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Reprogramming of Various Cell Types to a Beta-Like State by Pdx1 Ngn3 and MafA

机译:通过Pdx1Ngn3和MafA将各种细胞类型重新编程为类似Beta的状态

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摘要

The three transcription factors, PDX1, NGN3 and MAFA, are very important in pancreatic development. Overexpression of these three factors can reprogram both pancreatic exocrine cells and SOX9-positive cells of the liver into cells resembling pancreatic beta cells. In this study we investigate whether other cell types can be reprogrammed. Eight cell types are compared and the results are consistent with the idea that reprogramming occurs to a greater degree for developmentally related cells (pancreas, liver) than for other types, such as fibroblasts. Using a line of mouse hepatocyte-derived cells we screened 13 compounds for the ability to increase the yield of reprogrammed cells. Three are active and when used in combination they can increase the yield of insulin-immunopositive cells by a factor of six. These results should contribute to the eventual ability to develop a new cure for diabetes based on the ability to reprogram other cells in the body to a beta cell phenotype.
机译:PDX1,NGN3和MAFA这三个转录因子在胰腺发育中非常重要。这三个因素的过表达可以将胰腺的外分泌细胞和肝脏的SOX9阳性细胞重新编程为类似于胰腺β细胞的细胞。在这项研究中,我们调查其他细胞类型是否可以重新编程。比较了八种细胞类型,结果与这样的想法是一致的:与其他类型的细胞(如成纤维细胞)相比,与发育相关的细胞(胰腺,肝脏)发生更大程度的重编程。使用一系列小鼠肝细胞来源的细胞,我们筛选了13种化合物来提高重编程细胞产量的能力。三种是有活性的,当组合使用时,它们可以使胰岛素免疫阳性细胞的产量提高六倍。这些结果应有助于根据将体内其他细胞重编程为β细胞表型的能力,最终开发出一种新的糖尿病治疗方法。

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