰竭,但对体内肥大无影响。

Genetic inhibition of cardiac ERK1/2 promotes stress-induced apoptosis and heart failure but has no effect on hypertrophy in vivo.

作者信息

Purcell Nicole H, Wilkins Benjamin J, York Allen, Saba-El-Leil Marc K, Meloche Sylvain, Robbins Jeffrey, Molkentin Jeffery D

机构信息

Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.

出版信息

Proc Natl Acad Sci U S A. 2007 Aug 28;104(35):14074-9. doi: 10.1073/pnas.0610906104. Epub 2007 Aug 20.

Abstract

MAPK signaling pathways function as critical regulators of cellular differentiation, proliferation, stress responsiveness, and apoptosis. One branch of the MAPK signaling pathway that culminates in ERK1/2 activation is hypothesized to regulate the growth and adaptation of the heart to both physiologic and pathologic stimuli, given its known activation in response to virtually every stress- and agonist-induced hypertrophic stimulus examined to date. Here we investigated the requirement of ERK1/2 signaling in mediating the cardiac hypertrophic growth response in Erk1(-/-) and Erk2(+/-) mice, as well as in transgenic mice with inducible expression of an ERK1/2-inactivating phosphatase in the heart, dual-specificity phosphatase 6. Although inducible expression of dual-specificity phosphatase 6 in the heart eliminated ERK1/2 phosphorylation at baseline and after stimulation without affecting any other MAPK, it did not diminish the hypertrophic response to pressure overload stimulation, neuroendocrine agonist infusion, or exercise. Similarly, Erk1(-/-) and Erk2(+/-) mice showed no reduction in pathologic or physiologic stimulus-induced cardiac growth in vivo. However, blockade or deletion of cardiac ERK1/2 did predispose the heart to decompensation and failure after long-term pressure overload in conjunction with an increase in myocyte TUNEL. Thus, ERK1/2 signaling is not required for mediating physiologic or pathologic cardiac hypertrophy in vivo, although it does play a protective role in response to pathologic stimuli.

摘要

丝裂原活化蛋白激酶(MAPK)信号通路是细胞分化、增殖、应激反应和细胞凋亡的关键调节因子。鉴于迄今为止在几乎所有应激和激动剂诱导的肥大刺激下均已知其被激活,MAPK信号通路中最终导致ERK1/2激活的一个分支被认为可调节心脏对生理和病理刺激的生长及适应性。在此,我们研究了ERK1/2信号在介导Erk1基因敲除小鼠和Erk2杂合小鼠以及心脏中可诱导表达ERK1/2失活磷酸酶双特异性磷酸酶6的转基因小鼠的心脏肥大生长反应中的作用。尽管在心脏中可诱导表达双特异性磷酸酶6可消除基线和刺激后的ERK1/2磷酸化,且不影响任何其他MAPK,但它并未减弱对压力超负荷刺激、神经内分泌激动剂输注或运动的肥大反应。同样,Erk1基因敲除小鼠和Erk2杂合小鼠在体内对病理或生理刺激诱导的心脏生长也未表现出减少。然而,阻断或缺失心脏中的ERK1/2确实会使心脏在长期压力超负荷后易发生失代偿和衰竭,同时心肌细胞TUNEL增加。因此,ERK1/2信号在体内介导生理性或病理性心脏肥大并非必需,尽管它在应对病理刺激时确实发挥保护作用。

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