Literature DB >> 9409486

Development of electrical rhythmicity in the murine gastrointestinal tract is specifically encoded in the tunica muscularis.

S M Ward1, S C Harney, J R Bayguinov, G J McLaren, K M Sanders.   

Abstract

1. Interstitial cells of Cajal (ICCs) have been identified as pacemaker cells in the gastrointestinal (GI) tracts of vertebrates. We have studied the development of ICCs in pacemaker regions and the onset of electrical rhythmicity in the gastric antrum, small bowel and proximal colon of the mouse. 2. ICCs, as detected by c-Kit immunofluorescence, were found during embryogenesis in regions of the GI tract that eventually become pacemaker areas. Prior to birth, these cells were organized into well-structured networks, and by the end of the embryonic period the morphology of ICC networks in pacemaker regions appeared very similar to that observed in adult animals. 3. Electrical rhythmicity was recorded prior to birth (by E18) in the proximal GI tract (stomach and jejunum), and this activity developed to adult-like behaviour within a week after birth. In the ileum and proximal colon rhythmicity developed after birth, and adult-like characteristics were apparent within the first week. 4. Post-junctional responses of smooth muscles to neural inputs could be recorded at birth, and stimulation of intrinsic nerves often led to oscillatory activity resembling slow waves for up to several minutes following brief stimuli. Nerve stimulation augmented spontaneous activity in the proximal portions of the GI tract and elicited rhythmic activity temporarily in quiescent tissues of the distal GI tract. 5. ICCs and rhythmicity developed in an apparently normal manner in tissues isolated at birth and placed in organ culture. These data suggest that the tunica muscularis provides a suitable microenvironment for the development of ICCs and rhythmicity without the need for extrinsic stimuli. 6. Treatment of small intestinal tissues taken from embryos at E15 with neutralizing c-Kit antibodies abolished ICC development and the organization of ICCs into networks that typically occurs during the late embryonic period. Treatment of muscles taken from newborn animals with c-Kit antibodies blocked postnatal development of ICCs, disrupted already established and functional ICC networks, and rendered muscles electrically quiescent. 7. In summary, ICC networks develop in the pacemaker regions of the murine GI tract before birth. Development and organization of ICCs of the myenteric plexus region into networks precedes the development of electrical rhythmicity. Post-natal development of electrical rhythmicity is mainly characterized by enhancement of the amplitude and frequency of slow waves. The development of ICCs and electrical rhythmicity persists in vitro. ICCs appear to be necessary for the initiation of electrical rhythmicity. These findings provide further evidence for the pacemaker role of ICCs.

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Year:  1997        PMID: 9409486      PMCID: PMC1160108          DOI: 10.1111/j.1469-7793.1997.241bc.x

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  33 in total

1.  Spontaneous electrical activity of interstitial cells of Cajal isolated from canine proximal colon.

Authors:  P Langton; S M Ward; A Carl; M A Norell; K M Sanders
Journal:  Proc Natl Acad Sci U S A       Date:  1989-09       Impact factor: 11.205

2.  Neurogenic slow depolarizations and rapid oscillations in the membrane potential of circular muscle of mouse colon.

Authors:  R A Bywater; R C Small; G S Taylor
Journal:  J Physiol       Date:  1989-06       Impact factor: 5.182

3.  Electrophysiology of smooth muscle of the small intestine of some mammals.

Authors:  Y Hara; M Kubota; J H Szurszewski
Journal:  J Physiol       Date:  1986-03       Impact factor: 5.182

4.  Cytodifferentiation of the interstitial cells of Cajal related to the myenteric plexus of mouse intestinal muscle coat. An E.M. study from foetal to adult life.

Authors:  M S Faussone-Pellegrini
Journal:  Anat Embryol (Berl)       Date:  1985

5.  Boundary cells between longitudinal and circular layers: essential for electrical slow waves in cat intestine.

Authors:  N Suzuki; C L Prosser; V Dahms
Journal:  Am J Physiol       Date:  1986-03

6.  Interaction of two electrical pacemakers in muscularis of canine proximal colon.

Authors:  T K Smith; J B Reed; K M Sanders
Journal:  Am J Physiol       Date:  1987-03

7.  Origin and propagation of electrical slow waves in circular muscle of canine proximal colon.

Authors:  T K Smith; J B Reed; K M Sanders
Journal:  Am J Physiol       Date:  1987-02

8.  Neuromuscular structures in opossum esophagus: role of interstitial cells of Cajal.

Authors:  E E Daniel; V Posey-Daniel
Journal:  Am J Physiol       Date:  1984-03

9.  Development of c-Kit-positive cells and the onset of electrical rhythmicity in murine small intestine.

Authors:  S Torihashi; S M Ward; K M Sanders
Journal:  Gastroenterology       Date:  1997-01       Impact factor: 22.682

10.  The muscle coat of the lower esophageal sphincter in patients with achalasia and hypertensive sphincter. An electron microscopic study.

Authors:  M S Faussone-Pellegrini; C Cortesini
Journal:  J Submicrosc Cytol       Date:  1985-10
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  39 in total

1.  Interstitial cells of cajal generate electrical slow waves in the murine stomach.

Authors:  T Ordög; S M Ward; K M Sanders
Journal:  J Physiol       Date:  1999-07-01       Impact factor: 5.182

Review 2.  Interstitial cells of Cajal in enteric neurotransmission.

Authors:  S M Ward
Journal:  Gut       Date:  2000-12       Impact factor: 23.059

3.  Generation of slow waves in the antral region of guinea-pig stomach--a stochastic process.

Authors:  G D Hirst; F R Edwards
Journal:  J Physiol       Date:  2001-08-15       Impact factor: 5.182

4.  Simultaneous imaging of Ca2+ signals in interstitial cells of Cajal and longitudinal smooth muscle cells during rhythmic activity in mouse ileum.

Authors:  Toshiko Yamazawa; Masamitsu Iino
Journal:  J Physiol       Date:  2002-02-01       Impact factor: 5.182

5.  The development and distribution of the interstitial cells of Cajal in the intestine of the equine fetus and neonate.

Authors:  C Fintl; G T Pearson; S W Ricketts; I G Mayhew; N P H Hudson
Journal:  J Anat       Date:  2004-07       Impact factor: 2.610

6.  The enteric nervous system is not essential for the propulsion of gut contents in fetal mice.

Authors:  R B Anderson; H Enomoto; J C Bornstein; H M Young
Journal:  Gut       Date:  2004-10       Impact factor: 23.059

7.  Role of PI3-kinase in the development of interstitial cells and pacemaking in murine gastrointestinal smooth muscle.

Authors:  S M Ward; M F Brennan; V M Jackson; K M Sanders
Journal:  J Physiol       Date:  1999-05-01       Impact factor: 5.182

8.  In vivo gastric and intestinal slow waves in W/WV mice.

Authors:  Xiaohua Hou; Jieyun Yin; Jinsong Liu; Pankaj J Pasricha; J D Z Chen
Journal:  Dig Dis Sci       Date:  2005-07       Impact factor: 3.199

9.  Loss of interstitial cells of Cajal network in severe idiopathic gastroparesis.

Authors:  Edda Battaglia; Gabrio Bassotti; Graziella Bellone; Luca Dughera; Anna-Maria Serra; Luigi Chiusa; Alessandro Repici; Pierroberto Mioli; Giorgio Emanuelli
Journal:  World J Gastroenterol       Date:  2006-10-14       Impact factor: 5.742

10.  Ano1, a Ca2+-activated Cl- channel, coordinates contractility in mouse intestine by Ca2+ transient coordination between interstitial cells of Cajal.

Authors:  Raman Deep Singh; Simon J Gibbons; Siva Arumugam Saravanaperumal; Peng Du; Grant W Hennig; Seth T Eisenman; Amelia Mazzone; Yujiro Hayashi; Chike Cao; Gary J Stoltz; Tamas Ordog; Jason R Rock; Brian D Harfe; Joseph H Szurszewski; Gianrico Farrugia
Journal:  J Physiol       Date:  2014-07-25       Impact factor: 5.182

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