Protease expression in the human and rat cumulus-oocyte complex during the periovulatory period: a role in cumulus-oocyte complex migration†.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Ketan Shrestha, Muraly Puttabyatappa, Michelle A Wynn, Patrick R Hannon, Linah F Al-Alem, Katherine L Rosewell, James Akin, Thomas E Curry
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Abstract

The migratory and matrix-invading capacities of the cumulus-oocyte complex have been shown to be important for the ovulatory process. In metastatic cancers, these capacities are due to increased expression of proteases, however, there is limited information on protease expression in the cumulus-oocyte complexes. The present study examined cumulus-oocyte complex expression of plasmins, matrix metalloproteases, and A Disintegrin and Metalloproteinase with Thrombospondin Motifs family members in the rat and human. In the rat, human chorionic gonadotropin (hCG) administration increased cumulus-oocyte complex expression of Mmp2, Mmp9, Mmp13, Mmp14, Mmp16, Adamts1, and the protease inhibitors Timp1, Timp3, and Serpine1 by 8-12 h. This ovulatory induction of proteases in vivo could be mimicked by forskolin and ampiregulin treatment of cultured rat cumulus-oocyte complexes with increases observed in Mmp2, Mmp13, Mmp14, Mmp16, Mmp19, Plat, and the protease inhibitors Timp1, Timp3, and Serpine1. Comparison of expression between rat cumulus-oocyte complexes and granulosa cells at the time of ovulation showed decreased Mmp9 and increased Mmp13, Mmp14, Mmp16, Adamts1, Timp1, and Timp3 expression in the cumulus-oocyte complexes. In human, comparison of expression between cumulus and granulosa cells at the time of in vitro fertilization retrieval showed decreased MMP1, MMP2, MMP9, and ADAMTS1, while expression of MMP16, TIMP1, and TIMP3 were increased. Treatment of expanding rat cumulus-oocyte complexes with a broad spectrum matrix metalloproteases inhibitor, GM6001, significantly reduced the migration of cumulus cells in vitro. These data provide evidence that multiple proteases and their inhibitors are expressed in the cumulus-oocyte complex and play an important role in imparting the migratory phenotype of the cumulus-oocyte complex at the time of ovulation. Summary Sentence  Multiple proteases and their inhibitors are induced in the cumulus-oocyte complex (COC) during the periovulatory period and potentially play an important role in imparting the migratory phenotype of the COC at the time of ovulation.

围排卵期人和大鼠积层卵母细胞复合体(COC)中蛋白酶的表达:在 COC 迁移中的作用
事实证明,积卵母细胞复合体(COC)的迁移和基质侵入能力对排卵过程非常重要。在转移性癌症中,这些能力是由于蛋白酶表达的增加,然而,有关 COC 中蛋白酶表达的信息却很有限。本研究检测了大鼠和人类 COC 中血浆蛋白酶、基质金属蛋白酶(MMP)和具有凝血酶原软骨蛋白酶(ADAMTS)家族成员的表达情况。在大鼠体内,施用 hCG 会在 8-12 小时内增加 COC 中 Mmp2、Mmp9、Mmp13、Mmp14、Mmp16、Adamts1 以及蛋白酶抑制剂 Timp1、Timp3 和 Serpine1 的表达。体内蛋白酶的这种排卵诱导可通过对培养的大鼠 COC 进行福斯可林和安非他酮处理来模拟,并观察到 Mmp2、Mmp13、Mmp14、Mmp16、Mmp19、Plat 以及蛋白酶抑制剂 Timp1、Timp3 和 Serpine1 的增加。比较大鼠 COC 和颗粒细胞在排卵时的表达,发现 COC 中 Mmp9 表达减少,Mmp13、Mmp14、Mmp16、Adamts1、Timp1 和 Timp3 表达增加。对人类试管婴儿取卵时的积层细胞和颗粒细胞的表达进行比较后发现,MMP1、MMP2、MMP9 和 ADAMTS1 的表达减少,而 MMP16、TIMP1 和 TIMP3 的表达增加。用广谱 MMP 抑制剂 GM6001 处理扩增的大鼠 COC,可显著减少积层细胞在体外的迁移。这些数据提供了证据,证明多种蛋白酶及其抑制剂在 COC 中表达,并在排卵时赋予 COC 迁移表型方面发挥重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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