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AMP激活蛋白激酶和环磷酸腺苷依赖性蛋白激酶在肾上腺素诱导的大鼠脂肪细胞乙酰辅酶A羧化酶失活中的作用。

Roles of the AMP-activated and cyclic-AMP-dependent protein kinases in the adrenaline-induced inactivation of acetyl-CoA carboxylase in rat adipocytes.

作者信息

Haystead T A, Moore F, Cohen P, Hardie D G

机构信息

Biochemistry Department, The University, Dundee, Scotland.

出版信息

Eur J Biochem. 1990 Jan 12;187(1):199-205. doi: 10.1111/j.1432-1033.1990.tb15295.x.

Abstract
  1. In isolated rat adipocytes, acetyl-CoA carboxylase is inactivated by treatment of the cells with adrenaline or the beta-agonist isoproterenol, but not by the alpha-agonist phenylephrine. The inactivation is stable during purification in the presence of protein phosphatase inhibitors, and is associated with a 30-40% increase in the labelling of enzyme isolated from 32P-labelled cells. 2. Increased phosphorylation occurs within peptide T1, which was identified by sequencing to be the peptide Ser-Ser77-Met-Ser79-Gly-Leu-His-Leu-Val-Lys, containing Ser-77 (phosphorylated by cyclic-AMP-dependent protein kinase) and Ser-79 (phosphorylated by the AMP-activated protein kinase). Analysis of the release of radioactivity as free phosphate during Edman degradation of peptide T1 revealed that all of the phosphate was in Ser-79 in both basal and hormone- or agonist-stimulated cells. Treatment of adipocytes with various agents which activate cyclic-AMP-dependent protein kinase by receptor-independent mechanisms (forskolin, cyclic AMP analogues, isobutylmethylxanthine) also produced inactivation of acetyl-CoA carboxylase and increased phosphorylation at Ser-79. 3. The (Rp)-[thio]phosphate analogue of cyclic AMP, which is an antagonist of binding of cyclic AMP to the regulatory subunit of cyclic-AMP-dependent protein kinase, opposes the effect of adrenaline on phosphorylation and inactivation of acetyl-CoA carboxylase. Together with the effects of isobutylmethylxanthine and the stimulatory cyclic AMP analogues, this strongly indicates that cyclic-AMP-dependent protein kinase is an essential component of the signal transduction pathway, although clearly it does not directly phosphorylate acetyl-CoA carboxylase. 4. As shown by okadaic acid inhibition, greater than 95% of the acetyl-CoA carboxylase phosphatase activity in extracts of rat adipocytes or liver is accounted for by protein phosphatase-2A, with less than 5% attributable to protein phosphatase-1. Inhibition of protein phosphatase-1 via phosphorylation of inhibitor-1 is therefore unlikely to be the mechanism by which cyclic-AMP-dependent protein kinase indirectly increases phosphorylation of acetyl-CoA carboxylase. Various other potential mechanisms are discussed.
摘要
  1. 在分离的大鼠脂肪细胞中,用肾上腺素或β-激动剂异丙肾上腺素处理细胞可使乙酰辅酶A羧化酶失活,但α-激动剂去氧肾上腺素则无此作用。在存在蛋白磷酸酶抑制剂的情况下进行纯化时,这种失活状态是稳定的,并且与从32P标记细胞中分离出的酶的标记增加30 - 40%相关。2. 肽段T1内发生磷酸化增加,经测序确定该肽段为Ser-Ser77-Met-Ser79-Gly-Leu-His-Leu-Val-Lys,包含Ser-77(由环磷酸腺苷依赖性蛋白激酶磷酸化)和Ser-79(由AMP激活的蛋白激酶磷酸化)。在肽段T1的埃德曼降解过程中,作为游离磷酸盐的放射性释放分析表明,在基础状态以及激素或激动剂刺激的细胞中,所有的磷酸盐都存在于Ser-79中。用各种通过非受体依赖机制激活环磷酸腺苷依赖性蛋白激酶的试剂(福斯高林、环磷酸腺苷类似物、异丁基甲基黄嘌呤)处理脂肪细胞,也会导致乙酰辅酶A羧化酶失活,并使Ser-79处的磷酸化增加。3. 环磷酸腺苷的(Rp)-[硫代]磷酸类似物是环磷酸腺苷与环磷酸腺苷依赖性蛋白激酶调节亚基结合的拮抗剂,它能对抗肾上腺素对乙酰辅酶A羧化酶磷酸化和失活的作用。连同异丁基甲基黄嘌呤和刺激性环磷酸腺苷类似物的作用,这有力地表明环磷酸腺苷依赖性蛋白激酶是信号转导途径的一个重要组成部分,尽管显然它并不直接使乙酰辅酶A羧化酶磷酸化。4. 如冈田酸抑制实验所示,大鼠脂肪细胞或肝脏提取物中超过95%的乙酰辅酶A羧化酶磷酸酶活性由蛋白磷酸酶-2A负责,而蛋白磷酸酶-1的贡献不到5%。因此,通过抑制剂-1的磷酸化来抑制蛋白磷酸酶-1不太可能是环磷酸腺苷依赖性蛋白激酶间接增加乙酰辅酶A羧化酶磷酸化的机制。文中还讨论了其他各种潜在机制。

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