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首页> 外文期刊>Stem Cell Research & Therapy >Establishment of human trophoblast stem cells from human induced pluripotent stem cell-derived cystic cells under micromesh culture
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Establishment of human trophoblast stem cells from human induced pluripotent stem cell-derived cystic cells under micromesh culture

机译:在微孔培养下由人诱导的多能干细胞衍生的囊性细胞建立人滋养层干细胞

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Trophoblasts as a specific cell lineage are crucial for the correct function of the placenta. Human trophoblast stem cells (hTSCs) are a proliferative population that can differentiate into syncytiotrophoblasts and extravillous cytotrophoblasts. Many studies have reported that chemical supplements induce the differentiation of trophoblasts from human induced pluripotent stem cells (hiPSCs). However, there have been no reports of the establishment of proliferative hTSCs from hiPSCs. Our previous report showed that culturing hiPSCs on micromesh as a bioscaffold induced cystic cells with trophoblast properties. Here, we aimed to establish hTSCs from hiPSCs. We used the micromesh culture technique to induce hiPSC differentiation into trophoblast cysts. We then reseeded and purified cystic cells. The cells derived from the reseeded cysts were highly proliferative. Low expression levels of pluripotency genes and high expression levels of TSC-specific genes were detected in proliferative cells. The cells could be passaged, and further directional differentiation into syncytiotrophoblast- and extravillous cytotrophoblast-like cells was confirmed by marker expression and hormone secretion. We established hiPSC-derived hTSCs, which may be applicable for studying the functions of trophoblasts and the placenta. Our experimental system may provide useful tools for understanding the pathogenesis of infertility owing to trophoblast defects in the future.
机译:滋养细胞是一种特定的细胞谱系,对于胎盘的正确功能至关重要。人滋养层干细胞(hTSC)是一种增殖性种群,可以分化为合体滋养层滋养细胞和绒毛外滋养层滋养细胞。许多研究报告说,化学补品可诱导滋养细胞从人诱导的多能干细胞(hiPSC)分化。但是,尚无关于从hiPSC建立增生hTSC的报道。我们以前的报告表明,在micromesh上培养hiPSC作为生物支架诱导的具有滋养细胞特性的囊性细胞。在这里,我们旨在从hiPSC建立hTSC。我们使用了微孔培养技术来诱导hiPSC分化为滋养细胞囊肿。然后,我们重新播种和纯化了囊性细胞。来源于再播囊肿的细胞高度增殖。在增殖细胞中检测到多能性基因的低表达水平和TSC特异性基因的高表达水平。可以传代细胞,并通过标记物表达和激素分泌证实进一步定向分化为合体滋养层细胞和绒毛外滋养细胞样细胞。我们建立了hiPSC衍生的hTSC,可用于研究滋养细胞和胎盘的功能。我们的实验系统可能会提供有用的工具,以了解将来由于滋养细胞缺陷引起的不孕症的发病机理。

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