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Treatment with retinoic acid and lens epithelial cell-conditioned medium in vitro directed the differentiation of pluripotent stem cells towards corneal endothelial cell-like cells

机译:视黄酸和晶状体上皮细胞条件培养基的体外处理可将多能干细胞分化为角膜内皮细胞样细胞

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Embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) have extensive self-renewal capacity and the potential to differentiate into all tissue-specific cell lineages, including corneal endothelial cells (CECs). They are a promising prospect for the future of regenerative medicine. The method of derivation of CECs from ESCs and iPSCs, however, remains to be elucidated. In this study, mouse ESCs and iPSCs were induced to differentiate into CECs using CEC embryonic development events as a guide. All-trans retinoic acid (RA) treatment during the embryoid body (EB) differentiation step was used to promote neural crest (NC) cell differentiation as first step and was followed by a second induction in CEC- or lens epithelial cell (LEC)-conditioned medium (CM) to ultimately generate CEC-like cells. During the corresponding differentiation stages, NC developmental markers and CEC differentiation markers were detected at the protein level using immunocytochemistry (ICC) and at the mRNA level by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). During the first stage, the data indicated that 4 days of treatment with 1 mu M RA starting on day 4 of EB formation favored NC cell differentiation and that plating on gelatin-coated plates led to cell migration out of the EBs. The second-stage differentiation results showed that the CM, particularly the LEC-CM, enhanced the yield of polygonal cells with CEC-specific marker expression shown by ICC and RT-qPCR. This study demonstrates that mouse ESCs and iPSCs were induced and expressed CEC differentiation markers when subjected to a two-step inducement process, suggesting that they are a promising resource for corneal endothelium failure replacement therapy in the future.
机译:胚胎干细胞(ESC)和诱导性多能干细胞(iPSC)具有广泛的自我更新能力,并且具有分化为包括角膜内皮细胞(CEC)在内的所有组织特异性细胞谱系的潜力。它们是再生医学未来的有希望的前景。然而,尚需阐明从ESC和iPSC衍生CEC的方法。在这项研究中,以CEC胚胎发育事件为指导,诱导小鼠ESC和iPSC分化为CEC。第一步是在胚状体(EB)分化步骤中进行全反式维甲酸(RA)处理,以促进神经rest(NC)细胞分化,然后在CEC-或晶状体上皮细胞(LEC)-中进行第二次诱导。条件培养基(CM)最终产生CEC样细胞。在相应的分化阶段,通过免疫细胞化学(ICC)在蛋白质水平检测mRNA水平,通过逆转录定量聚合酶链反应(RT-qPCR)在mRNA水平检测NC发育标志物和CEC分化标志物。在第一阶段,数据表明从EB形成的第4天开始,用1μM RA处理4天有利于NC细胞分化,而在明胶包被的板上进行铺板会导致细胞迁移出EB。第二阶段的分化结果表明,CM,特别是LEC-CM,通过ICC和RT-qPCR显示具有CEC特异性标志物表达的多角形细胞的产量提高。这项研究表明,小鼠胚胎干细胞和iPSCs经过两步诱导过程后被诱导并表达CEC分化标记,这表明它们是将来角膜内皮衰竭替代治疗的有希望的资源。

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