Phospholipase C in mouse oocytes: Characterization of beta and gamma isoforms and their possible involvement in sperm-induced Ca2+ spiking

被引:124
作者
Dupont, G
McGuinness, OM
Johnson, MH
Berridge, MJ
Borgese, F
机构
[1] UNIV CAMBRIDGE, DEPT ZOOL, BABRAHAM INST MOLEC SIGNALLING, CAMBRIDGE CB2 3EJ, ENGLAND
[2] FREE UNIV BRUSSELS, FAC SCI CP231, B-1050 BRUSSELS, BELGIUM
[3] UNIV CAMBRIDGE, DEPT ANAT, CAMBRIDGE CB2 3DY, ENGLAND
[4] CEA, URA 1855 CNRS, LAB JEAN MAETZ, F-06230 VILLEFRANCHE SUR MER, FRANCE
关键词
D O I
10.1042/bj3160583
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
This study involved an investigation of the role of phospholipase C (PLC) in generating repetitive Ca2+ spikes at fertilization. Using a PCR-based strategy we have demonstrated that mouse oocytes have mRNA coding for PLC beta 1, PLC beta 3 and PLC gamma isoenzymes. Furthermore, immunodetection of PLC gamma 1 using monoclonal antibodies reveals that PLC gamma 1 protein is present in mature mouse oocytes, ruling out the possibility that mRNA was being transcribed but not expressed. We were unsuccessful at detecting the presence of PLC beta protein, but the presence of this isoform can be inferred from functional studies. The PLC inhibitor, U73122, exerted an inhibitory effect on oocytes activated by spermatozoa or acetylcholine at concentrations of 10 and 30 mu M respectively, while its inactive analogue had no effect. The soluble tyrosine kinase inhibitors, genistein (100 mu M), herbimycin (10 mu M) and geldanamycin (0.6 mu M) which could affect signalling through PLC gamma hindered but never completely inhibited Ca2+ spiking in response to fertilization. We conclude that the activation of PLC to generate InsP(3) may play a critical role in fertilization.
引用
收藏
页码:583 / 591
页数:9
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