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Generation of Chemically Induced Liver Progenitors (CLiPs) from Rat Adult Hepatocytes

机译:从大鼠成人肝细胞产生化学诱导的肝脏祖细胞(夹子)

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摘要

Primary mature hepatocytes (MHs) or their progenitor cells are candidate cell sources for cell transplantation therapy in severe liver diseases. However, stable culture of these cells or generation of equivalent cells from pluripotent stem cells has been limited. Using a cocktail of small molecules that we previously found useful in stable culture of multiple types of stem/progenitor cells, we recently established a novel method to generate bipotent liver progenitor cells, named chemically induced liver progenitors (CLiPs), from adult rat MHs. Here, we describe a detailed protocol for the induction of rat CLiPs. We first describe the method to isolate primary rat MHs and then describe how to induce CLiPs from these MHs. In addition, we describe a method to evaluate the bipotentiality of generated CLiPs to differentiate into hepatocytes and biliary epithelial cells. We also describe how to establish stable CLiPs through long-term culture with detailed example data. Primary CLiPs can be generated within 2 weeks, and stable CLiPs, which undergo 10 passages, can be established within 2.5-4 months with batch-to-batch variability.
机译:主要成熟肝细胞(MHS)或其祖细胞是严重肝病细胞移植治疗的候选细胞来源。然而,这些细胞的稳定培养或来自多能干细胞的同等细胞的产生受到限制。使用我们之前发现的小分子的鸡尾酒在多种类型的茎/祖细胞的稳定培养物中,我们最近建立了一种新的方法,从成年大鼠MHS产生了名为化学诱导的肝祖细胞(夹子)的Bipotent肝祖细胞。在这里,我们描述了对大鼠夹子诱导的详细方案。我们首先描述了隔离原代大鼠MHS的方法,然后描述如何从这些MHS诱导剪辑。此外,我们描述了评估生成夹子的Bipotity以区分成肝细胞和胆道上皮细胞的方法。我们还描述了如何通过具有详细示例数据的长期文化建立稳定的剪辑。初级剪辑可以在2周内产生,并且可以在2.5-4个月内建立稳定的夹子,分批到批量变异。

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