Possible role for Ca2+ calmodulin-dependent protein kinase II as an effector of the fertilization Ca2+ signal in mouse oocyte activation

The present study shows that Ca2+ calmodulin-dependent protein kinase II (CaM kinase II) is physiologically activated in fertilized mouse oocytes and is involved in the Ca2+ response pathways that link the fertilization Ca2+ signal to meiosis resumption and cortical granule (CG) exocytosis. After 10 min of insemination, CaM kinase II activity increased transiently, then peaked at 1 h and remained elevated 30 min later when most of the oocytes had completed the emission of the second polar body. In contrast, in ethanol-activated oocytes the early transient activation of CaM kinase II in response to a monotonic Ca2+ rise was not followed by any subsequent increase. Inhibition of CaM kinase II by 20 mumol/l myristoylated-AIP (autocamtide-2-related inhibitory peptide) negatively affected MPF (maturing promoting factor) inactivation, cell cycle resumption and CG exocytosis in both fertilized and ethanol-activated oocytes. These results indicate that the activation of CaM kinase II in mouse oocytes is differently modulated by a monotonic or repetitive Ca2+ rise and that it is essential for triggering regular oocyte activation.