RNA Sensing by Gut Piezo1 Is Essential for Systemic Serotonin Synthesis

Cell. 2020 Aug 6;182(3):609-624.e21. doi: 10.1016/j.cell.2020.06.022. Epub 2020 Jul 7.

Abstract

Gastrointestinal enterochromaffin cells regulate bone and gut homeostasis via serotonin (5-hydroxytryptamine [5-HT]) production. A recent report suggested that gut microbes regulate 5-HT levels; however, the precise underlying molecular mechanisms are unexplored. Here, we reveal that the cation channel Piezo1 in the gut acts as a sensor of single-stranded RNA (ssRNA) governing 5-HT production. Intestinal epithelium-specific deletion of mouse Piezo1 profoundly disturbed gut peristalsis, impeded experimental colitis, and suppressed serum 5-HT levels. Because of systemic 5-HT deficiency, conditional knockout of Piezo1 increased bone formation. Notably, fecal ssRNA was identified as a natural Piezo1 ligand, and ssRNA-stimulated 5-HT synthesis from the gut was evoked in a MyD88/TRIF-independent manner. Colonic infusion of RNase A suppressed gut motility and increased bone mass. These findings suggest gut ssRNA as a master determinant of systemic 5-HT levels, indicating the ssRNA-Piezo1 axis as a potential prophylactic target for treatment of bone and gut disorders.

Keywords: 5-HT; Piezo1; bone formation; colitis; peristalsis; single-stranded RNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / metabolism
  • Animals
  • Bone and Bones / cytology
  • Bone and Bones / metabolism*
  • Calcium / metabolism
  • Colitis / genetics
  • Colitis / metabolism
  • Colitis / prevention & control
  • Colon / metabolism*
  • Colon / physiology
  • Feces / chemistry
  • Female
  • Gastrointestinal Motility / genetics*
  • Gastrointestinal Motility / physiology
  • HEK293 Cells
  • Humans
  • Immunohistochemistry
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / metabolism
  • Ion Channels / genetics
  • Ion Channels / metabolism*
  • Ligands
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microbiota / drug effects
  • Myeloid Differentiation Factor 88 / metabolism
  • Osteoclasts / metabolism
  • Pyrazines / pharmacology
  • RNA / metabolism*
  • RNA / pharmacology
  • Ribonuclease, Pancreatic / administration & dosage
  • Serotonin / biosynthesis*
  • Serotonin / blood
  • Serotonin / deficiency
  • Serotonin / metabolism*
  • Thiadiazoles / pharmacology

Substances

  • Adaptor Proteins, Vesicular Transport
  • Ion Channels
  • Ligands
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • Piezo1 protein, mouse
  • Pyrazines
  • TICAM-1 protein, mouse
  • Thiadiazoles
  • yoda-1
  • Serotonin
  • RNA
  • Ribonuclease, Pancreatic
  • Calcium