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瘦素通过 JAK2/STAT3 和 MEK 1/2 通路对兔模型卵丘-卵母细胞复合物体外成熟和类固醇生成分泌的影响。

Influence of leptin on in vitro maturation and steroidogenic secretion of cumulus-oocyte complexes through JAK2/STAT3 and MEK 1/2 pathways in the rabbit model.

机构信息

Departamento de Fisiología (Fisiología Animal), Facultad de Veterinaria, Universidad Complutense de Madrid, Ciudad Universitaria, s/n, 28040 Madrid, Spain.

出版信息

Reproduction. 2010 Mar;139(3):523-32. doi: 10.1530/REP-09-0309. Epub 2009 Dec 23.

Abstract

Extreme body mass indexes may impair reproductive outcome in assisted reproductive technologies. Leptin reflects the amount of body fat and could act as a modulator of oocyte quality through activation of specific transcription factors. The aim of this work was to establish whether: 1) leptin influences meiotic and cytoplasmic oocyte maturation; 2) STAT3 and MAPK mediate the effects of leptin and 3) leptin modulates steroid secretion by cumulus-oocyte complexes (COC) during in vitro maturation (IVM). We confirmed immunolocalisation of leptin receptor in oocytes, cumulus/granulosa cells during the peri-ovulatory period. The confocal study showed that COC supplemented with 1, 10 and 100 ng/ml leptin had a significantly higher metaphase II (MII) percentage than those IVM without leptin (P<0.05) and a similar MII index compared to the group supplemented with 10% FCS. Leptin did not increase the percentage of cytoplasmically matured oocytes in terms of cortical granule migration rate, whereas a significantly higher index was found in the FCS group (P<0.001). Oestradiol concentrations in spent media were higher in the FCS group compared to other treatments (P<0.001). Leptin-stimulated nuclear oocyte maturation was significantly impaired when leptin-induced JAK2/STAT3 and MEK 1/2 activation was suppressed by the inhibitors (P<0.001). Steroid secretion of COC was not affected by leptin activation of JAK2/STAT3 or MEK 1/2 pathways. In conclusion, JAK2/STAT3 and MEK 1/2 pathways mediate the enhancement of nuclear oocyte maturation by leptin; however, neither cytoplasmic oocyte maturation nor steroidogenic response of COC were improved in the present rabbit model.

摘要

极端的体重指数可能会影响辅助生殖技术的生殖结局。瘦素反映了体脂肪量,并可通过激活特定的转录因子来充当卵母细胞质量的调节剂。本研究旨在确定:1)瘦素是否影响卵母细胞的减数分裂和细胞质成熟;2)STAT3 和 MAPK 是否介导瘦素的作用;3)瘦素是否调节体外成熟(IVM)期间卵丘-卵母细胞复合物(COC)的类固醇分泌。我们证实了在排卵前期间卵母细胞、卵丘/颗粒细胞中瘦素受体的免疫定位。共聚焦研究表明,与无瘦素 IVM 的 COC 相比,补充 1、10 和 100ng/ml 瘦素的 COC 的中期 II(MII)比例显著更高(P<0.05),并且与补充 10%FCS 的组具有相似的 MII 指数。瘦素并未增加细胞质成熟卵母细胞的比例,表现为皮质颗粒迁移率,但在 FCS 组中发现的比例显著更高(P<0.001)。与其他处理相比,FCS 组的培养上清液中的雌二醇浓度更高(P<0.001)。当通过抑制剂抑制瘦素诱导的 JAK2/STAT3 和 MEK 1/2 激活时,瘦素刺激的核卵母细胞成熟显著受损(P<0.001)。COC 的类固醇分泌不受瘦素激活 JAK2/STAT3 或 MEK 1/2 途径的影响。总之,JAK2/STAT3 和 MEK 1/2 途径介导了瘦素对核卵母细胞成熟的增强作用;然而,在本兔模型中,卵母细胞的细胞质成熟或 COC 的类固醇生成反应均未得到改善。

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