State Key Laboratory of Medical Genomics, Research Center for Experimental Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Biol Reprod. 2022 Oct 11;107(4):1139-1154. doi: 10.1093/biolre/ioac146.
Serine proteases (PRSS) constitute nearly one-third of all proteases, and many of them have been identified to be testis-specific and play significant roles during sperm development and male reproduction. PRSS54 is one of the testis-specific PRSS in mouse and human but its physiological function remains largely unclear. In the present study, we demonstrate in detail that PRSS54 exists not only in testis but also in mature sperm, exhibiting a change in protein size from 50 kDa in testis to 42 kDa in sperm. Loss of PRSS54 in mice results in male subfertility, acrosome deformation, defective sperm-zona penetration, and phenotypes of male subfertility and acrosome deformation can be rescued by Prss54 transgene. Ultrastructure analyses by transmission electronic microscopy further reveal various morphological abnormalities of Prss54-/- spermatids during spermiogenesis, including unfused vacuoles in acrosome, detachment and eccentrical localization of the acrosomal granules, and asymmetrical elongation of the nucleus. Subcellular localization of PRSS54 display that it appears in the acrosomal granule at the early phase of acrosome biogenesis, then extends along the inner acrosomal membrane, and ultimately presents in the acrosome region of the mature sperm. PRSS54 interacts with acrosomal proteins ZPBP1, ZPBP2, ACRBP, and ZP3R, and loss of PRSS54 affects the distribution of these proteins in testis and sperm, although their protein levels are largely unaffected. Moreover, Prss54-/- sperm are more sensitive to acrosome reaction inducers.
丝氨酸蛋白酶(PRSS)构成了所有蛋白酶的近三分之一,其中许多已被鉴定为睾丸特异性,在精子发生和男性生殖中发挥重要作用。PRSS54 是小鼠和人类中一种睾丸特异性 PRSS,但它的生理功能仍很大程度上不清楚。在本研究中,我们详细证明 PRSS54 不仅存在于睾丸中,也存在于成熟精子中,其蛋白大小从睾丸中的 50 kDa 变为精子中的 42 kDa。PRSS54 在小鼠中的缺失导致雄性生育力下降、顶体变形、精子-透明带穿透缺陷,并且 Prss54 转基因可挽救雄性生育力下降和顶体变形表型。透射电子显微镜的超微结构分析进一步揭示了 Prss54-/-精母细胞在精子发生过程中各种形态异常,包括顶体中未融合的空泡、顶体颗粒的分离和偏心定位以及核的不对称伸长。PRSS54 的亚细胞定位显示,它在顶体发生的早期出现在顶体颗粒中,然后沿着内顶体膜延伸,最终出现在成熟精子的顶体区域。PRSS54 与顶体蛋白 ZPBP1、ZPBP2、ACRBP 和 ZP3R 相互作用,PRSS54 的缺失影响这些蛋白在睾丸和精子中的分布,尽管它们的蛋白水平在很大程度上没有受到影响。此外,Prss54-/-精子对顶体反应诱导剂更敏感。