Mammalian target of rapamycin and protein kinase A signaling mediate the cardiac transcriptional response to glutamine

被引:55
作者
Xia, Y
Wen, HY
Young, ME
Guthrie, PH
Taegtmeyer, H
Kellems, RE
机构
[1] Univ Texas, Sch Med, Dept Biochem & Mol Biol, Houston, TX 77030 USA
[2] Univ Texas, Sch Med, Dept Internal Med, Houston, TX 77030 USA
关键词
D O I
10.1074/jbc.M208500200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The addition of glutamine as a major nutrient to cultured neonatal rat cardiomyocytes produced an increase in myocyte size and the organization of actin into myofibrillar arrays. The cellular response was associated with increased abundance of the mRNAs encoding the contractile proteins, a-myosin heavy chain and cardiac a-actin, and the metabolic enzymes, muscle carnitine palmitoyl transferase I and muscle adenylosuccinate synthetase (ADSS1). Adss1 gene expression was induced similar to5-fold in glutamine-treated rat neonatal cardiac myocytes. The induction was mediated through the protein kinase A and mammalian target of rapamycin signaling pathways and required a cyclic AMP response element associated with the promoter region of the Adss1 gene. These results highlight glutamine as a major nutrient regulator of cardiac gene expression and identify protein kinase A and mammalian target of rapamycin signaling pathways as mediators of the cardiomyocyte transcriptional response.
引用
收藏
页码:13143 / 13150
页数:8
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