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The Volume Activated Potassium Channel KCNK5 is Up-Regulated in Activated Human T Cells, but Volume Regulation is Impaired.
- Source :
-
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology [Cell Physiol Biochem] 2016; Vol. 38 (3), pp. 883-92. Date of Electronic Publication: 2016 Feb 25. - Publication Year :
- 2016
-
Abstract
- Background/aims: The potential role of the two-pore domain potassium channel KCNK5 (also known as TASK-2 and K(2P)5.1) in activated T cell physiology has only recently been described. So far KCNK5 has been described to be up-regulated in T cells in multiple sclerosis patients and to be implicated in the volume regulatory mechanism regulatory volume decrease (RVD) in T cells.<br />Methods: We investigated the time-dependent expression pattern of KCNK5 in CD3/CD28 activated human T cells using qPCR and Western blotting and its role in RVD using a Coulter Counter.<br />Results: KCNK5 is highly up-regulated in CD3/CD28 activated T cells both at mRNA (after 24 h) and protein level (72 and 144 h), but despite this up-regulation the RVD response is inhibited. Furthermore, the swelling-activated Cl- permeability in activated T cells is strongly decreased, and the RVD inhibition is predominantly due to the decreased Cl- permeability.<br />Conclusion: The up-regulated KCNK5 in activated human T cells does not play a volume regulatory role, due to decreased Cl- permeability. We speculate that the KCNK5 up-regulation might play a role in hyperpolarization of the cell membrane leading to increased Ca2+ influx and proliferation of T cells.<br /> (© 2016 S. Karger AG, Basel.)
- Subjects :
- CD28 Antigens metabolism
CD3 Complex pharmacology
Calcium metabolism
Cell Size drug effects
Chlorine metabolism
Humans
Intermediate-Conductance Calcium-Activated Potassium Channels genetics
Lymphocyte Activation
Potassium Channels, Tandem Pore Domain genetics
Potassium Channels, Tandem Pore Domain metabolism
T-Lymphocytes metabolism
Up-Regulation
Subjects
Details
- Language :
- English
- ISSN :
- 1421-9778
- Volume :
- 38
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 26909737
- Full Text :
- https://doi.org/10.1159/000443042