The role of protein kinase C isozymes in bombesin-stimulated gastrin release from human antral gastrin cells

被引:14
作者
Moore, EDW [1 ]
Ring, M [1 ]
Scriven, DRL [1 ]
Smith, VC [1 ]
Meloche, RM [1 ]
Buchan, AMJ [1 ]
机构
[1] Univ British Columbia, Dept Physiol, Vancouver, BC V6T 1Z3, Canada
关键词
D O I
10.1074/jbc.274.32.22493
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
Two of the most effective stimuli of gastrin release from human antral G cells are bombesin and phorbol esters, Both agonists result in activation of the protein kinase C family of isozymes, however, the exact contribution of protein kinase C to the resultant release of gastrin has been difficult to assess, possibly due to the presence of multiple protein kinase C isozymes in the G cells. The results of the present study demonstrated that the human antral G cells expressed 6 protein kinase C isozymes alpha, gamma, theta, epsilon, zeta, and mu. Of these protein kinase C, gamma and theta were translocated by stimulation of the cells by either 10 nM bombesin or 1 mu M phorbol ester. Inhibition of protein kinase C mu (localized to the Golgi complex) did not decrease bombesin-stimulated gastrin release indicating that this isozyme was not involved in the secretory process. The use of selective antagonists of the calcium-sensitive conventional protein kinase C subgroup resulted in an increase in bombesin-stimulated gastrin release and indicated that protein kinase C gamma was involved in the desensitization of the bombesin response.
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收藏
页码:22493 / 22501
页数:9
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