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骨骼肌的机械刺激通过磷脂酶激活产生脂质相关的第二信使。

Mechanical stimulation of skeletal muscle generates lipid-related second messengers by phospholipase activation.

作者信息

Vandenburgh H H, Shansky J, Karlisch P, Solerssi R L

机构信息

Department of Pathology, Brown University, Providence, Rhode Island 02912.

出版信息

J Cell Physiol. 1993 Apr;155(1):63-71. doi: 10.1002/jcp.1041550109.

Abstract

Repetitive mechanical stimulation of cultured avian skeletal muscle increases the synthesis of prostaglandins (PG) E2 and F2 alpha which regulate protein turnover rates and muscle cell growth. These stretch-induced PG increases are reduced in low extracellular calcium medium and by specific phospholipase inhibitors. Mechanical stimulation increases the breakdown rate of 3H-arachidonic acid labelled phospholipids, releasing free 3H-arachidonic acid, the rate-limiting precursor of PG synthesis. Mechanical stimulation also increases 3H-arachidonic acid labelled diacylglycerol formation and intracellular levels of inositol phosphates from myo-[2-3H]inositol labelled phospholipids. Phospholipase A2 (PLA2), phosphatidylinositol-specific phospholipase C (PLC), and phospholipase D (PLD) are all activated by stretch. The stretch-induced increases in PG production, 3H-arachidonic acid labelled phospholipid breakdown, and 3H-arachidonic acid labelled diacylglycerol formation occur independently of cellular electrical activity (tetrodotoxin insensitive) whereas the formation of inositol phosphates from myo-[2-3H]inositol labelled phospholipids is dependent on cellular electrical activity. These results indicate that mechanical stimulation increases the lipid-related second messengers arachidonic acid, diacylglycerol, and PG through activation of specific phospholipases such as PLA2 and PLD, but not by activation of phosphatidylinositol-specific PLC.

摘要

对培养的禽骨骼肌进行重复性机械刺激可增加前列腺素(PG)E2和F2α的合成,而这些前列腺素可调节蛋白质周转率和肌肉细胞生长。在低细胞外钙培养基中以及使用特定的磷脂酶抑制剂时,这些拉伸诱导的PG增加会减少。机械刺激会增加3H-花生四烯酸标记的磷脂的分解速率,释放出游离的3H-花生四烯酸,而3H-花生四烯酸是PG合成的限速前体。机械刺激还会增加3H-花生四烯酸标记的二酰基甘油的形成以及来自肌醇-[2-3H]肌醇标记的磷脂的细胞内肌醇磷酸水平。磷脂酶A2(PLA2)、磷脂酰肌醇特异性磷脂酶C(PLC)和磷脂酶D(PLD)都会因拉伸而被激活。拉伸诱导的PG产生增加、3H-花生四烯酸标记的磷脂分解以及3H-花生四烯酸标记的二酰基甘油形成与细胞电活动无关(对河豚毒素不敏感),而来自肌醇-[2-3H]肌醇标记的磷脂的肌醇磷酸形成则依赖于细胞电活动。这些结果表明,机械刺激通过激活特定的磷脂酶(如PLA2和PLD)来增加与脂质相关的第二信使花生四烯酸、二酰基甘油和PG,而不是通过激活磷脂酰肌醇特异性PLC来实现。

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