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佛波酯抑制小鼠B细胞分化为免疫球蛋白分泌细胞,但不抑制其增殖。

Phorbol esters inhibit murine B cell differentiation to immunoglobulin secretion but not proliferation.

作者信息

Isakson P C, Simpson L

出版信息

J Immunol. 1984 Oct;133(4):1788-91.

PMID:6332133
Abstract

Bacterial lipopolysaccharide (LPS) induces resting B cells to proliferate and to secrete IgM. We have found that addition of phorbol esters (PE) such as phorbol myristate acetate (PMA) to murine B cells specifically inhibits LPS-induced IgM secretion but not proliferation. PMA is extremely potent, with half-maximal inhibition occurring at about 10 pM. The effect on B cells appears to be due to interaction with PE receptors, because a series of PE have similar potencies for tumor promotion, binding to receptors, and inhibition of IgM secretion. PE also inhibit IgM secretion induced by T cell-derived lymphokines and LPS-induced IgG secretion. Results of these studies suggest that the protein kinase C, with which PE interact, plays an important role in the regulation of B cell differentiation and may also provide a powerful tool for dissecting molecular events involved in induction of Ig secretion.

摘要

细菌脂多糖(LPS)可诱导静止的B细胞增殖并分泌IgM。我们发现,向鼠B细胞中添加佛波酯(PE),如佛波醇肉豆蔻酸酯乙酸酯(PMA),可特异性抑制LPS诱导的IgM分泌,但不抑制增殖。PMA的作用极强,半数最大抑制浓度约为10 pM。对B细胞的作用似乎是由于与PE受体相互作用,因为一系列PE在肿瘤促进、与受体结合以及抑制IgM分泌方面具有相似的效力。PE还可抑制T细胞衍生的淋巴因子诱导的IgM分泌以及LPS诱导的IgG分泌。这些研究结果表明,与PE相互作用的蛋白激酶C在B细胞分化调节中起重要作用,并且可能还为剖析参与Ig分泌诱导的分子事件提供了一个有力工具。

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