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胰岛素和氨基酸信号在调控虹鳟肝脏代谢相关基因表达中的整合:TOR 的作用。

Integration of insulin and amino acid signals that regulate hepatic metabolism-related gene expression in rainbow trout: role of TOR.

机构信息

INRA, UMR1067 Nutrition Aquaculture et Génomique, Pôle d'hydrobiologie, CD918, 64310, St Pée-sur-Nivelle, France.

出版信息

Amino Acids. 2010 Aug;39(3):801-10. doi: 10.1007/s00726-010-0533-3. Epub 2010 Mar 6.

Abstract

Amino acids are considered to be regulators of metabolism in several species, and increasing importance has been accorded to the role of amino acids as signalling molecules regulating protein synthesis through the activation of the TOR transduction pathway. Using rainbow trout hepatocytes, we examined the ability of amino acids to regulate hepatic metabolism-related gene expression either alone or together with insulin, and the possible involvement of TOR. We demonstrated that amino acids alone regulate expression of several genes, including glucose-6-phosphatase, phosphoenolpyruvate carboxykinase, pyruvate kinase, 6-phospho-fructo-1-kinase and serine dehydratase, through an unknown molecular pathway that is independent of TOR activation. When insulin and amino acids were added together, a different pattern of regulation was observed that depended upon activation of the TOR pathway. This pattern included a dramatic up-regulation of lipogenic (fatty acid synthase, ATP-citrate lyase and sterol responsive element binding protein 1) and glycolytic (glucokinase, 6-phospho-fructo-1-kinase and pyruvate kinase) genes in a TOR-dependent manner. Regarding gluconeogenesis genes, only glucose-6-phosphatase was inhibited in a TOR-dependent manner by combination of insulin and amino acids and not by amino acids alone. This study is the first to demonstrate an important role of amino acids in combination with insulin in the molecular regulation of hepatic metabolism.

摘要

氨基酸被认为是几种物种代谢的调节剂,并且氨基酸作为通过激活 TOR 转导途径来调节蛋白质合成的信号分子的作用越来越受到重视。使用虹鳟鱼肝细胞,我们研究了氨基酸单独或与胰岛素一起调节与肝代谢相关的基因表达的能力,以及 TOR 的可能参与。我们证明,氨基酸单独通过独立于 TOR 激活的未知分子途径调节几种基因的表达,包括葡萄糖-6-磷酸酶、磷酸烯醇丙酮酸羧激酶、丙酮酸激酶、6-磷酸果糖-1-激酶和丝氨酸脱水酶。当胰岛素和氨基酸一起添加时,观察到一种依赖于 TOR 途径激活的不同调节模式。这种模式包括以 TOR 依赖性方式强烈地上调脂肪生成(脂肪酸合酶、ATP-柠檬酸裂解酶和固醇响应元件结合蛋白 1)和糖酵解(葡糖激酶、6-磷酸果糖-1-激酶和丙酮酸激酶)基因。关于糖异生基因,只有葡萄糖-6-磷酸酶在胰岛素和氨基酸的组合作用下以 TOR 依赖性方式被抑制,而不是单独的氨基酸。这项研究首次证明了氨基酸在与胰岛素联合调节肝代谢的分子机制中起着重要作用。

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