1. Academic Validation
  2. Noncanonical calcium-independent TRPM4 activation governs intestinal fluid homeostasis

Noncanonical calcium-independent TRPM4 activation governs intestinal fluid homeostasis

  • Nat Commun. 2026 Jan 8;17(1):1253. doi: 10.1038/s41467-025-68014-7.
Yaru Liu # 1 2 Jinhong Hu # 3 Chu Xue # 1 Wenjie Huang # 1 Sofia Ievleva 3 4 Wei Lü 5 6 7 Juan Du 8 9 10 Zhengyu Cao 11 12
Affiliations

Affiliations

  • 1 State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, Jiangsu, China.
  • 2 Jiangsu Provincial Key Laboratory for TCM Evaluation and Translational Development, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, China.
  • 3 Department of Molecular Biosciences, Northwestern University, Evanston, IL, USA.
  • 4 Van Andel Institute, Grand Rapids, MI, USA.
  • 5 Department of Molecular Biosciences, Northwestern University, Evanston, IL, USA. [email protected].
  • 6 Department of Pharmacology, Northwestern University; Feinberg School of Medicine, Chicago, IL, USA. [email protected].
  • 7 Chemistry of Life Processes Institute, Northwestern University, Evanston, IL, USA. [email protected].
  • 8 Department of Molecular Biosciences, Northwestern University, Evanston, IL, USA. [email protected].
  • 9 Department of Pharmacology, Northwestern University; Feinberg School of Medicine, Chicago, IL, USA. [email protected].
  • 10 Chemistry of Life Processes Institute, Northwestern University, Evanston, IL, USA. [email protected].
  • 11 State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing, Jiangsu, China. [email protected].
  • 12 Jiangsu Provincial Key Laboratory for TCM Evaluation and Translational Development, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu, China. [email protected].
  • # Contributed equally.
Abstract

Imbalance in intestinal fluid homeostasis leads to nutrient malabsorption, intestinal tissue destruction, and systemic inflammation. Transient receptor potential melastatin 4 (TRPM4) is a calcium-activated, non-selective monovalent cation channel converting chemical signals (CA2+) into electrical signals (membrane depolarization). Here, we show the TRPM4 channel as a direct target of bisacodyl (BIC), a widely used clinical drug for chronic constipation management, and its active metabolite, deacetyl bisacodyl (DAB). DAB-induced laxative effects are abolished in global and intestinal epithelium-specific TRPM4-knockout mice, establishing the essential role of TRPM4 in intestinal fluid regulation. Furthermore, our structural work reveals DAB bound to an uncharacterized pocket, marking it as a non-Ca2+ TRPM4 agonist and unveiling a noncanonical CA2+-independent activation mechanism. Additionally, we delineate a signaling axis, TRPM4 → VGCC/NCX → ANO1, that governs ion homeostasis in the epithelium. Together, these findings establish TRPM4 as a key regulator of intestinal fluid balance and reveal its noncanonical calcium-independent activation as a therapeutic strategy for constipation.

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