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Wnt信号通路在肾小管损伤中的应激效应功能

The hormetic functions of Wnt pathways in tubular injury.

作者信息

Gröne Elisabeth F, Federico Giuseppina, Nelson Peter J, Arnold Bernd, Gröne Hermann-Josef

机构信息

Department of Cellular and Molecular Pathology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.

Clinical Biochemistry, Ludwig Maximilian University, Munich, Bavaria, Germany.

出版信息

Pflugers Arch. 2017 Aug;469(7-8):899-906. doi: 10.1007/s00424-017-2018-7. Epub 2017 Jul 6.

Abstract

Chronic tubulointerstitial damage with tubular epithelial atrophy and interstitial fibrosis is the hallmark of chronic kidney disease (CKD) and a predictor for progression of CKD.Several experiments have now provided evidence that the Wnt signaling pathways are significantly contributing to atrophy and fibrosis; in contrast, it also has been shown that the Wnt system fosters regenerative processes in acute tubular injury.We now have demonstrated that Dickkopf 3 (DKK3) is an agonist for canonical Wnt signaling in CKD and fosters chronic fibrosing inflammation of the tubulointerstitial compartment. Genetic- and antibody-mediated inhibition of DKK3 leads to a pronounced improvement of tubular differentiation and a reduction in fibrosis.In addition, the secreted glycoprotein DKK3 can be used as a non-invasive urinary marker for the extent of CKD in man.

摘要

伴有肾小管上皮萎缩和间质纤维化的慢性肾小管间质损伤是慢性肾脏病(CKD)的标志,也是CKD进展的预测指标。现在有多项实验表明,Wnt信号通路在萎缩和纤维化过程中发挥了重要作用;相反,也有研究表明,Wnt系统在急性肾小管损伤中促进再生过程。我们现在已经证明,Dickkopf 3(DKK3)是CKD中经典Wnt信号的激动剂,并促进肾小管间质区的慢性纤维化炎症。基因和抗体介导的DKK3抑制可显著改善肾小管分化并减少纤维化。此外,分泌型糖蛋白DKK3可作为人类CKD严重程度的非侵入性尿液标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d277/5541077/563da8e93e7e/424_2017_2018_Fig1_HTML.jpg

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