Interstitial cells of Cajal integrate excitatory and inhibitory neurotransmission with intestinal slow-wave activity

The enteric nervous system contains excitatory and inhibitory neurons, which control contraction and relaxation of smooth muscle cells as well as gastrointestinal motor activity. Little is known about the exact cellular mechanisms of neuronal signal transduction to smooth muscle cells in the gut. He...

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Veröffentlicht in:Nature communications 2013, Vol.4 (1), p.1630-1630, Article 1630
Hauptverfasser: Klein, Sabine, Seidler, Barbara, Kettenberger, Anna, Sibaev, Andrei, Rohn, Michael, Feil, Robert, Allescher, Hans-Dieter, Vanderwinden, Jean-Marie, Hofmann, Franz, Schemann, Michael, Rad, Roland, Storr, Martin A., Schmid, Roland M., Schneider, Günter, Saur, Dieter
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Sprache:eng
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Zusammenfassung:The enteric nervous system contains excitatory and inhibitory neurons, which control contraction and relaxation of smooth muscle cells as well as gastrointestinal motor activity. Little is known about the exact cellular mechanisms of neuronal signal transduction to smooth muscle cells in the gut. Here we generate a c-Kit CreERT2 knock-in allele to target a distinct population of pacemaker cells called interstitial cells of Cajal. By genetic loss-of-function studies, we show that interstitial cells of Cajal, which generate spontaneous electrical slow waves and thus rhythmic contractions of the smooth musculature, are essential for transmission of signals from enteric neurons to gastrointestinal smooth muscle cells. Interstitial cells of Cajal, therefore, integrate excitatory and inhibitory neurotransmission with slow-wave activity to orchestrate peristaltic motor activity of the gut. Impairment of the function of interstitial cells of Cajal causes severe gastrointestinal motor disorders. The results of our study show at the genetic level that these disorders are not only due to loss of slow-wave activity but also due to disturbed neurotransmission. Interstitial cells of Cajal generate rhythmic pacemaker currents, which result in rhythmic bowel contractions. Klein and colleagues use knock-in mutations to inactivate these cells in mice and find that they modulate bowel contractions by integrating excitatory and inhibitory neurotransmission in the gut.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms2626