Atypical isoforms of PKC and insulin secretion from pancreatic beta-cells: Evidence using Go 6976 and Ro 31-8220 as PKC inhibitors

被引:47
作者
Harris, TE
Persaud, SJ
Jones, PM
机构
[1] Cell./Molecular Endocrinology Group, Biomedical Sciences Division, King's College London, London W8 7AH, Campden Hill Road
基金
英国惠康基金;
关键词
D O I
10.1006/bbrc.1996.1567
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The involvement of protein kinase C (PKC) isoforms in glucose-induced insulin secretion was investigated by comparing the effects of the PKC inhibitors Go 6976, which is PKC-specific and selective for the Ca2+-dependent isoforms, and Ro 31-8220, a specific PKC inhibitor which does not discriminate between isoforms. G6 6976 inhibited the Ca2+- and diacylglycerol (DAG)-dependent PKC activities in beta-cell extracts in vitro and fully inhibited insulin secretory responses of rat islets of Langerhans to the PKC activator 4 beta phorbol myristate acetate (PMA), suggesting that it was an effective inhibitor of the DAG-dependent isoforms of PKC in situ. However. glucose-induced insulin secretion from rat islets was not inhibited by Go 6976, whereas secretory responses to glucose were partially inhibited by the non-isoform selective PKC inhibitor, Ro 31-8220. The simplest explanation of these results is that glucose-induced insulin secretion is dependent, at least in part, upon the activation of an atypical isoform(s) of PKC within the beta-cell. (C) 1996 Academic Press, Inc.
引用
收藏
页码:672 / 676
页数:5
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