TRPA1 regulates gastrointestinal motility through serotonin release from enterochromaffin cells

Katsura Nozawa(Astellas Pharma (Japan)), Eri Kawabata-Shoda(Astellas Pharma (Japan)), Hitoshi Doihara(Astellas Pharma (Japan)), Ryosuke Kojima(Astellas Pharma (Japan)), Hidetsugu Okada(Astellas Pharma (Japan)), Shinobu Mochizuki(Astellas Pharma (Japan)), Yorikata Sano(Astellas Pharma (Japan)), Kohei Inamura(Astellas Pharma (Japan)), Hitoshi Matsushime(Astellas Pharma (Japan)), Tomonobu Koizumi(Astellas Pharma (Japan)), Toshihide Yokoyama(Astellas Pharma (Japan)), Hiroyuki Ito(Astellas Pharma (Japan))
Proceedings of the National Academy of Sciences
February 12, 2009
Cited by 403

Abstract

Serotonin (5-hydroxytryptamine; 5-HT) is abundantly present throughout the gastrointestinal tract and stored mostly in enterochromaffin (EC) cells, which are located on the mucosal surface. 5-HT released from EC cells stimulate both intrinsic and extrinsic nerves, which results in various physiological and pathophysiological responses, such as gastrointestinal contractions. EC cells are believed to have the ability to respond to the chemical composition of the luminal contents of the gut; however, the underlying molecular and cellular mechanisms have not been identified. Here, we demonstrate that the transient receptor potential (TRP) cation channel TRPA1, which is activated by pungent compounds or cold temperature, is highly expressed in EC cells. We also found that TRPA1 agonists, including allyl isothiocyanate and cinnamaldehyde, stimulate EC cell functions, such as increasing intracellular Ca(2+) levels and 5-HT release, by using highly concentrated EC cell fractions and a model of EC cell function, the RIN14B cell line. Furthermore, we showed that allyl isothiocyanate promotes the contraction of isolated guinea pig ileum via the 5-HT(3) receptor. Taken together, our results indicate that TRPA1 acts as a sensor molecule for EC cells and may regulate gastrointestinal function.


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