Reduced amounts and abnormal forms of phospholipase C zeta (PLC ) in spermatozoa from infertile men

Elke Heytens(Ghent University Hospital), John Parrington(University of Oxford), Kevin Coward(John Radcliffe Hospital), Claire Young(University of Oxford), Stijn Lambrecht(Ghent University), Sook Young Yoon(University of Massachusetts Amherst), Rafael A. Fissore(University of Massachusetts Amherst), Rebecca Hamer(Ghent University), Charlotte M. Deane(University of Oxford), Margarida Ruas(University of Oxford), Patricia Grasa(University of Oxford), Reza Soleimani(Ghent University Hospital), Claude Cuvelier(Ghent University Hospital), Jan Gerris(Ghent University Hospital), Marc Dhont(Ghent University Hospital), Dieter Deforce(Ghent University), Luc Leybaert(Ghent University), Petra De Sutter(Ghent University Hospital)
Human Reproduction
July 7, 2009
Cited by 293Open Access
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Abstract

BACKGROUND: In mammals, oocyte activation at fertilization is thought to be induced by the sperm-specific phospholipase C zeta (PLCzeta). However, it still remains to be conclusively shown that PLCzeta is the endogenous agent of oocyte activation. Some types of human infertility appear to be caused by failure of the sperm to activate and this may be due to specific defects in PLCzeta. METHODS AND RESULTS: Immunofluorescence studies showed PLCzeta to be localized in the equatorial region of sperm from fertile men, but sperm deficient in oocyte activation exhibited no specific signal in this same region. Immunoblot analysis revealed reduced amounts of PLCzeta in sperm from infertile men, and in some cases, the presence of an abnormally low molecular weight form of PLCzeta. In one non-globozoospermic case, DNA analysis identified a point mutation in the PLCzeta gene that leads to a significant amino acid change in the catalytic region of the protein. Structural modelling suggested that this defect may have important effects upon the structure and function of the PLCzeta protein. cRNA corresponding to mutant PLCzeta failed to induce calcium oscillations when microinjected into mouse oocytes. Injection of infertile human sperm into mouse oocytes failed to activate the oocyte or trigger calcium oscillations. Injection of such infertile sperm followed by two calcium pulses, induced by assisted oocyte activation, activated the oocytes without inducing the typical pattern of calcium oscillations. CONCLUSIONS: Our findings illustrate the importance of PLCzeta during fertilization and suggest that mutant forms of PLCzeta may underlie certain types of human male infertility.


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