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糖原合酶激酶-3:耐冻木蛙的冷冻保护和糖原代谢。

Glycogen synthase kinase-3: cryoprotection and glycogen metabolism in the freeze-tolerant wood frog.

机构信息

Micropharma Ltd, 141 President Kennedy Avenue, Université de Quebec à Montreal (UQAM), Biological Sciences Building Unit 5569, Montreal, QC, Canada, H2X 3Y7.

出版信息

J Exp Biol. 2012 Feb 1;215(Pt 3):543-51. doi: 10.1242/jeb.065961.

Abstract

The terrestrial anuran Rana sylvatica tolerates extended periods of whole-body freezing during the winter. Freezing survival is facilitated by extensive glycogen hydrolysis and distribution of high concentrations of the cryoprotectant glucose into blood and all tissues. As glycogenesis is both an energy-expensive process and counter-productive to maintaining sustained high cryoprotectant levels, we proposed that glycogen synthase kinase-3 (GSK-3) would be activated when wood frogs froze and would phosphorylate its downstream substrates to inactivate glycogen synthesis. Western blot analysis determined that the amount of phosphorylated (inactive) GSK-3 decreased in all five tissues tested in 24 h frozen frogs compared with unfrozen controls. Total GSK-3 protein levels did not change, with the exception of heart GSK-3, indicating that post-translational modification was the primary regulatory mechanism for this kinase. Kinetic properties of skeletal muscle GSK-3 from control and frozen frogs displayed differential responses to a temperature change (22 versus 4°C) and high glucose. For example, when assayed at 4°C, the K(m) for the GSK-3 substrate peptide was ∼44% lower for frozen frogs than the corresponding value in control frogs, indicating greater GSK-3 affinity for its substrates in the frozen state. This indicates that at temperatures similar to the environment encountered by frogs, GSK-3 in frozen frogs will phosphorylate its downstream targets more readily than in unfrozen controls. GSK-3 from skeletal muscle of control frogs was also allosterically regulated. AMP and phosphoenolpyruvate activated GSK-3 whereas inhibitors included glucose, glucose 6-phosphate, pyruvate, ATP, glutamate, glutamine, glycerol, NH(4)Cl, NaCl and KCl. The combination of phosphorylation and allosteric control argues for a regulatory role of GSK-3 in inactivating glycogenesis to preserve high glucose cryoprotectant levels throughout each freezing bout.

摘要

陆生蛙类林蛙能在冬季长时间忍受全身冻结。通过广泛的糖原水解和将高浓度的防冻剂葡萄糖分布到血液和所有组织中,实现了冷冻生存。由于糖异生既是一个能量消耗大的过程,又不利于维持持续的高防冻剂水平,因此我们提出,当林蛙冻结时,糖原合酶激酶-3(GSK-3)会被激活,其下游底物会被磷酸化而失活糖原合成。Western blot 分析确定,与未冻结对照相比,在 24 小时冷冻的青蛙的五个测试组织中,磷酸化(失活)GSK-3 的量减少。除了心脏 GSK-3 之外,总 GSK-3 蛋白水平没有变化,这表明这种激酶的主要调节机制是翻译后修饰。来自对照和冷冻青蛙的骨骼肌 GSK-3 的动力学特性对温度变化(22 与 4°C)和高葡萄糖表现出不同的反应。例如,在 4°C 下测定时,冷冻青蛙的 GSK-3 底物肽的 K(m)比对照青蛙的相应值低约 44%,表明在冷冻状态下 GSK-3 对其底物的亲和力更大。这表明,在类似于青蛙遇到的环境温度下,冷冻青蛙中的 GSK-3 将比未冷冻对照更易于磷酸化其下游靶标。来自对照青蛙骨骼肌的 GSK-3 也受到变构调节。AMP 和磷酸烯醇丙酮酸激活 GSK-3,而抑制剂包括葡萄糖、葡萄糖 6-磷酸、丙酮酸、ATP、谷氨酸、谷氨酰胺、甘油、NH 4 Cl、NaCl 和 KCl。磷酸化和变构调节的组合表明 GSK-3 在失活糖异生以在每次冻结过程中维持高葡萄糖防冻剂水平方面具有调节作用。

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