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热休克刺激哺乳动物细胞中花生四烯酸的释放以及前列腺素和白三烯B4的合成。

Heat shock stimulates the release of arachidonic acid and the synthesis of prostaglandins and leukotriene B4 in mammalian cells.

作者信息

Calderwood S K, Bornstein B, Farnum E K, Stevenson M A

机构信息

Joint Center for Radiation Therapy, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

J Cell Physiol. 1989 Nov;141(2):325-33. doi: 10.1002/jcp.1041410214.

Abstract

Heat shock has a profound influence on the metabolism and behavior of eukaryotic cells. We have examined the effects of heat shock on the release from cells of arachidonic acid and its bioactive eicosanoid metabolites, the prostaglandins and leukotrienes. Heat shock (42-45 degrees) increased the rate of arachidonic acid release from human, rat, murine, and hamster cells. Arachidonate accumulation appeared to be due, at least partially, to stimulation of a phospholipase A2 activity by heat shock and was accompanied by the accumulation of lysophosphatidyl-inositol and lysophosphatidylcholine in membranes. Induction of arachidonate release by heat did not appear to be mediated by an increase in cell Ca++. Stimulation of arachidonate release by heat shock in hamster fibroblasts was quantitatively similar to the receptor-mediated effects of alpha thrombin and bradykinin. The effects of heat shock and alpha thrombin on arachidonate release were inhibited by glucocorticoids. Increased arachidonate release in heat-shocked cells was accompanied by the accelerated accumulation of cyclooxygenase products prostaglandin E2 and prostaglandin F2 alpha and by 5-lipoxygenase metabolite leukotriene B4. Elevated concentrations of arachidonic acid and metabolites may be involved in the cytotoxic effects of hyperthermia, in homeostatic responses to heat shock, and in vascular and inflammatory reactions to stress.

摘要

热休克对真核细胞的代谢和行为具有深远影响。我们已经研究了热休克对细胞释放花生四烯酸及其生物活性类二十烷酸代谢产物(前列腺素和白三烯)的影响。热休克(42 - 45摄氏度)增加了人、大鼠、小鼠和仓鼠细胞中花生四烯酸的释放速率。花生四烯酸的积累似乎至少部分是由于热休克刺激了磷脂酶A2的活性,并且伴随着膜中溶血磷脂酰肌醇和溶血磷脂酰胆碱的积累。热诱导花生四烯酸释放似乎不是由细胞内钙离子增加介导的。热休克对仓鼠成纤维细胞中花生四烯酸释放的刺激在数量上与α凝血酶和缓激肽的受体介导效应相似。热休克和α凝血酶对花生四烯酸释放的影响受到糖皮质激素的抑制。热休克细胞中花生四烯酸释放增加伴随着环氧化酶产物前列腺素E2和前列腺素F2α以及5 - 脂氧合酶代谢产物白三烯B4的加速积累。花生四烯酸及其代谢产物浓度的升高可能参与了高温的细胞毒性作用、对热休克的稳态反应以及对压力的血管和炎症反应。

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