Saleh Alaaeldin, Kashir Junaid, Thanassoulas Angelos, Safieh-Garabedian Bared, Lai F Anthony, Nomikos Michail
Member of QU Health, College of Medicine, Qatar University, Doha, Qatar.
College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
Front Cell Dev Biol. 2020 Jan 29;8:28. doi: 10.3389/fcell.2020.00028. eCollection 2020.
Sperm-specific phospholipase C zeta (PLCζ) is widely considered to be the physiological stimulus responsible for generating calcium (Ca) oscillations that induce egg activation and early embryonic development during mammalian fertilization. In the mammalian testis, PLCζ expression is detected at spermiogenesis following elongated spermatid differentiation. Sperm-delivered PLCζ induces Ca release via the inositol 1,4,5-trisphosphate (InsP) signaling pathway. PLCζ is the smallest known mammalian PLC isoform identified to date, with the simplest domain organization. However, the distinctive biochemical properties of PLCζ compared with other PLC isoforms contribute to its unique potency in stimulating cytosolic Ca oscillations within mammalian eggs. Moreover, studies describing PLCζ "knockout" mouse phenotypes confirm the supreme importance of PLCζ at egg activation and monospermic fertilization in mice. Importantly, a number of clinical reports have highlighted the crucial importance of PLCζ in human fertilization by associating PLCζ deficiencies with certain forms of male factor infertility. Herein, we give an update on recent advances that have refined our understanding of how sperm PLCζ triggers Ca oscillations and egg activation in mammals, while also discussing the nature of a potential "alternative" sperm factor. We summarise PLCζ localization in mammalian sperm, and the direct links observed between defective PLCζ protein in sperm and documented cases of male infertility. Finally, we postulate how this sperm protein can be used as a potential diagnostic marker, and also as a powerful therapeutic agent for treatment of certain types of male infertility due to egg activation failure or even in more general cases of male subfertility.
精子特异性磷脂酶Cζ(PLCζ)被广泛认为是在哺乳动物受精过程中产生钙(Ca)振荡的生理刺激物,该振荡可诱导卵子激活和早期胚胎发育。在哺乳动物睾丸中,在延长的精子细胞分化后的精子发生过程中可检测到PLCζ的表达。精子传递的PLCζ通过肌醇1,4,5-三磷酸(InsP)信号通路诱导钙释放。PLCζ是迄今为止已知的最小的哺乳动物PLC亚型,其结构域组织最简单。然而,与其他PLC亚型相比,PLCζ独特的生化特性使其在刺激哺乳动物卵子胞质钙振荡方面具有独特的效力。此外,描述PLCζ“敲除”小鼠表型的研究证实了PLCζ在小鼠卵子激活和单精子受精中的至关重要性。重要的是,一些临床报告通过将PLCζ缺陷与某些形式的男性因素不孕症相关联,突出了PLCζ在人类受精中的关键重要性。在此,我们介绍了最近的进展,这些进展完善了我们对精子PLCζ如何触发哺乳动物钙振荡和卵子激活的理解,同时也讨论了潜在“替代”精子因子的性质。我们总结了PLCζ在哺乳动物精子中的定位,以及在精子中PLCζ蛋白缺陷与记录在案的男性不育病例之间观察到的直接联系。最后,我们推测这种精子蛋白如何能够用作潜在的诊断标志物,以及作为治疗某些类型因卵子激活失败导致的男性不育甚至更普遍的男性生育力低下病例的有力治疗剂。