MANF clears mutant uromodulin in human kidney organoids of autosomal dominant tubulointerstitial kidney disease

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Authors: Chenjian Gu, Yili Fang, Y. M. Wang, Eric Tycksen, Gayathri Kondepati, Chuang Li, Kendrah O. Kidd, Jun Liu, Fumihiko Urano, Maria Lindahl, Anthony J. Bleyer, Srikanth Singamaneni
+2 more Zhao Qing Sun, Ying Maggie Chen
Cited by: 0
References: 3

Abstract

Autosomal dominant tubulointerstitial kidney disease due to uromodulin mutations (ADTKD-UMOD) is one of the leading hereditary kidney diseases. Currently there is no targeted treatment. To illuminate human relevance of mesencephalic astrocyte-derived neurotrophic factor (MANF)-based therapy, we have established patient induced pluripotent stem cell (iPSC)-derived kidney organoid model carrying UMOD p.H177-R185del, the leading mutation causing ADTKD. We have discovered that MANF can directly bind and repress ER calcium release channel IP3R1, thus enhancing AMPK-induced autophagy in a TRIB3-dependent manner. The therapeutic implication of this finding may well be extended to other protein misfolding diseases.

Fields of Study & Subjects

Genetic and Kidney Cyst Diseases Autophagy in Disease and Therapy Renal Diseases and Glomerulopathies

Publication details

Journal / source
Journal of Clinical Investigation
Volume
136
Issue
20
Publication date
25 August 2026
Language
EN