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昆虫脂肪动激素刺激肌醇磷酸代谢:肌醇-1,4,5-三磷酸和肌醇-1,3,4,5-四磷酸在信号转导中的作用?

Insect adipokinetic hormone stimulates inositol phosphate metabolism: roles for both Ins(1,4,5)P3 and Ins(1,3,4,5)P4 in signal transduction?

作者信息

Van Marrewijk W J, Van den Broek A T, Gielbert M L, Van der Horst D J

机构信息

Department of Experimental Zoology, Utrecht University, The Netherlands.

出版信息

Mol Cell Endocrinol. 1996 Sep 18;122(2):141-50. doi: 10.1016/0303-7207(96)03877-4.

Abstract

Adipokinetic hormones (AKHs) control the mobilization of energy reserves from the insect fat body as fuels for flight activity. As a part of our investigations on AKH signal transduction, we demonstrate in this study that the inositol lipid cycle may be involved in the action of AKH-I on fat body of the migratory locust. We show that [3H]inositol is incorporated into fat body phosphoinositides in vitro, whose hydrolysis leads to the formation of the following inositol phosphates (InsPs): Ins(1 and/or 3)P, Ins(4)P, Ins(1,3)P2, Ins(1,4)P2, Ins(3,4)P3, Ins(1,3,4)P3, Ins(1,4,5)P3 and Ins(1,3,4,5)P4. AKH stimulates the formation of these isomers, eliciting an increase in radioactivity of total InsPs already after 1 min. Mass measurements show that Ins(1,4,5)P3 levels are substantially enhanced by AKH, which is indicative of hormonal activation of phospholipase C. In cell-free tissue preparations, Ins(1,4,5)P3 is metabolized through dephosphorylation as well as further phosphorylation. Ins(1,3,4,5)P4 is dephosphorylated primarily to Ins(1,3,4)P3, although the ability for its reconversion to Ins(1,4,5)P3 suggests that in vivo Ins(1,3,4,5)P4 may function as a rapidly mobilizable pool for Ins(1,4,5)P3 generation. Metabolic pathways for the conversion of InsPs to inositol in the locust fat body are proposed.

摘要

脂肪动激素(AKHs)控制着昆虫脂肪体中能量储备的动员,为飞行活动提供燃料。作为我们对AKH信号转导研究的一部分,我们在本研究中证明,肌醇脂质循环可能参与了AKH-I对飞蝗脂肪体的作用。我们发现,[3H]肌醇在体外可掺入脂肪体磷酸肌醇中,其水解会导致以下肌醇磷酸(InsPs)的形成:Ins(1和/或3)P、Ins(4)P、Ins(1,3)P2、Ins(1,4)P2、Ins(3,4)P3、Ins(1,3,4)P3、Ins(1,4,5)P3和Ins(1,3,4,5)P4。AKH刺激这些异构体的形成,在1分钟后就会引起总InsPs放射性的增加。质量测量表明,AKH可显著提高Ins(1,4,5)P3的水平,这表明磷脂酶C被激素激活。在无细胞组织制剂中,Ins(1,4,5)P3通过去磷酸化以及进一步磷酸化进行代谢。Ins(1,3,4,5)P4主要去磷酸化为Ins(1,3,4)P3,尽管其重新转化为Ins(1,4,5)P3的能力表明,在体内Ins(1,3,4,5)P4可能作为Ins(1,4,5)P3生成的快速可动员池。本文提出了蝗虫脂肪体中InsPs转化为肌醇的代谢途径。

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