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首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >Minimal concentrations of retinoic acid induce stimulation by retinoic acid 8 and promote entry into meiosis in isolated pregonadal and gonadal mouse primordial germ cells
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Minimal concentrations of retinoic acid induce stimulation by retinoic acid 8 and promote entry into meiosis in isolated pregonadal and gonadal mouse primordial germ cells

机译:最低浓度的视黄酸会诱导视黄酸8刺激,并促进分离的性腺前体和性腺小鼠原始生殖细胞进入减数分裂

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In the present study, we demonstrate that minimal concentrations (≤ nM) of retinoic acid (RA), equivalent to the quantity contaminating serum-containing culture medium, are sufficient to promote meiotic entry and progression through meiotic prophase I (MPI) stages in isolated 12.5-days postcoitum (dpc) XX and XY mouse primordial germ cells (PGCs) in culture. Similarly, we found that the same low RA concentration upregulated or inducedstimulation by retinoic acid 8 (Stra8) in such cells, both at mRNA and protein level. In preleptotene/ leptotene germ cells, STRA8 was localized in nuclear dots that disappeared at later MPI stages. In addition to Stra8, other meiotic genes such as Dmc1 and Rec8 appeared stimulated by RA directly in PGCs with similar concentration-dependent trends. Finally, we found that RA induced Stra8, Sycp3, Dmc1, and Rec8 transcripts, promoting meiotic entry in culture also in pregonadal 10.5-dpc PGCs of both sexes. When cultured isolated from somatic cells, such PGCs, however, were unable to progress through MPI stages, while after entering meiosis, they progressed through MPI when cultured within aorta/gonad/ mesonephros tissues. We conclude that besides RA, germ cell intrinsic factors and other exogenous signals from the surrounding somatic cells are probably necessary for meiotic entryand progression in mouse PGCs.
机译:在本研究中,我们证明了视黄酸(RA)的最小浓度(≤nM),相当于污染含血清的培养基的量,足以促进分离的减数分裂前期I(MPI)阶段的减数分裂进入和进展。培养后12.5天的coitit(dpc)XX和XY小鼠原始生殖细胞(PGC)。同样,我们发现在视黄醛酸8(Stra8)的细胞中,无论是mRNA还是蛋白质水平,相同的低RA浓度都能上调或诱导刺激。在前瘦素/瘦素生殖细胞中,STRA8位于核点中,该核点在MPI后期消失。除Stra8以外,其他减数分裂基因(例如Dmc1和Rec8)似乎也由RA直接刺激了PGC中浓度相似的趋势。最后,我们发现RA诱导了Stra8,Sycp3,Dmc1和Rec8转录本,促进了减数分裂在文化上也进入了男性前性腺10.5dpc PGC中。但是,当从体细胞中分离培养时,这类PGC不能进入MPI阶段,而进入减数分裂后,当在主动脉/性腺/中肾组织中培养时,它们会通过MPI进化。我们得出的结论是,除了RA以外,生殖细胞内在因子和来自周围体细胞的其他外源信号可能是减数分裂进入和小鼠PGC进程所必需的。

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