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Ca 2+ signalling behaviours of intramuscular interstitial cells of Cajal in the murine colon
Author(s) -
Drumm Bernard T.,
Hwang Sung J.,
Baker Salah A.,
Ward Sean M.,
Sanders Kenton M.
Publication year - 2019
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jp278036
Subject(s) - interstitial cell of cajal , endoplasmic reticulum , depolarization , interstitial cell , chemistry , biophysics , motility , electrophysiology , calcium signaling , microbiology and biotechnology , biology , receptor , neuroscience , anatomy , endocrinology , biochemistry , smooth muscle
Key points Colonic intramuscular interstitial cells of Cajal (ICC‐IM) exhibit spontaneous Ca 2+ transients manifesting as stochastic events from multiple firing sites with propagating Ca 2+ waves occasionally observed. Firing of Ca 2+ transients in ICC‐IM is not coordinated with adjacent ICC‐IM in a field of view or even with events from other firing sites within a single cell. Ca 2+ transients, through activation of Ano1 channels and generation of inward current, cause net depolarization of colonic muscles. Ca 2+ transients in ICC‐IM rely on Ca 2+ release from the endoplasmic reticulum via IP 3 receptors, spatial amplification from RyRs and ongoing refilling of ER via the sarcoplasmic/endoplasmic‐reticulum‐Ca 2+ ‐ATPase. ICC‐IM are sustained by voltage‐independent Ca 2+ influx via store‐operated Ca 2+ entry. Some of the properties of Ca 2+ in ICC‐IM in the colon are similar to the behaviour of ICC located in the deep muscular plexus region of the small intestine, suggesting there are functional similarities between these classes of ICC.Abstract A component of the SIP syncytium that regulates smooth muscle excitability in the colon is the intramuscular class of interstitial cells of Cajal (ICC‐IM). All classes of ICC (including ICC‐IM) express Ca 2+ ‐activated Cl − channels, encoded by Ano1 , and rely upon this conductance for physiological functions. Thus, Ca 2+ handling in ICC is fundamental to colonic motility. We examined Ca 2+ handling mechanisms in ICC‐IM of murine proximal colon expressing GCaMP6f in ICC. Several Ca 2+ firing sites were detected in each cell. While individual sites displayed rhythmic Ca 2+ events, the overall pattern of Ca 2+ transients was stochastic. No correlation was found between discrete Ca 2+ firing sites in the same cell or in adjacent cells. Ca 2+ transients in some cells initiated Ca 2+ waves that spread along the cell at ∼100 µm s −1 . Ca 2+ transients were caused by release from intracellular stores, but depended strongly on store‐operated Ca 2+ entry mechanisms. ICC Ca 2+ transient firing regulated the resting membrane potential of colonic tissues as a specific Ano1 antagonist hyperpolarized colonic muscles by ∼10 mV. Ca 2+ transient firing was independent of membrane potential and not affected by blockade of L‐ or T‐type Ca 2+ channels. Mechanisms regulating Ca 2+ transients in the proximal colon displayed both similarities to and differences from the intramuscular type of ICC in the small intestine. Similarities and differences in Ca 2+ release patterns might determine how ICC respond to neurotransmission in these two regions of the gastrointestinal tract.