A myogenic motor pattern in mice lacking myenteric interstitial cells of Cajal explained by a second coupled oscillator network

The interstitial cells of Cajal associated with the myenteric plexus (ICC-MP) are a network of coupled oscillators in the small intestine that generate rhythmic electrical phase waves leading to corresponding waves of contraction, yet rhythmic action potentials and intercellular calcium waves have b...

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Veröffentlicht in:American journal of physiology: Gastrointestinal and liver physiology 2020-02, Vol.318 (2), p.G225-G243
Hauptverfasser: Parsons, Sean P, Huizinga, Jan D
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Huizinga, Jan D
description The interstitial cells of Cajal associated with the myenteric plexus (ICC-MP) are a network of coupled oscillators in the small intestine that generate rhythmic electrical phase waves leading to corresponding waves of contraction, yet rhythmic action potentials and intercellular calcium waves have been recorded from c-kit-mutant mice that lack the ICC-MP, suggesting that there may be a second pacemaker network. The gap junction blocker carbenoxolone induced a "pinstripe" motor pattern consisting of rhythmic "stripes" of contraction that appeared simultaneously across the intestine with a period of ~4 s. The infinite velocity of these stripes suggested they were generated by a coupled oscillator network, which we call X. In c-kit mutants rhythmic contraction waves with the period of X traveled the length of the intestine, before the induction of the pinstripe pattern by carbenoxolone. Thus X is not the ICC-MP and appears to operate under physiological conditions, a fact that could explain the viability of these mice. Individual stripes consisted of a complex pattern of bands of contraction and distension, and between stripes there could be slide waves and v waves of contraction. We hypothesized that these phenomena result from an interaction between X and the circular muscle that acts as a damped oscillator. A mathematical model of two chains of coupled Fitzhugh-Nagumo systems, representing X and circular muscle, supported this hypothesis. The presence of a second coupled oscillator network in the small intestine underlines the complexity of motor pattern generation in the gut. Physiological experiments and a mathematical model indicate a coupled oscillator network in the small intestine in addition to the c-kit-expressing myenteric interstitial cells of Cajal. This network interacts with the circular muscle, which itself acts as a system of damped oscillators, to generate physiological contraction waves in c-kit (W) mutant mice.
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The gap junction blocker carbenoxolone induced a "pinstripe" motor pattern consisting of rhythmic "stripes" of contraction that appeared simultaneously across the intestine with a period of ~4 s. The infinite velocity of these stripes suggested they were generated by a coupled oscillator network, which we call X. In c-kit mutants rhythmic contraction waves with the period of X traveled the length of the intestine, before the induction of the pinstripe pattern by carbenoxolone. Thus X is not the ICC-MP and appears to operate under physiological conditions, a fact that could explain the viability of these mice. Individual stripes consisted of a complex pattern of bands of contraction and distension, and between stripes there could be slide waves and v waves of contraction. We hypothesized that these phenomena result from an interaction between X and the circular muscle that acts as a damped oscillator. A mathematical model of two chains of coupled Fitzhugh-Nagumo systems, representing X and circular muscle, supported this hypothesis. The presence of a second coupled oscillator network in the small intestine underlines the complexity of motor pattern generation in the gut. Physiological experiments and a mathematical model indicate a coupled oscillator network in the small intestine in addition to the c-kit-expressing myenteric interstitial cells of Cajal. 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This network interacts with the circular muscle, which itself acts as a system of damped oscillators, to generate physiological contraction waves in c-kit (W) mutant mice.</description><subject>Action Potentials - physiology</subject><subject>Animals</subject><subject>c-Kit protein</subject><subject>Calcium Signaling - physiology</subject><subject>Calcium signalling</subject><subject>Carbenoxolone - pharmacology</subject><subject>Colon</subject><subject>Contraction</subject><subject>Distension</subject><subject>Enteric nervous system</subject><subject>Female</subject><subject>Gastrointestinal Motility - physiology</subject><subject>Interstitial cells</subject><subject>Interstitial cells of Cajal</subject><subject>Interstitial Cells of Cajal - physiology</subject><subject>Intestine, Small - physiology</subject><subject>Mathematical models</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Models, Neurological</subject><subject>Models, Theoretical</subject><subject>Muscle Contraction</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>Mutants</subject><subject>Mutation</subject><subject>Myenteric plexus</subject><subject>Myenteric Plexus - physiology</subject><subject>Nerve Net - physiology</subject><subject>Neuromuscular Junction</subject><subject>Oscillators</subject><subject>Proto-Oncogene Proteins c-kit - genetics</subject><subject>Rhythms</subject><subject>Small intestine</subject><issn>0193-1857</issn><issn>1522-1547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1v1DAQhi0EokvhzglZ4tJLtp7EJskFqVqVD6lSL3C2HHu8eOvYwU4Ke-Kv47SlAi4eeeaZ8bx-CXkNbAsg6nN1mPZuy1gDsK0Z9E_IpqTrCgRvn5JNyTQVdKI9IS9yPjDGRA3wnJw00EFTN2JDfl3Q8Rj3GJymY5xjopOaZ0yBukBHp5F6pW9c2BcMQykUzq0xz252ylON3mcaLd2pQ7niz8krF9DQ4UgVzahjMFTHZfIlF7N23qv1mYDzj5huXpJnVvmMrx7iKfn64fLL7lN1df3x8-7iqtK8Z3PVWcO56C3oGrQwaLVRyjLU2qBig2ICOt6ZgQnOmQWwusdydkNB0fSsOSXv7-dOyzCi0UVLUl5OyY0qHWVUTv5bCe6b3Mdb2ZY_Ey2UAWcPA1L8vmCe5ejyKl4FjEuWdVPXHWtF0xf07X_oIS4pFHmF4u8EABfrRuye0inmnNA-LgNMru7KO3flnbtydbe0vPlbxGPDHzub30yZpaY</recordid><startdate>20200201</startdate><enddate>20200201</enddate><creator>Parsons, Sean P</creator><creator>Huizinga, Jan D</creator><general>American Physiological Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8016-1055</orcidid></search><sort><creationdate>20200201</creationdate><title>A myogenic motor pattern in mice lacking myenteric interstitial cells of Cajal explained by a second coupled oscillator network</title><author>Parsons, Sean P ; 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The gap junction blocker carbenoxolone induced a "pinstripe" motor pattern consisting of rhythmic "stripes" of contraction that appeared simultaneously across the intestine with a period of ~4 s. The infinite velocity of these stripes suggested they were generated by a coupled oscillator network, which we call X. In c-kit mutants rhythmic contraction waves with the period of X traveled the length of the intestine, before the induction of the pinstripe pattern by carbenoxolone. Thus X is not the ICC-MP and appears to operate under physiological conditions, a fact that could explain the viability of these mice. Individual stripes consisted of a complex pattern of bands of contraction and distension, and between stripes there could be slide waves and v waves of contraction. We hypothesized that these phenomena result from an interaction between X and the circular muscle that acts as a damped oscillator. A mathematical model of two chains of coupled Fitzhugh-Nagumo systems, representing X and circular muscle, supported this hypothesis. The presence of a second coupled oscillator network in the small intestine underlines the complexity of motor pattern generation in the gut. Physiological experiments and a mathematical model indicate a coupled oscillator network in the small intestine in addition to the c-kit-expressing myenteric interstitial cells of Cajal. This network interacts with the circular muscle, which itself acts as a system of damped oscillators, to generate physiological contraction waves in c-kit (W) mutant mice.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>31813235</pmid><doi>10.1152/ajpgi.00311.2019</doi><orcidid>https://orcid.org/0000-0001-8016-1055</orcidid><oa>free_for_read</oa></addata></record>
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subjects Action Potentials - physiology
Animals
c-Kit protein
Calcium Signaling - physiology
Calcium signalling
Carbenoxolone - pharmacology
Colon
Contraction
Distension
Enteric nervous system
Female
Gastrointestinal Motility - physiology
Interstitial cells
Interstitial cells of Cajal
Interstitial Cells of Cajal - physiology
Intestine, Small - physiology
Mathematical models
Mice
Mice, Inbred C57BL
Models, Neurological
Models, Theoretical
Muscle Contraction
Muscle, Smooth, Vascular - drug effects
Mutants
Mutation
Myenteric plexus
Myenteric Plexus - physiology
Nerve Net - physiology
Neuromuscular Junction
Oscillators
Proto-Oncogene Proteins c-kit - genetics
Rhythms
Small intestine
title A myogenic motor pattern in mice lacking myenteric interstitial cells of Cajal explained by a second coupled oscillator network
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