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白三烯D4诱导大鼠嗜碱性白血病细胞钙动员的同源脱敏作用

Leukotriene D4-induced homologous desensitization of calcium mobilization in rat basophilic leukemia cells.

作者信息

Winkler J D, Mong S, Crooke S T

机构信息

Department of Molecular Pharmacology, Smith Kline & French Laboratories, King of Prussia, Pennsylvania.

出版信息

J Pharmacol Exp Ther. 1988 Feb;244(2):449-55.

PMID:2831340
Abstract

Previous work from our laboratory demonstrated that RBL-1 cells express membrane receptors for leukotriene (LT)D4 and that agonist stimulation of these receptors results in mobilization of intracellular calcium ([Ca++]i). We have used this LTD4 receptor-mediated event to examine the effects of homologous desensitization in RBL-1 cells. Prior exposure of RBL-1 cells to LTD4 resulted in a 40% reduction in the amount of maximal [Ca++]i mobilization. This desensitization was concentration- and time-dependent, with an EC50 of 1 to 3 nM and with 50% of the desensitization occurring after 7.5 min of pretreatment. SKF 104353 (100 nM), a high affinity, LTD4-receptor antagonist, blocked completely LTD4-induced desensitization of RBL-1 cells. The LTD4-induced desensitization was stereospecific, as the (5R,6S)-enantiomer of LTD4 was at least 100 times less potent than LTD4. Pretreatment of RBL-1 cells with LTD4 did not alter the ability of thrombin or ATP to induce [Ca++]i mobilization, suggesting that the desensitization was of the "homologous" type. The density of [3H]LTD4 receptors in RBL-1 cell membranes was decreased 23% by prior treatment of RBL-1 cells with LTD4. These results demonstrate that the [Ca++]i mobilization induced by LTD4 can be desensitized as a result of prior exposure to LTD4 and that the LTD4 receptor and/or second messenger systems can be specifically down-regulated.

摘要

我们实验室之前的研究表明,RBL-1细胞表达白三烯(LT)D4的膜受体,这些受体的激动剂刺激会导致细胞内钙([Ca++]i)的动员。我们利用这一LTD4受体介导的事件来研究RBL-1细胞中的同源脱敏作用。将RBL-1细胞预先暴露于LTD4会导致最大[Ca++]i动员量减少40%。这种脱敏作用具有浓度和时间依赖性,EC50为1至3 nM,50%的脱敏作用在预处理7.5分钟后出现。高亲和力的LTD4受体拮抗剂SKF 104353(100 nM)可完全阻断LTD4诱导的RBL-1细胞脱敏。LTD4诱导的脱敏具有立体特异性,因为LTD4的(5R,6S)对映体的效力比LTD4至少低100倍。用LTD4预处理RBL-1细胞不会改变凝血酶或ATP诱导[Ca++]i动员的能力,这表明脱敏是“同源”类型的。用LTD4预先处理RBL-1细胞会使RBL-1细胞膜中[3H]LTD4受体的密度降低23%。这些结果表明,LTD4诱导的[Ca++]i动员可因预先暴露于LTD4而脱敏,并且LTD4受体和/或第二信使系统可被特异性下调。

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