| Literature DB >> 32640190 |
Erika Sugisawa1, Yasunori Takayama2, Naoki Takemura3, Takeshi Kondo4, Shigetsugu Hatakeyama4, Yutaro Kumagai5, Masataka Sunagawa2, Makoto Tominaga6, Kenta Maruyama7.
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.Entities:
Keywords: 5-HT; Piezo1; bone formation; colitis; peristalsis; single-stranded RNA
Year: 2020 PMID: 32640190 DOI: 10.1016/j.cell.2020.06.022
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582