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维甲酸诱导水牛(Bubalus bubalis)胚胎干细胞分化为生殖细胞。

Retinoic acid induces differentiation of buffalo (Bubalus bubalis) embryonic stem cells into germ cells.

作者信息

Shah Syed Mohmad, Singla Suresh Kumar, Palta Prabhat, Manik Radhey Sham, Chauhan Manmohan Singh

机构信息

Animal Biotechnology Centre, National Dairy Research Institute, Karnal - 132001, Haryana, India.

Animal Biotechnology Centre, National Dairy Research Institute, Karnal - 132001, Haryana, India.

出版信息

Gene. 2017 Aug 30;626:358-366. doi: 10.1016/j.gene.2017.05.037. Epub 2017 May 17.

Abstract

Development of precise and reproducible culture system for in vitro differentiation of embryonic stem (ES) cells into germ cells counts as a major leap forward for understanding not only the remarkable process of gametogenesis, otherwise obscured by limited availability of precursor primordial germ cells (PGCs), but in finally treating the catastrophic infertility. Taking into account the significant role of retinoic acid (RA) during in vivo gametogenesis, we designed the present study to investigate the effects of its stimulation on directing the differentiation of ES cells into germ cells. The effects of RA were analyzed across dose-and-time upon various stages of gametogenesis like PGC induction, meiosis initiation and completion, haploid cell formation and development of the final gamete (oocyte and spermatozoa). Out of the series of RA doses (2, 4, 8, 16, 20 and 30μM), 16μM RA for 8day culture interval was found to induce highest expression of PGC- and meiosis-associated genes like DAZL, VASA, SYCP3, MLH1, TNP1/2 and PRM2, while mature germ cell genes like BOULE and TEKT1 (Spermatocyte markers), GDF9 and ZP2 (Oocyte markers) showed higher expression at 2μM RA dose, suggesting functional concentration-gradient of RA activity. Immunocytochemistry revealed expression of germ lineage-specific markers like: c-KIT, DAZL and VASA (PGC-markers); SYCP3, MLH1 and PROTAMINE1 (Meiotic-markers); ACROSIN and HAPRIN (Spermatocyte-markers); and GDF9 and ZP4 (Oocyte-markers) in optimally differentiated embryoid bodies (EBs) and adherent cultures. We observed significantly reduced (p<0.05) concentration of 5-methyl-2-deoxycytidine in RA-differentiated EBs which is suggestive of the occurrence of methylation erasure. FACS analysis of optimally differentiated cultures detected 3.07% haploid cell population, indicating completion of meiosis. Oocyte-like structures (OLS) were obtained in adherent differentiated cultures. They had a big nucleus and a zona pellucida (ZP4) coat. They showed progression through 2-cell, 4-cell, 8-cell, morula and blastocyst-like structures upon extended culture beyond 14days.

摘要

开发一种精确且可重复的培养系统,用于将胚胎干细胞(ES细胞)体外分化为生殖细胞,这不仅是理解配子发生这一非凡过程(否则会因原始生殖细胞(PGC)前体的有限可用性而变得模糊不清)的重大飞跃,而且最终对于治疗灾难性不孕症也具有重要意义。考虑到视黄酸(RA)在体内配子发生过程中的重要作用,我们设计了本研究,以探讨其刺激对引导ES细胞分化为生殖细胞的影响。在配子发生的各个阶段,如PGC诱导、减数分裂起始和完成、单倍体细胞形成以及最终配子(卵母细胞和精子)的发育过程中,分析了RA在不同剂量和时间的影响。在一系列RA剂量(2、4、8、16、20和30μM)中,发现16μM RA处理8天培养间隔可诱导PGC和减数分裂相关基因如DAZL、VASA、SYCP3、MLH1、TNP1/2和PRM2的最高表达,而成熟生殖细胞基因如BOULE和TEKT1(精母细胞标记物)、GDF9和ZP2(卵母细胞标记物)在2μM RA剂量下表达较高,这表明RA活性存在功能浓度梯度。免疫细胞化学显示在最佳分化的胚状体(EBs)和贴壁培养物中表达生殖谱系特异性标记物,如:c-KIT、DAZL和VASA(PGC标记物);SYCP3、MLH1和鱼精蛋白1(减数分裂标记物);顶体素和HAPRIN(精母细胞标记物);以及GDF9和ZP4(卵母细胞标记物)。我们观察到在RA分化的EBs中5-甲基-2-脱氧胞苷的浓度显著降低(p<0.05),这表明发生了甲基化消除。对最佳分化培养物的FACS分析检测到3.07%的单倍体细胞群体,表明减数分裂完成。在贴壁分化培养物中获得了卵母细胞样结构(OLS)。它们有一个大细胞核和一层透明带(ZP4)包膜。在延长培养超过14天后,它们显示出通过2细胞、4细胞、8细胞、桑椹胚和囊胚样结构的发育过程。

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