科研速览 · Science Skim继续刷下去 · Keep skimming →
◆ Journal of Clinical Investigation2026-08-25· Tamm–Horsfall protein

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

Chenjian Gu, Yili Fang, Y. M. Wang, Eric Tycksen, Gayathri Kondepati, Chang Li, Kendrah Kidd, Jun Liu, Fumihiko Urano, Maria Lindahl, AJ Bleyer, Srikanth Singamaneni, Zhao Sun, Ying Maggie Chen

原始摘要(英文原文)· Original 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.
读原文 · Read the paper ↗

AI 追问PRO

登录后使用 AI 追问

讨论区

登录后参与讨论

相关论文 · Related

MANF clears mutant uromodulin in human kidney organoids of autosomal dominant tubulointerstitial kidney disease — 科研速览 Science Skim