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Published on: December 21, 2010
A large, multiple-conductance chloride channel in normal human T lymphocytes
L C Schlichter1, R Grygorczyk, P A Pahapill
1Department of Physiology, University of Toronto, Ontario, Canada.
Insights
Researchers identified a large conductance chloride channel in human T lymphocytes, crucial for cell function. This channel exhibits voltage-dependent gating and selective ion permeability, offering new insights into lymphocyte physiology.
Area of Science:
- Ion channel biophysics
- Human lymphocyte physiology
- Cellular transport mechanisms
Background:
- Chloride (Cl) channels are implicated in lymphocyte functions like volume regulation and cytotoxicity.
- Direct characterization of these channels in normal human lymphocytes is limited.
Purpose of the Study:
- To describe a large conductance Cl channel in normal human peripheral T lymphocytes.
- To characterize its biophysical properties, including conductance, voltage dependence, and ion selectivity.
Main Methods:
- Utilized excised, inside-out patch-clamp electrophysiology on normal human peripheral T lymphocytes.
- Analyzed single-channel currents to determine conductance, voltage dependence, and ion selectivity.
Main Results:
- Identified a large conductance Cl channel (approx. 365 pS) in ~50% of T lymphocyte patches.
- The channel displays voltage-dependent gating, with maximal opening probability between -15 mV and +15 mV.
- Demonstrated high selectivity for Cl- over Na+ and K+ (approx. 30:1) and characterized anion selectivity sequence.
Conclusions:
- A novel, large conductance Cl channel exists in human T lymphocytes.
- This channel's properties suggest a significant role in lymphocyte function.
- Further research is warranted to elucidate its specific physiological roles.
Abstract:
Chloride (Cl) channels have been proposed to play roles in lymphocyte functions including volume regulation and cellular cytotoxicity; however, direct studies of such channels in normal human lymphocytes are lacking. In the present study we describe a large conductance Cl channel observed in about 50% of excised, inside-out patches from normal human peripheral T lymphocytes. The channel has multiple conductance states with linear single-channel current-versus-voltage relationships in symmetrical Cl solutions. The most prevalent state is the largest, which has a conductance of about 365 pS. The channel closes in a voltage-dependent manner at both negative and positive potentials, but does not show voltage-dependent inactivation. The probability of opening is maximal between -15 mV and +15 mV and the voltage dependence is well described by two Boltzmann equations with half-maximal probabilities at -22.8 mV and +18.0 mV. The slopes of the voltage dependence suggest two gates in series with 5.7 and 9.6 equivalent charges. The channel was about 30 times more selective for Cl- than for Na+ or K+ under balanced osmolarity but less selective (approx. 11:1) under a large osmotic gradient. The single-channel conductance increased with Cl concentration with an apparent saturation at about 581 pS and a Michaelis-Menten constant of about 120 mM. The selectivity sequence among anions, determined from changes in reversal potential was: I- greater than NO3- greater than Br-, Cl- greater than F-, isethionate, HCO3- greater than SO4(2-) greater than gluconate, propionate greater than aspartate much greater than Na+, K+ and was apparently the same for subconductance states.(ABSTRACT TRUNCATED AT 250 WORDS)
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