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The Pathogenic Role of Notch Activation in Podocytes

机译:Notch激活在足细胞中的致病作用

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摘要

Podocytes play a key role in the maintenance of glomerular filtration barrier. Depletion or dysregulative mechanisms of podocytes can lead to the development of glomerulosclerosis. Signaling pathways that control these processes in podocytes are not fully understood. Recent studies from our and other laboratories found that genes that belong to the Notch pathway are regulated in patients and in animal models of renal disease. Genetic studies performed on mice with conditional expression of active Notch1 protein showed massive albuminuria, glomerulosclerosis ultimately renal failure and death of the animals. Gamma secretase inhibitors and genetic deletion of Notch transcriptional binding partner (Rbpj) protected animals from nephrotic syndrome. Further studies are needed to define whether the activation of Notch pathway in podocytes represents a common pathomechanism in glomerular injury and its potential to be a therapeutic target for the treatment of chronic kidney disease.
机译:足细胞在维持肾小球滤过屏障中起关键作用。足细胞的耗竭或失调机制可导致肾小球硬化的发展。尚未完全了解控制足细胞中这些过程的信号通路。我们和其他实验室的最新研究发现,Notch通路的基因在患者和肾脏疾病的动物模型中受到调控。对有条件表达活性Notch1蛋白的小鼠进行的遗传研究显示,大量蛋白尿,肾小球硬化最终导致肾衰竭和动物死亡。 γ分泌酶抑制剂和Notch转录结合伴侣(Rbpj)的基因删除可保护动物免受肾病综合症的侵害。需要进一步的研究来确定足细胞中Notch途径的活化是否代表肾小球损伤中的常见病理机制,以及其是否可能成为治疗慢性肾脏疾病的治疗靶标。

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