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过氧化物酶 2 参与小鼠卵丘扩展和卵母细胞成熟。

Involvement of peroxiredoxin 2 in cumulus expansion and oocyte maturation in mice.

机构信息

Animal Facility of Aging Science, Korea Basic Science Institute, Gwangju 61186, Republic of Korea.

School of Biological Sciences and Biotechnology, Faculty of Life Science, Chonnam National University, Gwangju 61186, Republic of Korea.

出版信息

Reprod Fertil Dev. 2020 May;32(8):783-791. doi: 10.1071/RD19310.

Abstract

Peroxiredoxin 2 (Prdx2), an antioxidant enzyme, is expressed in the ovary during the ovulatory process. The aim of the present study was to examine the physiological role of Prdx2 during ovulation using Prdx2-knockout mice and mouse cumulus-oocyte complex (COC) from WT mice. Two days of treatment of immature mice (21-23 days old) with equine chorionic gonadotrophin and followed by treatment with human chorionic gonadotrophin greatly impaired cumulus expansion and oocyte maturation in Prdx2-knockout but not wild-type mice. Treatment of COCs in culture with conoidin A (50µM), a 2-cys Prdx inhibitor, abolished epiregulin (EPI)-induced cumulus expansion. Conoidin A treatment also inhibited EPI-stimulated signal molecules, including signal transducer and activator of transcription-3, AKT and mitogen-activated protein kinase 1/2. Conoidin A treatment also reduced the gene expression of EPI-stimulated expansion-inducing factors (hyaluronan synthase 2 (Has2), pentraxin 3 (Ptx3), TNF-α induced protein 6 (Tnfaip6) and prostaglandin-endoperoxide synthase 2 (Ptgs2)) and oocyte-derived factors (growth differentiation factor 9 (Gdf9) and bone morphogenetic protein 15 (Bmp15)). Furthermore, conoidin A inhibited EPI-induced oocyte maturation and the activity of connexins 43 and 37. Together, these results demonstrate that Prdx2 plays a role in regulating cumulus expansion and oocyte maturation during the ovulatory process in mice, probably by modulating epidermal growth factor receptor signalling.

摘要

过氧化物酶 2(Prdx2)是一种抗氧化酶,在排卵过程中在卵巢中表达。本研究旨在使用 Prdx2 敲除小鼠和来自 WT 小鼠的卵丘-卵母细胞复合物(COC)来研究 Prdx2 在排卵过程中的生理作用。用马绒毛膜促性腺激素处理 21-23 天大的未成熟小鼠 2 天,然后用人绒毛膜促性腺激素处理,极大地损害了 Prdx2 敲除但不是野生型小鼠的卵丘扩展和卵母细胞成熟。在培养中用 2-cys Prdx 抑制剂 conoidin A(50µM)处理 COC 会消除表皮生长因子诱导的卵丘扩展。Conoidin A 处理还抑制了 EPI 刺激的信号分子,包括信号转导和转录激活因子 3(STAT3)、AKT 和丝裂原激活蛋白激酶 1/2。Conoidin A 处理还降低了 EPI 刺激的扩展诱导因子(透明质酸合酶 2(Has2)、五聚素 3(Ptx3)、肿瘤坏死因子-α诱导蛋白 6(Tnfaip6)和前列腺素内过氧化物合酶 2(Ptgs2))和卵母细胞衍生因子(生长分化因子 9(Gdf9)和骨形态发生蛋白 15(Bmp15))的基因表达。此外,conoidin A 抑制了 EPI 诱导的卵母细胞成熟和连接蛋白 43 和 37 的活性。总之,这些结果表明 Prdx2 在调节小鼠排卵过程中的卵丘扩展和卵母细胞成熟中起作用,可能通过调节表皮生长因子受体信号。

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