热中性或热休克条件下体外成熟过程中抑制热休克蛋白90会影响牛卵母细胞的发育能力。

Zygote (Cambridge, England) Pub Date : 2022-12-01 Epub Date: 2022-09-15 DOI:10.1017/S0967199422000387
Eliza Diniz de Souza, Jessica Fernanda da Silva E Souza, Pedro Manoel de Oliveira Netto, Luciano de Rezende Carvalheira, Ribrio Ivan Tavares Pereira Batista, Carolina Capobiango Romano Quintão, Iuri Drumond Louro, Luiz Sergio Almeida Camargo
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引用次数: 0

摘要

热休克蛋白90 (Hsp90)对细胞稳态至关重要,但其在牛卵母细胞成熟过程中的作用尚不清楚。我们利用Hsp90抑制剂17-(烯丙胺)-17-demethoxygeldanamycin (17AAG)研究了Hsp90在体外成熟(IVM)过程中对牛卵母细胞能力的重要性。三个实验评估了17AAG对体外热中性(38.5℃)和热休克(HS;41.5ºC)温度。第一个实验发现,添加2µM 17AAG的小鼠囊胚率低于未添加0µM的对照组(P < 0.05)。17AAG浓度为2µM时,成熟卵母细胞HSF1转录本的丰度高于浓度为0和1µM时,而HSP90AA1和HSPA1A转录本的丰度低于浓度为0µM时(P < 0.05)。2µM 17AAG在IVM中作用12 h和24 h可降低囊胚率(P < 0.05)。在第三个实验中,IVM期间,2 μM 17AAG与HS关联12 h,囊胚率低于17AAG、HS和未处理的对照组(P < 0.05)。总之,在体外成熟过程中抑制Hsp90会影响胚胎的进一步发育;Hsp90抑制与HS的关联加重了两者对卵母细胞发育能力的有害影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of Hsp90 during in vitro maturation under thermoneutral or heat shock conditions compromises the developmental competence of bovine oocytes.

Heat shock protein 90 (Hsp90) is critical for cell homeostasis but its role on bovine oocyte maturation is not well known. We investigated the importance of Hsp90 for competence of bovine oocyte using 17-(allylamino)-17-demethoxygeldanamycin (17AAG), an inhibitor of Hsp90, during in vitro maturation (IVM). Three experiments evaluated the effect of 17AAG on developmental competence of oocytes matured in vitro under thermoneutral (38.5ºC) or heat shock (HS; 41.5ºC) temperatures. The first experiment found that the blastocyst rates were lower (P < 0.05) with 2 µM 17AAG compared with the untreated control (0 µM). The abundance of HSF1 transcripts was higher in oocytes matured with 2 µM than with 0 and 1 µM 17AAG, whereas the abundance of HSP90AA1 and HSPA1A transcripts was lower (P < 0.05) with 1 and 2 µM than with 0 µM. The second experiment found that 2 µM 17AAG for 12 or 24 h during IVM decreased (P < 0.05) the blastocysts rates. In the third experiment, the association of 2 μM 17AAG with HS for 12 h during IVM resulted in lower (P < 0.05) blastocysts rates than 17AAG, HS or untreated control. In conclusion, inhibition of Hsp90 during in vitro maturation compromises further embryo development; the association of Hsp90 inhibition with HS aggravates the deleterious effect of both on oocyte developmental competence.

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