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精子蛋白酶体在精子星体形成和早期合子发育中的作用:对人类受精失败的启示

The role of sperm proteasomes during sperm aster formation and early zygote development: implications for fertilization failure in humans.

作者信息

Rawe Vanesa Y, Díaz Emilce S, Abdelmassih Roger, Wójcik Cezary, Morales Patricio, Sutovsky Peter, Chemes Héctor E

机构信息

Centro de Estudios en Ginecología y Reproducción (CEGyR), Buenos Aires, Argentina.

出版信息

Hum Reprod. 2008 Mar;23(3):573-80. doi: 10.1093/humrep/dem385. Epub 2007 Dec 17.

DOI:10.1093/humrep/dem385
PMID:18089554
Abstract

BACKGROUND Sperm aster organization during bovine and human fertilization requires a paternally-derived centriole that must first disengage from the sperm tail connecting-piece. We investigated the participation of the 26S proteasome in this process. METHODS Proteasome localization and enzymatic activity were studied in normal and pathological human spermatozoa by immunocytochemistry and enzyme-substrate assays. The role of proteasomes during bovine zygote development was investigated using a pharmacological proteasome-inhibitor, MG132, and with anti-proteasome antibodies delivered by Streptolysin O-permeabilization or with the Chariot reagent. Human zygotes discarded after ICSI failures (n = 28) were also examined. RESULTS Proteasomes were localized in the sperm acrosome and connecting-piece, as well as in the pronuclei of bovine and human zygotes. Proteasomal enzymatic activities were decreased in defective human spermatozoa. Disrupted sperm aster formation and pronuclear development were found after pharmacological and immunological block of proteasomes in human/bovine spermatozoa and oocytes, as well as in 28 discarded human post-ICSI fertilization failures. CONCLUSIONS Specific proteasome inhibition disrupts sperm aster formation and pronuclear development/apposition in bovine and human zygotes. Human spermatozoa with defective centriolar/pericentriolar structures have decreased proteasomal enzymatic activity. Release of a functional sperm centriole that acts as a zygote microtubule-organizing center probably relies on selective proteasomal proteolysis. These findings suggest an important role of sperm proteasomes in zygotic development.

摘要

背景 在牛和人类受精过程中,精子星体的形成需要一个来自父方的中心粒,该中心粒必须首先从精子尾部连接段脱离。我们研究了26S蛋白酶体在这一过程中的作用。

方法 通过免疫细胞化学和酶-底物分析,研究正常和病理状态下人类精子中蛋白酶体的定位和酶活性。使用蛋白酶体抑制剂MG132、通过链球菌溶血素O通透法或用Chariot试剂递送的抗蛋白酶体抗体,研究蛋白酶体在牛合子发育过程中的作用。还对ICSI失败后丢弃的人类合子(n = 28)进行了检查。

结果 蛋白酶体定位于精子顶体和连接段,以及牛和人类合子的原核中。在有缺陷的人类精子中,蛋白酶体酶活性降低。在对人类/牛精子和卵母细胞进行蛋白酶体的药理学和免疫学阻断后,以及在28例丢弃的人类ICSI后受精失败病例中,发现精子星体形成和原核发育受到破坏。

结论 特异性蛋白酶体抑制会破坏牛和人类合子中的精子星体形成以及原核发育/并置。具有中心粒/中心粒周围结构缺陷的人类精子,其蛋白酶体酶活性降低。释放一个作为合子微管组织中心的功能性精子中心粒,可能依赖于选择性蛋白酶体蛋白水解作用。这些发现表明精子蛋白酶体在合子发育中起重要作用。

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