未折叠蛋白反应
FGF21型
内质网
细胞生物学
化学
蛋白质折叠
信号转导
内分泌学
激素
内科学
受体
平衡
细胞内
下调和上调
折叠(DSP实现)
神经酰胺
成纤维细胞生长因子
生物
焊剂(冶金)
生物化学
激素受体
蛋白质生物合成
FGF19型
体内
作者
Gerald Grandl,Ann‐Christine König,Fabian Metzger,Arkadiusz Liskiewicz,Tanja Hefele,Shelly Nason,Aaron Novikoff,Nada Al-Refaie,Md Abdur Rahman,Ahmed Khalil,Qian Zhang,Gustav Colldén,Brian Finan,JONATHAN DOUROS,KIRK HABEGGER,Alberto Cebrian-Serrano,Stefanie M. Hauck,Matthias H. Tschöp,Timo D. Müller
出处
期刊:Cell Metabolism
[Cell Press]
日期:2026-06-16
卷期号:38 (7): 1354-1366.e4
被引量:1
标识
DOI:10.1016/j.cmet.2026.05.011
摘要
Fibroblast growth factor 21 (FGF21) is an endocrine hormone with broad metabolic actions at supraphysiological concentrations but unclear physiological function, related to endoplasmic reticulum (ER) stress. ER stress activates the unfolded protein response (UPR), a cellular repair mechanism that maintains cellular homeostasis during protein folding stress. Using proximity labeling, we assessed the intracellular action of FGF21 at its receptor β-klotho (KLB) and discovered associations with protein folding in the ER, ER stress, and H 2 S production. We found that FGF21 increases enzymatic sulfide production and enhances, but does not initiate, the UPR. This FGF21 action is blunted by genetic or pharmacological inhibition of sulfide signaling and is phenocopied by an H 2 S donor in vivo . FGF21 modulating the UPR requires KLB, and even physiological levels of FGF21 modulate the UPR via increased hepatic H 2 S production. Collectively, we reveal a novel physiological role of FGF21 as an endocrine stress hormone that enhances the UPR via increased sulfide signaling.
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