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Epigenetic transcriptional reprogramming by WT1 mediates a repair response during podocyte injury

机译:通过WT1的表观遗传转录重新编程介导在足细胞损伤期间修复反应

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In the context of human disease, the mechanisms whereby transcription factors reprogram gene expression in reparative responses to injury are not well understood. We have studied the mechanisms of transcriptional reprogramming in disease using murine kidney podocytes as a model for tissue injury. Podocytes are a crucial component of glomeruli, the filtration units of each nephron. Podocyte injury is the initial event in many processes that lead to end-stage kidney disease. Wilms tumor-1 (WT1) is a master regulator of gene expression in podocytes, binding nearly all genes known to be crucial for maintenance of the glomerular filtration barrier. Using murine models and human kidney organoids, we investigated WT1-mediated transcriptional reprogramming during the course of podocyte injury. Reprogramming the transcriptome involved highly dynamic changes in the binding of WT1 to target genes during a reparative injury response, affecting chromatin state and expression levels of target genes.
机译:在人类疾病的背景下,转录因子重新编程基因表达在重复损伤中的转录基因表达的机制尚不清楚。我们研究了使用小鼠肾小段细胞作为组织损伤模型的疾病转录重编程的机制。龟粒细胞是肾小球的关键组分,每个肾的过滤单元。 Podocyte损伤是许多过程中导致终级肾病的初始事件。 Wilms肿瘤-1(wt1)是龟粒细胞中基因表达的主调节剂,几乎所有已知的所有基因都对维持肾小球过滤屏障至关重要。使用小鼠模型和人肾有机体,我们研究了在致统粒细胞损伤过程中的WT1介导的转录重编程。重新编程转录组涉及WT1与靶基因结合的高度动态变化在重新损伤响应期间,影响染色质状态和靶基因的表达水平。

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