Author
Listed:
- Sabine Klein
(Klinikum rechts der Isar, Technische Universität München)
- Barbara Seidler
(Klinikum rechts der Isar, Technische Universität München)
- Anna Kettenberger
(Klinikum rechts der Isar, Technische Universität München)
- Andrei Sibaev
(Ludwig-Maximilians-Universität München)
- Michael Rohn
(Lehrstuhl für Humanbiologie, Technische Universität München)
- Robert Feil
(Interfaculty Institute of Biochemistry, University of Tübingen)
- Hans-Dieter Allescher
(Zentrum für Innere Medizin, Klinikum Garmisch-Partenkirchen)
- Jean-Marie Vanderwinden
(Université Libre de Bruxelles (ULB), ULB Neuroscience Institute (UNI), Neurophysiology lab)
- Franz Hofmann
(Forschergruppe 923, Institut für Pharmakologie und Toxikologie, Klinikum rechts der Isar, Technische Universität München)
- Michael Schemann
(Lehrstuhl für Humanbiologie, Technische Universität München)
- Roland Rad
(Wellcome Trust Sanger Institute, Genome Campus)
- Martin A. Storr
(Ludwig-Maximilians-Universität München)
- Roland M. Schmid
(Klinikum rechts der Isar, Technische Universität München)
- Günter Schneider
(Klinikum rechts der Isar, Technische Universität München)
- Dieter Saur
(Klinikum rechts der Isar, Technische Universität München)
Abstract
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-KitCreERT2 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.
Suggested Citation
Sabine Klein & Barbara Seidler & Anna Kettenberger & Andrei Sibaev & Michael Rohn & Robert Feil & Hans-Dieter Allescher & Jean-Marie Vanderwinden & Franz Hofmann & Michael Schemann & Roland Rad & Mart, 2013.
"Interstitial cells of Cajal integrate excitatory and inhibitory neurotransmission with intestinal slow-wave activity,"
Nature Communications, Nature, vol. 4(1), pages 1-9, June.
Handle:
RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms2626
DOI: 10.1038/ncomms2626
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