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  2. Piezo1 regulates colon stem cells to maintain epithelial homeostasis through SCD1-Wnt-β-catenin and programming fatty acid metabolism

Piezo1 regulates colon stem cells to maintain epithelial homeostasis through SCD1-Wnt-β-catenin and programming fatty acid metabolism

  • Cell Rep. 2025 Mar 25;44(3):115400. doi: 10.1016/j.celrep.2025.115400.
Feifei Fang 1 Gangping Li 1 Xueyan Li 1 Jiandi Wu 1 Ying Liu 1 Haoren Xin 1 Zhe Wang 1 Jianhua Fang 1 Yudong Jiang 1 Wei Qian 1 Xiaohua Hou 1 Jun Song 2
Affiliations

Affiliations

  • 1 Department of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
  • 2 Department of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China. Electronic address: 2011xh0869@hust.edu.cn.
Abstract

Piezo1, which maintains the integrity and function of the intestinal epithelial barrier, is essential for colonic epithelial homeostasis. However, whether and how Piezo1 regulates colon stem cell fate remains unclear. Here, we show that Piezo1 inhibition promotes colon stem cell proliferation. Mechanistically, stearoyl-CoA 9-desaturase 1 (SCD1) is downstream of Piezo1 to affect colon stem cell stemness by acting on the Wnt-β-catenin pathway. For mice, the altered colon stem cell stemness after Piezo1 knockdown and activation was accompanied by a reprogrammed fatty acid (FA) metabolism in colon crypts. Notably, we found that GsMTX4 protects injured colon stem cell stemness in mouse and human colitis organoids. Our results elucidated the role of Piezo1 in regulating normal and postinjury colon stem cell fates through SCD1-Wnt-β-catenin and the SCD1-mediated FA desaturation process. These results provide fresh perspectives on the mechanical factors regulating colon stem cell fate and therapeutic strategies for related intestinal diseases.

Keywords

CP: Metabolism; CP: Stem cell research; Piezo1; SCD1; colitis; colon stem cell; fatty acid metabolism; intestinal epithelial homeostasis.

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