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磷酸肌醇3激酶抑制剂对自噬蛋白水解作用的抑制会干扰离体肝细胞中糖原合成的调节。

Inhibition of autophagic proteolysis by inhibitors of phosphoinositide 3-kinase can interfere with the regulation of glycogen synthesis in isolated hepatocytes.

作者信息

Dubbelhuis Peter F, Van Sluijters Daphne A, Blommaart Edward F C, Gustafson Lori A, Van Woerkom George M, Herling Andreas W, Burger Hans-Joerg, Meijer Alfred J

机构信息

Department of Biochemistry, Academic Medical Center, University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands.

出版信息

Biochem J. 2002 Dec 15;368(Pt 3):827-33. doi: 10.1042/BJ20021340.

Abstract

Amino acid-induced cell swelling stimulates conversion of glucose into glycogen in isolated hepatocytes. Activation of glycogen synthase (GS) phosphatase, caused by the fall in intracellular chloride accompanying regulatory volume decrease, and activation of phosphoinositide 3-kinase (PI 3-kinase), induced by cell swelling, have been proposed as underlying mechanisms. Because PI 3-kinase controls autophagic proteolysis, we examined the possibility that PI 3-kinase inhibitors interfere with glycogen production due to their anti-proteolytic action. The PI 3-kinase inhibitor wortmannin inhibited endogenous proteolysis, the production of glycogen from glucose and the activity of active (dephosphorylated) GS (GS a ) in the absence of added amino acids. The stimulation by amino acids of glycogen production and of GS a was only slightly affected by wortmannin. These effects of wortmannin could be mimicked by proteinase inhibitors. A combination of leucine, phenylalanine and tyrosine, which we showed previously to stimulate PI 3-kinase-dependent phosphorylation of ribosomal protein S6, did not stimulate glycogen production from glucose. In contrast with wortmannin, LY294002, another PI 3-kinase inhibitor, strongly inhibited both glycogen synthesis and GS a activity, irrespective of the presence of amino acids. Inhibition of glycogen synthesis by LY294002 could be ascribed in part to increased glycogenolysis and glycolysis. It is concluded that, in hepatocytes, activation of PI 3-kinase may not be responsible for the stimulation of glycogen synthesis by amino acids; LY294002 inhibits glycogen synthesis and stimulates glycogen breakdown by a mechanism that is unrelated to its action as an inhibitor of PI 3-kinase.

摘要

氨基酸诱导的细胞肿胀可刺激分离的肝细胞将葡萄糖转化为糖原。细胞肿胀引起细胞内氯离子浓度下降,进而激活糖原合酶(GS)磷酸酶,同时细胞肿胀诱导磷酸肌醇3激酶(PI 3激酶)的激活,这些被认为是潜在的机制。由于PI 3激酶控制自噬性蛋白水解,我们研究了PI 3激酶抑制剂因其抗蛋白水解作用而干扰糖原生成的可能性。在未添加氨基酸的情况下,PI 3激酶抑制剂渥曼青霉素抑制内源性蛋白水解、葡萄糖生成糖原以及活性(去磷酸化)GS(GS a)的活性。渥曼青霉素对氨基酸刺激糖原生成和GS a的作用仅有轻微影响。渥曼青霉素的这些作用可被蛋白酶抑制剂模拟。亮氨酸、苯丙氨酸和酪氨酸的组合(我们之前表明其可刺激核糖体蛋白S6的PI 3激酶依赖性磷酸化)并不能刺激葡萄糖生成糖原。与渥曼青霉素不同,另一种PI 3激酶抑制剂LY294002强烈抑制糖原合成和GS a活性,无论是否存在氨基酸。LY294002对糖原合成的抑制部分可归因于糖原分解和糖酵解增加。结论是,在肝细胞中,PI 3激酶的激活可能与氨基酸刺激糖原合成无关;LY294002通过一种与其作为PI 3激酶抑制剂的作用无关的机制抑制糖原合成并刺激糖原分解。

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