首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Triptolide is a traditional Chinese medicine-derived inhibitor of polycystic kidney disease
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Triptolide is a traditional Chinese medicine-derived inhibitor of polycystic kidney disease

机译:雷公藤甲素是一种源自中药的多囊肾疾病抑制剂

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摘要

During kidney organogenesis, tubular epithelial cells proliferate until a functional tubule is formed as sensed by cilia bending in response to fluid flow. This flow-induced ciliary mechanosensation opens the calcium (Ca~(2+)) channel polycystin-2 (PC2), resulting in a calcium flux-mediated cell cycle arrest. Loss or mutation of either PC2 or its regulatory protein polycystin-1 (PC1) results in autosomal dominant polycystic kidney disease (ADPKD), characterized by cyst formation and growth and often leading to renal failure and death. Here we show that triptolide, the active diterpene in the traditional Chinese medicine Lei Gong Teng, induces Ca~(2+) release by a PC2-dependent mechanism. Furthermore, in a murine model of ADPKD, triptolide arrests cellular proliferation and attenuates overall cyst formation by restoring Ca~(2+) signaling in these cells. We anticipate that small molecule induction of PC2-dependent calcium release is likely to be a valid therapeutic strategy for ADPKD.
机译:在肾脏器官发生过程中,肾小管上皮细胞增殖,直至通过响应流体流动的纤毛弯曲而感觉到形成功能性小管。血流诱导的纤毛机械感觉打开了钙(Ca〜(2+))通道多囊藻蛋白2(PC2),导致钙通量介导的细胞周期停滞。 PC2或其调节蛋白polycystin-1(PC1)的丢失或突变会导致常染色体显性遗传性多囊肾(ADPKD),其特征是囊肿形成和生长,并经常导致肾衰竭和死亡。在这里,我们显示雷公藤甲素(中药雷公藤中的活性二萜)通过PC2依赖性机制诱导Ca〜(2+)释放。此外,在ADPKD的鼠模型中,雷公藤甲素通过恢复这些细胞中的Ca〜(2+)信号传导来阻止细胞增殖并减弱整体囊肿的形成。我们预期PC2依赖性钙释放的小分子诱导可能是ADPKD的有效治疗策略。

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