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Chicken stem cell factor enhances primordial germ cell proliferation cooperatively with fibroblast growth factor 2

机译:鸡干细胞因子与成纤维细胞生长因子2协同增强原始生殖细胞的增殖

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摘要

An in vitro culture system of chicken primordial germ cells (PGCs) has been recently developed, but the growth factor involved in the proliferation of PGCs is largely unknown. In the present study, we investigated the growth effects of chicken stem cell factor (chSCF) on the in vitro proliferation of chicken PGCs. We established two feeder cell lines (buffalo rat liver cells; BRL cells) that stably express the putative secreted form of chSCF (chSCF1-BRL) and membrane bound form of chSCF (chSCF2-BRL). Cultured PGC lines were incubated on chSCF1 or chSCF2-BRL feeder cells with fibroblast growth factor 2 (FGF2), and growth effects of each chSCF isoform were investigated. The in vitro proliferation rate of the PGCs cultured on chSCF2-BRL at 20 days of culture was more than threefold higher than those cultured on chSCF1-BRL cells and more than fivefold higher than those cultured on normal BRL cells. Thus, use of chSCF2-BRL feeder layer was effective for in vitro proliferation of chicken PGCs. However, the acceleration of PGC proliferation on chSCF2-BRL was not observed without FGF2, suggesting that chSCF2 would act as a proliferation co-factor of FGF2. We transferred the PGCs cultured on chSCF2-BRL cells to recipient embryos, generated germline chimeric chickens and assessed the germline competency of cultured PGCs by progeny test. Donor-derived progenies were obtained, and the frequency of germline transmission was 3.39%. The results of this study demonstrate that chSCF2 induces hyperproliferation of chicken PGCs retaining germline competency in vitro in cooperation with FGF2.
机译:最近已经开发了鸡原始生殖细胞(PGCs)的体外培养系统,但是很大程度上未知PGCs增殖所涉及的生长因子。在本研究中,我们研究了鸡干细胞因子(chSCF)对鸡PGC体外增殖的生长作用。我们建立了两个饲养细胞系(水牛大鼠肝细胞; BRL细胞),它们稳定表达推定的chSCF形式(chSCF1-BRL)和膜结合形式的chSCF(chSCF2-BRL)。将培养的PGC品系在具有成纤维细胞生长因子2(FGF2)的chSCF1或chSCF2-BRL饲养细胞上孵育,并研究每种chSCF亚型的生长效果。在chSCF2-BRL上培养20天的PGC的体外增殖速率比在chSCF1-BRL细胞上培养的PGC的体外增殖速率高三倍以上,并且比在正常BRL细胞上培养的PGC的体外增殖速率高五倍以上。因此,使用chSCF2-BRL饲养层对鸡PGC的体外增殖有效。但是,没有FGF2时,未观察到chSCF2-BRL上PGC增殖的加速,这表明chSCF2将充当FGF2的增殖辅助因子。我们将在chSCF2-BRL细胞上培养的PGC转移到受体胚胎,生成了种系嵌合鸡,并通过后代测试评估了培养的PGC的种系能力。获得了供体来源的后代,种系传播的频率为3.39%。这项研究的结果表明chSCF2与FGF2协同诱导了在体外保持种系能力的鸡PGC的过度增殖。

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