This may e plain partial but sta tistically significant inhibition of acrosome reaction by human SIZP in presence of Pertussis to in. One major component of signal transduction cascade downstream to Gi protein is adenylate cyclase that therefore gen erates second messenger cAMP upon its activation. cAMP in turn binds and activates protein kinase A in addition to other kinases. In humans, pharmacological inhibition of cAMP dependent PKA by KT5720 has been shown to reduce SIZP induced acrosome reaction. Native purified human ZP4 but not ZP3, mediated induction of acrosome reaction has been shown to be inhibited in capacitated human sperm following pre treatment with H 89, pharmacological inhibitor of PKA. Our findings with human SIZP which contain all four zona proteins showed a significant inhibition in induction of acrosome reaction in presence of H89.

thereby suggesting that human ZP mediated acro some reaction involves other zona proteins in addition to ZP4. Various other kinases are also involved in ZP mediated acrosome reaction either through direct or indirect activation of downstream effector molecules in the signalling cascade. An important role of protein kinase C in human ZP induced acrosome reaction has been suggested employing human oocytes, where PKC activator, Phorbol 12 myristate 13 acetate, showed enhanced human ZP induced acrosome reaction and PKC inhibitor, staurosporine, decreased e tent of acrosome reaction. In humans, SIZP induced acro some reaction has also been shown to be inhibited by PKC inhibitor, Calphostin.

Native purified human ZP3 and ZP4 mediated acrosome reaction also showed an inhibition in acrosome reaction following PKC inhi bitor, chelerythrine chloride pre treatment. Our find ings with solubilized zona also highlight the role of PKC in zona induced acrosome reaction. The importance of both PKA and PKC pathways is further emphasised dur ing fertilization by the observations of enhanced sperm ZP binding in presence of PKA and PKC activators. Recent studies in murine system implicate important role of PI 3 kinase in ZP induced acrosome reaction. Treatment of capacitated mouse sperm with ZP3 stimulates production of phosphatidylinositol tri phosphate and which in turn activates protein kinases, Akt and PKC��, which function as downstream effectors of phosphoinositide signalling.

Capacitated mouse sperm pre treated with two different pharmacological inhibitors of PI 3 kinase, Wortmannin or LY294002, before e posure to either a soluble e tract of zonae or with purified ZP3 resulted in 90% inhibition in acrosome reaction. In human sperm the rele vance AV-951 of PI 3 kinase has been demonstrated in man nose bovine serum albumin mediated acrosome selleck inhibitor reaction. Wortmannin was shown to inhibit the mannose BSA mediated acrosomal e ocytosis but not that induced by calcium ionophore, A23187 or by progesterone. In this manuscript, for the first time, we have shown the role of PI 3 kinase in human SIZP mediated acrosome reaction.