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大鼠肥大细胞系中肿瘤坏死因子的分泌是一个对布雷菲德菌素A敏感且受钙/蛋白激酶C调节的过程。

Secretion of TNF from a rat mast cell line is a brefeldin A-sensitive and a calcium/protein kinase C-regulated process.

作者信息

Baumgartner R A, Yamada K, Deramo V A, Beaven M A

机构信息

Laboratory of Chemical Pharmacology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892.

出版信息

J Immunol. 1994 Sep 15;153(6):2609-17.

PMID:8077671
Abstract

Stimulated mast cells and cognate cultured cell lines produce and secrete a variety of cytokines including TNF. Because the mechanism by which cytokines are delivered to the external milieu is unknown, the release of TNF was studied in a rat mast cell line (RBL-2H3 cells). In these cells, TNF was not constitutively expressed nor incorporated into secretory granules but was generated de novo upon cell stimulation. It was then released by a process analogous to constitutive secretion in that brefeldin A, an agent known to disrupt Golgi membranes in these cells, inhibited this release without inhibiting release of secretory granules. Unlike constitutive secretion, however, the secretion of TNF was highly regulated by Ca2+ and protein kinase C. Studies with various stimulants and inhibitors indicated that simultaneous mobilization of Ca2+ and activation of protein kinase C were sufficient signals for secretion although optimal production of TNF may be dependent on additional synergistic signals. Because suppression of Ca2+ mobilization or inhibition of protein kinase C alone abrogated TNF secretion, the process may be amenable to therapeutic intervention.

摘要

受到刺激的肥大细胞和相关培养细胞系会产生并分泌包括肿瘤坏死因子(TNF)在内的多种细胞因子。由于细胞因子释放到细胞外环境的机制尚不清楚,因此在大鼠肥大细胞系(RBL-2H3细胞)中研究了TNF的释放。在这些细胞中,TNF不是组成性表达的,也不会整合到分泌颗粒中,而是在细胞受到刺激时重新产生。然后,它通过类似于组成性分泌的过程释放,因为布雷菲德菌素A(一种已知会破坏这些细胞中高尔基体膜的试剂)会抑制这种释放,而不会抑制分泌颗粒的释放。然而,与组成性分泌不同,TNF的分泌受到Ca2+和蛋白激酶C的高度调节。对各种刺激剂和抑制剂的研究表明,Ca2+的同时动员和蛋白激酶C的激活是分泌的充分信号,尽管TNF的最佳产生可能依赖于其他协同信号。由于单独抑制Ca2+的动员或抑制蛋白激酶C会消除TNF的分泌,因此该过程可能适合进行治疗干预。

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