Miyake, Masato Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Zhang, Jun Tokushima University|ER Stress Research Institute
Hisanaga, Satoshi Tokushima University|Kumamoto University
Tsugawa, Kazue Tokushima University
Sakaue, Hiroshi Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Oyadomari, Miho Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Kiyonari, Hiroshi RIKEN
Oyadomari, Seiichi Tokushima University|ER Stress Research Institute Tokushima University Educator and Researcher Directory KAKEN Search Researchers
The eIF2α phosphorylation-dependent integrated stress response (ISR) is a signaling pathway that maintains homeostasis in mammalian cells exposed to various stresses. Here, ISR activation in adipocytes improves obesity and diabetes by regulating appetite in a non-cell-autonomous manner. Adipocyte-specific ISR activation using transgenic mice decreases body weight and improves glucose tolerance and obesity induced by a high-fat diet (HFD) via preferential inhibition of HFD intake. The transcriptome analysis of ISR-activated adipose tissue reveals that growth differentiation factor 15 (GDF15) expression is induced by the ISR through the direct regulation of the transcription factors ATF4 and DDIT3. Deficiency in the GDF15 receptor GFRAL abolishes the adipocyte ISR-dependent preferential inhibition of HFD intake and the anti-obesity effects. Pharmacologically, 10(E), 12(Z)-octadecadienoic acid induces ISR-dependent GDF15 expression in adipocytes and decreases the intake of the HFD. Based on our findings the specific activation of the ISR in adipocytes controls the non-cell-autonomous regulation of appetite.
This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
|DOI (Published Version)|
|URL ( Publisher's Version )|
isci_24_12_103448.pdf 3.83 MB
Institute of Advanced Medical Sciences