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Methods to Study Epithelial Transport Protein Function and Expression in Native Intestine and Caco-2 Cells Grown in 3D
Published on: March 16, 2017
Membrane currents in cultured human intestinal smooth muscle cells
A V Zholos1, C J Fenech, S A Prestwich
1Department of Pharmacology and Clinical Pharmacology, St George's Hospital Medical School, London SW17 ORE, UK.
Insights
This study identified two novel Ca2+-blockable cationic currents, I(HA) and I(DA), in human intestinal smooth muscle cells. These currents exhibit distinct ion selectivity and voltage-dependent properties, offering new insights into intestinal smooth muscle electrophysiology.
Area of Science:
- Cellular Electrophysiology
- Ion Channel Physiology
- Gastrointestinal Physiology
Background:
- Human intestinal smooth muscle (HISM) cells possess complex electrical properties crucial for function.
- Understanding voltage-gated ion currents in HISM is essential for elucidating smooth muscle contractility and dysfunction.
Purpose of the Study:
- To characterize voltage-gated ion currents in cultured HISM cells.
- To identify the ion selectivity and pharmacological properties of these currents.
- To investigate the role of calcium and other modulators on identified currents.
Main Methods:
- Whole-cell patch-clamp recordings were employed on cultured HISM cells.
- Ion currents were analyzed under various ionic conditions and in the presence of specific channel blockers.
- Pharmacological agents including tetraethylammonium, iberiotoxin, tetrodotoxin, SK&F 96365, Gd3+, La3+, and carbachol were utilized.
Main Results:
- A tetraethylammonium-sensitive K+ current and a tetrodotoxin-sensitive Na+ current were identified.
- Two novel Ca2+-blockable cationic currents, I(HA) and I(DA), were discovered in divalent cation-free solutions.
- I(HA) and I(DA) displayed distinct ion selectivity (K+ > Cs+ > Na+ for I(HA); Na+ > K+ >> Cs+ for I(DA)) and voltage-dependent properties.
- I(DA) showed unique voltage-dependent activation and inactivation, while I(HA) exhibited instantaneous activation and no inactivation.
- Carbachol modulated both currents, increasing I(HA) and abolishing I(DA).
Conclusions:
- HISM cells express distinct voltage-gated K+, Na+, and novel cationic currents.
- I(HA) and I(DA) are Ca2+-blockable cationic currents carried by different channels with unique properties.
- I(DA) presents novel voltage-dependent characteristics for a cationic current, warranting further investigation into its channel composition and function.
Abstract:
Using whole-cell patch-clamp recording techniques, we have examined voltage-gated ion currents in a cultured human intestinal smooth muscle cell line (HISM). Experiments were performed at room temperature on cells after passages 16 and 17. Two major components of the whole-cell current were a tetraethylammonium-sensitive (IC50 = 9 mM), iberiotoxin-resistant, delayed rectifier K+ current and a Na+ current inhibited by tetrodotoxin (IC50 A 100 nM). No measurable inward current via voltage-gated Ca2+ channels could be detected in these cells even with 10 mM Ca2+ or Ba2+ in the external solution. No current attributable to calcium-activated K+ channels was found and no cationic current in response to muscarinic receptor activation was present. In divalent cation-free external solution two additional currents were activated: an inwardly rectifying hyperpolarization-activated current, I(HA), and a depolarization-activated current, I(DA) x I(HA) and I(DA) could be carried by several monovalent cations; the sizes of currents in descending order were: K+ > Cs+ > Na+ for I(HA) and Na+ > K+ >> Cs+ for I(DA). I(HA) was activated and deactivated instantaneously and showed no inactivation whereas I(DA) was activated, inactivated and deactivated within tens of milliseconds. These currents were inhibited by external calcium with an IC50 of 0.3 microM for I(DA) and an IC50 of 20 microM for I(HA). Cyclopiazonic acid (CPA) induced an outward, but not an inward current. SK&F 96365, a blocker of store-operated Ca2+ channels, suppressed I(DA) with a half-maximal inhibitory concentration of 9 microM but was ineffective in inhibiting I(HA) at concentrations up to 100 microM. Gd3+ and La3+ strongly suppressed I(DA) at 1 and 10 microM, respectively and were less effective in blocking I(HA) (complete inhibition required a concentration of 100 microM for both). Carbachol at 10-100 microM evoked about a 3-fold increase in I(HA) amplitude and completely abolished I(DA). We conclude that I(HA) and I(DA) are Ca2+-blockable cationic currents with different ion selectivity profiles that are carried by different channels. I(DA) shows novel voltage-dependent properties for a cationic current.
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