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Open AccessJournal ArticleDOI

A Ca2+-activated Cl− conductance in interstitial cells of Cajal linked to slow wave currents and pacemaker activity

TLDR
A role for a Ca2+‐activated Cl− conductance in slow wave current in ICC is demonstrated and is consistent with the idea that ANO1 participates in pacemaker activity.
Abstract
Interstitial cells of Cajal (ICC) are unique cells that generate electrical pacemaker activity in gastrointestinal (GI) muscles. Many previous studies have attempted to characterize the conductances responsible for pacemaker current and slow waves in the GI tract, but the precise mechanism of electrical rhythmicity is still debated. We used a new transgenic mouse with a bright green fluorescent protein (copGFP) constitutively expressed in ICC to facilitate study of these cells in mixed cell dispersions. We found that ICC express a specialized ‘slow wave’ current. Reversal of tail current analysis showed this current was due to a Cl− selective conductance. ICC express ANO1, a Ca2+-activated Cl− channel. Slow wave currents are not voltage dependent, but a secondary voltage-dependent process underlies activation of these currents. Removal of extracellular Ca2+, replacement of Ca2+ with Ba2+, or extracellular Ni2+ (30 μm) blocked the slow wave current. Single Ca2+-activated Cl− channels with a unitary conductance of 7.8 pS were resolved in excised patches of ICC. These are similar in conductance to ANO1 channels (8 pS) expressed in HEK293 cells. Slow wave current was blocked in a concentration-dependent manner by niflumic acid (IC50= 4.8 μm). Slow wave currents are associated with transient depolarizations of ICC in current clamp, and these events were blocked by niflumic acid. These findings demonstrate a role for a Ca2+-activated Cl− conductance in slow wave current in ICC and are consistent with the idea that ANO1 participates in pacemaker activity.

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Structure and Function of TMEM16 Proteins (Anoctamins)

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Journal ArticleDOI

Expression of anoctamin 1/TMEM16A by interstitial cells of Cajal is fundamental for slow wave activity in gastrointestinal muscles

TL;DR: The fundamental role of ANO1 is demonstrated in the generation of slow waves in GI ICC, which failed to develop by birth in mice homozygous for a null allele of Tmem16a and did not develop subsequent to birth in organ culture, as in wildtype and heterozygous muscles.
Journal ArticleDOI

Interstitial Cells: Regulators of Smooth Muscle Function

TL;DR: Structural, functional, and molecular features of interstitial cells are described and their contributions in determining the behaviors of smooth muscle tissues are discussed.
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Regulation of gastrointestinal motility—insights from smooth muscle biology

TL;DR: The cells and mechanisms that generate smooth muscle contractile behaviour and gastrointestinal motility are provided and patterns of contractile activity are determined by inputs from enteric motor neurons that innervate smooth muscle cells and interstitial cells.
References
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Journal ArticleDOI

W/kit gene required for interstitial cells of Cajal and for intestinal pacemaker activity

TL;DR: It is shown that the interstitial cells of Cajal express the Kit receptor tyrosine kinase, and mice with mutations in the dominant white spotting locus, which have cellular defects in haematopoiesis, melanogenesis and gametogenesis, also lack the network of intestitial cells ofCajal associated with Auerbach's nerve plexus and intestinal pacemaker activity.
Journal ArticleDOI

TMEM16A confers receptor-activated calcium-dependent chloride conductance

TL;DR: It is shown that transmembrane protein 16A (TMEM16A), which is also called anoctamin 1 (ANO1), is a bona fide Ca2+-activated chloride channel that is activated by intracellular Ca2- and Ca2+, and defines a new family of ionic channels.
Journal ArticleDOI

TMEM16A, A Membrane Protein Associated with Calcium-Dependent Chloride Channel Activity

TL;DR: Identification of a previously unknown family of membrane proteins associated with chloride channel function will improve the understanding of chloride transport physiopathology and allow for the development of pharmacological tools useful for basic research and drug development.
Journal ArticleDOI

Expression cloning of TMEM16A as a calcium-activated chloride channel subunit.

TL;DR: Using Axolotl oocytes as an expression system, TMEM16A is identified as the Xenopus oocyte CaCC and may help the development of CaCC modulators for treating diseases including hypertension and cystic fibrosis.
Journal ArticleDOI

Mutation of the proto‐oncogene c‐kit blocks development of interstitial cells and electrical rhythmicity in murine intestine.

TL;DR: The characteristics and distribution of ICs and electrical activity of small intestinal muscles from mice with mutations at the dominant‐white spotting/c‐kit (W) locus are studied to show that neural regulation of gastrointestinal muscles can develop independently of the IC network.
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