Kouchi Zen, Fukami Kiyoko, Shikano Tomohide, Oda Shoji, Nakamura Yoshikazu, Takenawa Tadaomi, Miyazaki Shunichi
Department of Physiology, Tokyo Women's Medical University School of Medicine, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, Japan.
J Biol Chem. 2004 Mar 12;279(11):10408-12. doi: 10.1074/jbc.M313801200. Epub 2003 Dec 29.
Sperm-specific phospholipase Czeta (PLCzeta) is known to induce intracellular Ca(2+) oscillations and subsequent early embryonic development when expressed in mouse eggs by injection of RNA encoding PLCzeta (Saunders, C. M., Larman, M. G., Parrington, J., Cox, L. J., Royse, J., Blayney, L. M., Swann, K., and Lai, F. A. (2002) Development 129, 3533-3544). The present study addressed characteristics of purified mouse PLCzeta protein that was synthesized using the baculovirus/Sf9 cell expression system. Microinjection of recombinant PLCzeta protein into mouse eggs induced serial Ca(2+) spikes quite similar to those produced by the injection of sperm extract, probably because of repetitive Ca(2+) release from the endoplasmic reticulum caused by continuously produced inositol 1,4,5-trisphosphate. Recombinant PLCdelta1 also induced Ca(2+) oscillations, but a 20-fold higher concentration was required compared with PLCzeta. In the enzymatic assay of phosphatidylinositol 4,5-bisphosphate hydrolyzing activity in vitro at various calcium ion concentrations ([Ca(2+)]), PLCzeta exhibited a significant activity at [Ca(2+)] as low as 10 nm and had 70% maximal activity at 100 nm [Ca(2+)] that is usually the basal intracellular calcium ion concentration level of cells. On the other hand, the activity of PLCdelta1 increased at a [Ca(2+)] between 1 and 30 microm. EC(50) was 52 nm for PLCzeta and 5.7 microm for PLCdelta1. Thus, PLCzeta has an approximately 100-fold higher Ca(2+) sensitivity than PLCdelta1. The ability of purified PLCzeta protein to induce Ca(2+) oscillations qualifies PLCzeta as a proper candidate of the mammalian egg-activating sperm factor. Furthermore, such a high Ca(2+) sensitivity of PLC activity as PLCzeta that can be active in cells at the resting state is thought to be an appropriate characteristic of the sperm factor, which is introduced into the ooplasm upon sperm-egg fusion, triggers Ca(2+) release first, and maintains Ca(2+) oscillations.
已知精子特异性磷脂酶Cζ(PLCζ)在通过注射编码PLCζ的RNA而在小鼠卵中表达时,会诱导细胞内Ca(2+)振荡及随后的早期胚胎发育(桑德斯,C.M.,拉曼,M.G.,帕林顿,J.,考克斯,L.J.,罗伊斯,J.,布莱尼,L.M.,斯旺,K.,以及赖,F.A.(2002年)《发育》129卷,3533 - 3544页)。本研究探讨了使用杆状病毒/Sf9细胞表达系统合成的纯化小鼠PLCζ蛋白的特性。将重组PLCζ蛋白显微注射到小鼠卵中会诱导出一系列Ca(2+)尖峰,与注射精子提取物所产生的尖峰非常相似,这可能是由于持续产生的肌醇1,4,5 - 三磷酸导致内质网中Ca(2+)的重复释放。重组PLCδ1也能诱导Ca(2+)振荡,但与PLCζ相比需要高20倍的浓度。在不同钙离子浓度([Ca(2+)])下对磷脂酰肌醇4,5 - 二磷酸水解活性进行体外酶活性测定时,PLCζ在低至10纳米的[Ca(2+)]时就表现出显著活性,在100纳米[Ca(2+)]时具有70%的最大活性,而100纳米[Ca(2+)]通常是细胞内钙离子浓度的基础水平。另一方面,PLCδ1的活性在[Ca(2+)]为1至30微摩尔之间时增加。PLCζ的半数有效浓度(EC(50))为52纳米,PLCδ1的为5.7微摩尔。因此,PLCζ对Ca(2+)的敏感性比PLCδ1高约100倍。纯化的PLCζ蛋白诱导Ca(2+)振荡的能力使PLCζ成为哺乳动物卵激活精子因子的合适候选者。此外,像PLCζ这样在静息状态下的细胞中就能具有活性的对Ca(2+)敏感性如此之高的PLC活性,被认为是精子因子的一个合适特性,该精子因子在精卵融合时被引入卵质,首先触发Ca(2+)释放,并维持Ca(2+)振荡。