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蛋白激酶C抑制剂可阻止脂多糖刺激的小鼠B细胞由白细胞介素-5诱导的IgA合成。

IL-5-induced IgA synthesis by LPS-stimulated mouse B cells is prevented by protein kinase C inhibitors.

作者信息

Li Y S, Gimond C, Revillard J P

机构信息

Laboratory of Immunology, INSERM U. 80, CNRS URA 1177, UCBL, Hôpital E. Herriot, Lyon, France.

出版信息

Eur Cytokine Netw. 1992 Mar-Apr;3(2):103-7.

PMID:1586701
Abstract

We have previously demonstrated that activation of protein kinase C (PKC) by phorbol esters induces selectively IgA synthesis by mouse B cells. In this study, we investigated the effects of a number of protein kinase inhibitors on IgA secretion induced by a recombinant murine IL-5 in LPS-stimulated mouse B cells. The results show that PKC inhibitors, such as sphingosine (SPH), staurosporine (STP) and H-7, blocked IL-5-induced IgA synthesis; the protein kinase A inhibitor HA-1004 and the inhibitor of calcium/calmodulin dependent protein kinase W-7 had no effect on IgA secretion induced by IL-5. The proliferation of the IL-5 sensitive B13 cell line in response to IL-5 was also inhibited by addition of SPH or STP or H-7. The data suggest an involvement of the PKC pathway in IL-5-induced B cell differentiation into IgA secreting cells.

摘要

我们先前已经证明,佛波酯激活蛋白激酶C(PKC)可选择性地诱导小鼠B细胞合成IgA。在本研究中,我们研究了多种蛋白激酶抑制剂对重组鼠IL-5在LPS刺激的小鼠B细胞中诱导的IgA分泌的影响。结果表明,PKC抑制剂,如鞘氨醇(SPH)、星形孢菌素(STP)和H-7,可阻断IL-5诱导的IgA合成;蛋白激酶A抑制剂HA-1004和钙/钙调蛋白依赖性蛋白激酶抑制剂W-7对IL-5诱导的IgA分泌没有影响。添加SPH、STP或H-7也可抑制IL-敏感受性B13细胞系对IL-5的增殖反应。数据表明PKC途径参与了IL-5诱导的B细胞分化为IgA分泌细胞的过程。

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