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固定化透明带基质诱导兔精子顶体反应过程中顶体蛋白酶的定位

Localization of rabbit sperm acrosin during the acrosome reaction induced by immobilized zona matrix.

作者信息

Richardson R T, Nikolajczyk B S, Abdullah L H, Beavers J C, O'Rand M G

机构信息

Department of Cell Biology and Anatomy, University of North Carolina, Chapel Hill 27599.

出版信息

Biol Reprod. 1991 Jul;45(1):20-6. doi: 10.1095/biolreprod45.1.20.

Abstract

To better understand the loss of the acrosomal cap on the surface of the zona pellucida and the function of the equatorial-postacrosomal region after the acrosome reaction, we have constructed an in vitro system using heat-solubilized zonae pellucidae dried onto a coverslip and incubated with capacitated spermatozoa. This system allows good optical resolution of spermatozoonzona interaction. Induction of the acrosome reaction by zonae on coverslips (30%) is comparable to the induction of the reaction reported previously for rabbit spermatozoa using solubilized zonae in solution. Antiserum to rabbit proacrosin, antiserum to a porcine 49-kDa proacrosin fragment, and antiserum to a porcine 14-kDa C-terminal acrosin fragment were utilized to monitor the acrosome reaction. Rabbit proacrosin/acrosin is not present on the surface of live, acrosome-intact, swimming spermatozoa. After contact with zona, the acrosome reaction begins and proacrosin/acrosin becomes available to bind antibody, first as a crescent in the apical region and then more posteriorly until the entire anterior acrosome is labeled. Proacrosin/acrosin remains on the equatorial and postacrosomal regions of acrosome-reacted spermatozoa and also remains associated with the acrosomal cap even after the spermatozoon is no longer associated with it. Further studies using zona-coated coverslips should lead to a more detailed understanding of the mechanism of zona penetration.

摘要

为了更好地理解透明带上顶体帽的丢失以及顶体反应后赤道后顶体区域的功能,我们构建了一个体外系统,该系统使用热溶解的透明带干燥在盖玻片上,并与获能精子一起孵育。这个系统能够很好地观察精子与透明带相互作用的光学分辨率。盖玻片上的透明带诱导顶体反应(30%)与先前报道的使用溶液中溶解的透明带诱导兔精子顶体反应的情况相当。使用抗兔前顶体蛋白酶抗血清、抗猪49 kDa前顶体蛋白酶片段抗血清和抗猪14 kDa C末端顶体蛋白酶片段抗血清来监测顶体反应。兔前顶体蛋白酶/顶体蛋白酶不存在于活的、顶体完整、游动的精子表面。与透明带接触后,顶体反应开始,前顶体蛋白酶/顶体蛋白酶变得可与抗体结合,首先在顶端区域呈新月形,然后更靠后,直到整个顶体前部被标记。前顶体蛋白酶/顶体蛋白酶保留在顶体反应精子的赤道和后顶体区域,并且即使精子不再与之相关联,也仍然与顶体帽相关。使用包被透明带的盖玻片进行的进一步研究应该会导致对透明带穿透机制有更详细的了解。

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