Dynamic palmitoylation of STX11 controls injury-induced fatty acid uptake to promote muscle regeneration

STX11 的动态棕榈酰化控制损伤引起的脂肪酸吸收以促进肌肉再生

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作者:Juan Wang, Dong-Lin Li, Lang-Fan Zheng, Su Ren, Zi-Qin Huang, Ying Tao, Ziyu Liu, Yanxia Shang, Dejian Pang, Huiling Guo, Taoling Zeng, Hong-Rui Wang, He Huang, Xingrong Du, Haobin Ye, Hai-Meng Zhou, Peng Li, Tong-Jin Zhao

Abstract

Different types of cells uptake fatty acids in response to different stimuli or physiological conditions; however, little is known about context-specific regulation of fatty acid uptake. Here, we show that muscle injury induces fatty acid uptake in muscle stem cells (MuSCs) to promote their proliferation and muscle regeneration. In humans and mice, fatty acids are mobilized after muscle injury. Through CD36, fatty acids function as both fuels and growth signals to promote MuSC proliferation. Mechanistically, injury triggers the translocation of CD36 in MuSCs, which relies on dynamic palmitoylation of STX11. Palmitoylation facilitates the formation of STX11/SNAP23/VAMP4 SANRE complex, which stimulates the fusion of CD36- and STX11-containing vesicles. Restricting fatty acid supply, blocking fatty acid uptake, or inhibiting STX11 palmitoylation attenuates muscle regeneration in mice. Our studies have identified a critical role of fatty acids in muscle regeneration and shed light on context-specific regulation of fatty acid sensing and uptake.

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