» Articles » PMID: 7273110

Gap Junctions of the Muscles of the Small and Large Intestine

Overview
Journal Cell Tissue Res
Date 1981 Jan 1
PMID 7273110
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

The distribution of gap junctions (nexuses) in various parts of the small and large intestines of the guinea-pig was studied using the freeze-fracture technique and in thin sections. The percentage area of smooth muscle cell surface occupied by gap junctions varies from 0.50% in the circular muscle of the duodenum to zero in the longitudinal muscle of the ileum. In the circular muscle of the jejunum and ileum the area occupied by nexuses is 0.22% (or about 11 micrometers 2 per cell). The sizes of junctions range from less than 0.01 micrometer 2 to 0.20 micrometer 2, with two-thirds of them being smaller than 0.05 micrometer 2. In the colon, gap junctions are rare, very small and confined to the circular muscle layer. Even the smallest aggregates of intramembrane particles correspond to areas of close apposition between the membranes of adjacent cells; it is therefore justified to interpret them as being gap junctions. Some gap junctions are formed between a smooth muscle cell and an interstitial cell. Gap junctions are not found in the longitudinal muscle of the small intestine; this is in sharp contrast to the abundance of gap junctions in the adjacent circular layer. In the small intestine of cats and rabbits, gap junctions are abundant in the circular muscle layer, whereas they are very small in size and very few in number in the longitudinal muscle layer.

Citing Articles

Review and Study of Uterine Bioelectrical Waveforms and Vector Analysis to Identify Electrical and Mechanosensitive Transduction Control Mechanisms During Labor in Pregnant Patients.

Garfield R, Murphy L, Gray K, Towe B Reprod Sci. 2020; 28(3):838-856.

PMID: 33090378 DOI: 10.1007/s43032-020-00358-5.


Diabetes-induced mechanophysiological changes in the small intestine and colon.

Zhao M, Liao D, Zhao J World J Diabetes. 2017; 8(6):249-269.

PMID: 28694926 PMC: 5483424. DOI: 10.4239/wjd.v8.i6.249.


Gap junctions are non-randomly distributed inDrosophila wing discs.

Ryerse J Wilehm Roux Arch Dev Biol. 2017; 191(5):335-339.

PMID: 28305287 DOI: 10.1007/BF00848494.


Functional alterations in gut contractility after connexin36 ablation and evidence for gap junctions forming electrical synapses between nitrergic enteric neurons.

Nagy J, Urena-Ramirez V, Ghia J FEBS Lett. 2014; 588(8):1480-90.

PMID: 24548563 PMC: 4043341. DOI: 10.1016/j.febslet.2014.02.002.


Regulation of gastrointestinal motility--insights from smooth muscle biology.

Sanders K, Koh S, Ro S, Ward S Nat Rev Gastroenterol Hepatol. 2012; 9(11):633-45.

PMID: 22965426 PMC: 4793911. DOI: 10.1038/nrgastro.2012.168.


References
1.
Chalcroft J, Bullivant S . An interpretation of liver cell membrane and junction structure based on observation of freeze-fracture replicas of both sides of the fracture. J Cell Biol. 1970; 47(1):49-60. PMC: 2108397. DOI: 10.1083/jcb.47.1.49. View

2.
Gabella G . Intercellular junctions between circular and longitudinal intestinal muscle layers. Z Zellforsch Mikrosk Anat. 1972; 125(2):191-9. DOI: 10.1007/BF00306788. View

3.
Fry G, Devine C, Burnstock G . Freeze-fracture studies of nexuses between smooth muscle cells. Close relationship to sarcoplasmic reticulum. J Cell Biol. 1977; 72(1):26-34. PMC: 2110984. DOI: 10.1083/jcb.72.1.26. View

4.
Cobb J, Bennett T . A study of intercellular relationships in developing and mature visceral smooth muscle. Z Zellforsch Mikrosk Anat. 1969; 100(4):516-26. DOI: 10.1007/BF00344372. View

5.
Friend D, Gilula N . Variations in tight and gap junctions in mammalian tissues. J Cell Biol. 1972; 53(3):758-76. PMC: 2108762. DOI: 10.1083/jcb.53.3.758. View