Table 1.
Type of Cell and Anatomical Localization | Common Name(s) | Proposed Function(s) | Representative References |
---|---|---|---|
Myenteric ICC (in region between circular and longitudinal muscle layers) | ICC-MY; ICC-MP | 1) Pacemaker cells that generate electrical slow waves; 2) form networks that allow active (regenerative) propagation of slow waves; 3) voltage-dependent excitability due to expression of voltage-dependent Ca2+ channels; 4) role in setting resting membrane potential and basal excitability of SIP syncytium | 7, 19, 44, 83, 99, 107, 113, 123 |
Intramuscular ICC (within bundles of smooth muscle cells and lying in close proximity to nerve varicosities) | ICC-IM; ICC-DMP in region of the deep muscular plexus of the small intestine | 1) Transduction of neurotransmitter signals from enteric motor neurons; 2) mechano-sensitivity; 3) lack of voltage-dependent excitability due to generally low expression of voltage-dependent Ca2+ currents; 4) contribution to active propagation in gastric muscles; 5) mediation of inflammatory input via protease-activated receptors | 8, 10, 14, 18, 33, 76, 104, 106, 112, 114 |
ICC within septa between bundles of muscle | ICC-SEP | 1) Active propagation of slow waves into the depth of thicker muscles (as in human GI tract); 2) interactions with enteric neurons | 42, 74, 115 |
ICC along the submucosal surface of the circular muscle layer in colon and to small extent in stomach | ICC-SM | 1) Pacemaker activity in the colon | 11, 100 |
ICC at the serosal surface of the longitudinal muscle layer | ICC-SS | Unknown | 2, 13 |
Fibroblast-like cells found in all regions of the GI tract; generally common localization with ICC; also in close apposition with varicosities of enteric neurons | *PDGFRα+ cells | 1) Mediation of purinergic inhibition (purinergic inhibitory junction potential); 2) mediation of inflammatory input via protease-activated receptors | 5, 47, 69–71, 104 |
Smooth muscle cells | Circular SMCs, longitudinal SMCs, sphincteric SMCs, sling SMCs in stomach | 1) Generation of forces in motility; 2) maintenance of sphincter tone; 3) contributions to setting resting excitability of SIP syncytium; 4) transduction of neural and hormonal responses; 5) mediation of Ca2+ sensitization mechanisms | 32, 54, 75, 84, 91, 101, 103, 117 |
PDGFRα+ cells also have distinct localization and cellular morphologies when found within muscle bundles or in the myenteric region. They are often intertwined with ICC in these localizations. At present, no differences in cells within muscle bundles and cells in the myenteric region have been distinguished; thus, for the purposes of this overview description, these cells are not broken down into
PDGFRα+-MY and
PDGFRα+-IM classes.