cMyBP-C was decreased via KLHL3-mediated proteasomal degradation in congenital heart diseases
cMyBP-C was decreased via KLHL3-mediated proteasomal degradation in congenital heart diseases
复制标题
先天性心脏病中 cMyBP-C 通过 KLHL3 介导的蛋白酶体降解而减少
DOI:
10.1016/j.yexcr.2017.03.025
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发表时间:
2017
影响因子:
3.7
通讯作者:
Zhao Yanyan
中科院分区:
文献类型:
--
作者:
Wang Leitong;Lai Guangrui;Chu Guoming;Liang Xiaoyan;Zhao Yanyan
Cardiac myosin binding protein C (cMyBP-C) is a cardiac structural and regulatory protein; mutations of cMyBP-C are frequently associated with hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM). Cardiac special transcription factors may regulate the expression of cMyBP-C. However, the role of cMyBP-C in congenital heart diseases (CHD) remains poorly understood. In the current study, western blotting and the MRM approach showed that cMyBP-C expression was significantly reduced in fetuses with CHD compared to those without. Furthermore, we found that cMyBP-C interacted with KLHL3 by immunoprecipitation and immunofluorescence, and the degradation of cMyBP-C was caused by KLHL3-mediated ubiquitination. In addition, homocysteine (Hcy, a risk factor of CHD) treatment caused a decrease in cMyBP-C and an increase in KLHL3 expression, and the proteasome inhibitor MG132 reversed the Hcy-induced reduction of cMyBP-C expression. Finally, we verified that reduced cMyBP-C by Hcy promoted apoptosis in cardiomyocytes. These results demonstrate that Hcy decreases the expression of cMyBP-C through a KLHL3-mediated ubiquitin–proteasome pathway, and thereby influences heart development.