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瘦素通过不依赖卵丘细胞和依赖卵丘细胞的机制促进牛卵母细胞的减数分裂进程和发育能力。

Leptin promotes meiotic progression and developmental capacity of bovine oocytes via cumulus cell-independent and -dependent mechanisms.

作者信息

Paula-Lopes Fabíola F, Boelhauve Marc, Habermann Felix A, Sinowatz Fred, Wolf Eckhard

机构信息

Institute of Molecular Animal Breeding and Biotechnology, Ludwig-Maximilians University, 81377 Munich, Germany.

出版信息

Biol Reprod. 2007 Mar;76(3):532-41. doi: 10.1095/biolreprod.106.054551. Epub 2006 Nov 8.

Abstract

Leptin has been shown to exert positive effects during the maturation of bovine oocytes, influencing blastocyst development, apoptosis, and the transcript levels of developmentally important genes. The present study was conducted to characterize further the mechanisms of leptin action on oocytes and the role of cumulus cells (CCs) in this context. In the first series of experiments, cumulus-oocyte complexes (COCs) were matured in serum-free medium that contained 0, 1 or 10 ng/ml leptin or in medium that was supplemented with 10% (v/v) estrus cow serum (ECS). Leptin concentrations of 1 and 10 ng/ml stimulated the meiotic progression of oocytes. Moreover, TUNEL staining demonstrated that these leptin doses reduced the proportion of apoptotic CCs. In the second series of experiments, COCs or denuded oocytes (DOs) were matured in the presence of 0 or 10 ng/ml leptin. The percentages of COCs and DOs with extruded polar bodies were increased by leptin. In contrast, positive effects of leptin on fertilization rates and blastocyst development were only observed after treatment of COCs but not of DOs. Leptin treatment of COCs consistently enhanced blastocyst development even after parthenogenetic activation of oocytes or after the removal of CCs before fertilization. The proportion of polyspermic oocytes was not affected by leptin treatment or oocyte denudation. In the third series of experiments, COCs were matured in the presence of 0, 1 or 10 ng/ml leptin. The transcript levels of specific genes were determined by reverse transcriptase-quantitative PCR (RT-qPCR) analysis of cumulus cells and single oocytes. Leptin treatment increased the levels of FAS, FASLG, and STAT3 transcripts in oocytes, but did not affect the LEPR, BAX, and BIRC4 mRNA concentrations. In cumulus cells, leptin treatment increased the mRNA levels for LEPR, STAT3, BAX, BIRC4, and FAS, but did not alter FASLG mRNA abundance. In conclusion, leptin differentially regulates gene expression in oocytes and cumulus cells. Moreover, leptin enhances both oocyte maturation and developmental capacity via cumulus cell-independent and -dependent mechanisms.

摘要

已证明瘦素在牛卵母细胞成熟过程中发挥积极作用,影响囊胚发育、细胞凋亡以及发育重要基因的转录水平。本研究旨在进一步阐明瘦素对卵母细胞的作用机制以及卵丘细胞(CCs)在此过程中的作用。在第一组实验中,卵丘 - 卵母细胞复合体(COCs)在含有0、1或10 ng/ml瘦素的无血清培养基中成熟,或在补充有10%(v/v)发情母牛血清(ECS)的培养基中成熟。1和10 ng/ml的瘦素浓度刺激了卵母细胞的减数分裂进程。此外,TUNEL染色表明这些瘦素剂量降低了凋亡CCs的比例。在第二组实验中,COCs或裸卵(DOs)在0或10 ng/ml瘦素存在下成熟。瘦素增加了排出极体的COCs和DOs的百分比。相比之下,仅在处理COCs后观察到瘦素对受精率和囊胚发育的积极影响,而对DOs则未观察到。即使在卵母细胞孤雌激活后或在受精前去除CCs后,用瘦素处理COCs也始终能增强囊胚发育。多精受精卵母细胞的比例不受瘦素处理或卵母细胞去卵丘的影响。在第三组实验中,COCs在0、1或10 ng/ml瘦素存在下成熟。通过对卵丘细胞和单个卵母细胞进行逆转录 - 定量PCR(RT - qPCR)分析来测定特定基因的转录水平。瘦素处理增加了卵母细胞中FAS、FASLG和STAT3的转录水平,但不影响LEPR、BAX和BIRC4的mRNA浓度。在卵丘细胞中,瘦素处理增加了LEPR、STAT3、BAX、BIRC4和FAS的mRNA水平,但未改变FASLG的mRNA丰度。总之,瘦素差异调节卵母细胞和卵丘细胞中的基因表达。此外,瘦素通过不依赖和依赖卵丘细胞的机制增强卵母细胞成熟和发育能力。

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