scholarly journals Slow wave propagation and plasticity of interstitial cells of Cajal in the small intestine of diabetic rats

2011 ◽  
Vol 96 (10) ◽  
pp. 1039-1048 ◽  
Author(s):  
Wim J. E. P. Lammers ◽  
H. M. Al-Bloushi ◽  
S. A. Al-Eisaei ◽  
F. A. Al-Dhaheri ◽  
B. Stephen ◽  
...  
2017 ◽  
Vol 312 (3) ◽  
pp. G228-G245 ◽  
Author(s):  
John Malysz ◽  
Simon J. Gibbons ◽  
Siva A. Saravanaperumal ◽  
Peng Du ◽  
Seth T. Eisenman ◽  
...  

Myenteric plexus interstitial cells of Cajal (ICC-MY) in the small intestine are Kit+ electrical pacemakers that express the Ano1/TMEM16A Ca2+-activated Cl– channel, whose functions in the gastrointestinal tract remain incompletely understood. In this study, an inducible Cre-LoxP-based approach was used to advance the understanding of Ano1 in ICC-MY of adult mouse small intestine. KitCreERT2/+;Ano1Fl/Fl mice were treated with tamoxifen or vehicle, and small intestines (mucosa free) were examined. Quantitative RT-PCR demonstrated ~50% reduction in Ano1 mRNA in intestines of conditional knockouts (cKOs) compared with vehicle-treated controls. Whole mount immunohistochemistry showed a mosaic/patchy pattern loss of Ano1 protein in ICC networks. Ca2+ transients in ICC-MY network of cKOs displayed reduced duration compared with highly synchronized controls and showed synchronized and desynchronized profiles. When matched, the rank order for Ano1 expression in Ca2+ signal imaged fields of view was as follows: vehicle controls>>>cKO(synchronized)>cKO(desynchronized). Maintenance of Ca2+ transients’ synchronicity despite high loss of Ano1 indicates a large functional reserve of Ano1 in the ICC-MY network. Slow waves in cKOs displayed reduced duration and increased inter-slow-wave interval and occurred in regular- and irregular-amplitude oscillating patterns. The latter activity suggested ongoing interaction by independent interacting oscillators. Lack of slow waves and depolarization, previously reported for neonatal constitutive knockouts, were also seen. In summary, Ano1 in adults regulates gastrointestinal function by determining Ca2+ transients and electrical activity depending on the level of Ano1 expression. Partial Ano1 loss results in Ca2+ transients and slow waves displaying reduced duration, while complete and widespread absence of Ano1 in ICC-MY causes lack of slow wave and desynchronized Ca2+ transients. NEW & NOTEWORTHY The Ca2+-activated Cl− channel, Ano1, in interstitial cells of Cajal (ICC) is necessary for normal gastrointestinal motility. We knocked out Ano1 to varying degrees in ICC of adult mice. Partial knockout of Ano1 shortened the widths of electrical slow waves and Ca2+ transients in myenteric ICC but Ca2+ transient synchronicity was preserved. Near-complete knockout was necessary for transient desynchronization and loss of slow waves, indicating a large functional reserve of Ano1 in ICC. View this article's corresponding video summary at https://youtu.be/cyPtDP0KLY4 .


Author(s):  
Maria-Gabriela Colmenares Aguilar ◽  
Amelia Mazzone ◽  
Seth T Eisenman ◽  
Peter R Strege ◽  
Cheryl E Bernard ◽  
...  

Interstitial cells of Cajal (ICC) generate electrical slow waves, which are required for normal gastrointestinal motility. The mechanisms for generation of normal pacemaking are not fully understood. Normal gastrointestinal contractility and electrical slow wave activity depend on the presence of extracellular HCO3-. Previous transcriptional analysis identified enrichment of mRNA encoding the electrogenic Na+/HCO3- cotransporter (NBCe1) gene (Slc4a4) in pacemaker myenteric ICC in mouse small intestine. We aimed to determine the distribution of NBCe1 protein in ICC of the mouse gastrointestinal tract, and to identify the transcripts of the Slc4a4 gene in mouse and human small intestinal tunica muscularis. We determined the distribution of NBCe1-immunoreactivity (NBCe1-IR) by immunofluorescent labeling in mouse and human tissues. In mice, NBCe1-IR was restricted to Kit-positive myenteric ICC of the stomach and small intestine and sub-muscular ICC of the large intestine; that is the slow wave generating subset of ICC. Other sub-types of ICC were NBCe1-negative. Quantitative real time PCR identified >500 fold enrichment of Slc4a4‑207 and Slc4a4‑208 transcripts (IP3-receptor binding protein released by IP3" (IRBIT) regulated isoforms) in Kit expressing cells isolated from KitcreERT2/+, Rpl22tm1.1Psam/Sj mice and from single GFP-positive ICC from Kittm1Rosay mice. Human jejunal tunica muscularis ICC were also NBCe1-positive and SLC4A4‑201 and SLC4A4‑204 RNAs were >300 fold enriched relative to SLC4A4‑202. In summary, NBCe1 protein expressed in ICC with electrical pacemaker function is encoded by Slc4a4 gene transcripts that generate IRBIT regulated isoforms of NBCe1. In conclusion Na+/HCO3- cotransport through NBCe1 contributes to the generation of pacemaker activity in subsets of ICC.


2005 ◽  
Vol 288 (1) ◽  
pp. G151-G158 ◽  
Author(s):  
Sylvain Bellier ◽  
Nelly R. Da Silva ◽  
Geneviève Aubin-Houzelstein ◽  
Colette Elbaz ◽  
Jean-Marie Vanderwinden ◽  
...  

The interstitial cells of Cajal (ICC) play an important role in coordinating intestinal motility, and structural alterations in ICC are found in several human digestive diseases. Mouse models with defects in ICC allow a better understanding of their functions. We investigated the pattern of intestinal motility and the distribution of ICC in the PRM/Alf inbred mouse strain, characterized by a selective intestinal lengthening. In PRM/Alf mice, the digestive transit time, evaluated by using thermophilic Bacillus subtilis spores, was normal, indicating accelerated transit. The contractility and slow-wave frequency, recorded on isolated segments from the proximal small intestine, were significantly increased. The number of ICC was also significantly higher along the small intestine and the colon. The concomitant increase of the contractility, the slow-wave frequency, and the number of ICC is consistent with the proposal of a role of ICC number increase in the higher intestinal transit speed. The PRM/Alf model should be useful to further investigate the roles of ICC in the control of digestive motility.


1990 ◽  
Vol 258 (6) ◽  
pp. G894-G903 ◽  
Author(s):  
J. L. Conklin ◽  
C. Du

Colonic slow waves (SWs) are generated by nonneuronal cells located at the interface of the submucosa and muscularis propria. It has been proposed that SWs arise from a complex of nerves, interstitial cells of Cajal, and smooth muscle found at this location. These experiments test the hypothesis that the propagation of colonic SWs depends on an intact interface between the submucosa and muscularis propria. The electromyogram was recorded from segments of the proximal colon of the cat. All intact tissues generated SWs that propagated in the long and circumferential axes of the colon. Tetrodotoxin did not disrupt SW propagation in either axis. Transection of tissues between recording sites interrupted the spread of SWs in both axes. Transection of the submucosa disrupted the longitudinal spread of SWs, whereas transection of the muscularis propria did not. Removing the submucosa from the midportion of tissue segments oriented in the long axis of the colon resulted in a loss of SWs from the segment devoid of submucosa. Transection of the submucosa of tissue segments oriented in the circular axis of the colon did not disrupt circumferential propagation of SWs. Dissecting a 1-cm-wide segment of submucosa from the midportion of such a circularly oriented tissue did not disrupt the circumferential spread of SWs, and SWs were recorded from the muscle segment that was devoid of submucosa. SWs were not recorded from the segment devoid of submucosa when it was isolated from adjacent intact segments. The data support the hypothesis that the regeneration of SWs during their longitudinal propagation takes place at the interface between the submucosa and muscularis propria.


2018 ◽  
Vol 54 (1) ◽  
pp. 63
Author(s):  
Il Koo Park ◽  
Jin Ho Kim ◽  
Chan Guk Park ◽  
Man Yoo Kim ◽  
Shankar Prasad Parajuli ◽  
...  

1991 ◽  
Vol 69 (8) ◽  
pp. 1133-1142 ◽  
Author(s):  
Jan D. Huizinga

Recent investigation of the ultrastracture and electrophysiology of gastrointestinal smooth muscle layers has revealed a fascinating heterogeneity in cell type, cell structure, intercellular communication, and generated electrical activities. Networks of interstitial cells of Cajal (ICC) have been identified in many muscle layers and evidence is accumulating for a role of these networks in gut pacemaking activity. Synchronized motility in the organs of the gut result from interaction between ICC, neural-tissue, and smooth muscle cells. Regulation of cell to cell communication between the different cell types will be an important area for further research. Progress has been made in the elucidation of the ionic basis of the slow wave type action potentials and the spike-like action potentials. The mechanism underlying smooth muscle autorhythmicity seems different from that encountered in cardiac tissue, and evidence exists for metabolic regulation of the frequency of slow wave type action potentials.Key words: pacemaker activity, slow wave, autorhythmicity, interstitial cells of Cajal.


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