Ion channels in T lymphocytes: an update on facts, mechanisms and therapeutic targeting in autoimmune diseases
- PMID: 20026117
- DOI: 10.1016/j.imlet.2009.12.015
Ion channels in T lymphocytes: an update on facts, mechanisms and therapeutic targeting in autoimmune diseases
Abstract
During the last quarter of a century a large body of evidence was gathered about the involvement of ion channels in T lymphocyte activation. A series of remarkable findings promoted T cell ion channels to become potential pharmaceutical targets in the therapy of autoimmune disorders. Numerous comprehensive reviews describe the types of ion channels found in the plasma membrane of T cells and their roles in signaling pathways leading to activation, the changes in the expression of these channels brought upon by differentiation to various T cell subsets, the formation and possible functions of signaling molecular clusters that include ion channels in the immunological synapse, the discovery and refinement of structurally different ion channel blockers and the successful in vivo application of such compounds to suppress hypersensitivity reactions and autoimmune processes. In this review we wish to provide a concise update on these topics from recent years, highlighting the most notable developments.
Copyright 2009 Elsevier B.V. All rights reserved.
Similar articles
-
Ion channels in T cells: from molecular pharmacology to therapy.Arch Immunol Ther Exp (Warsz). 2005 Mar-Apr;53(2):127-35. Arch Immunol Ther Exp (Warsz). 2005. PMID: 15928581 Review.
-
Potassium channels as therapeutic targets for autoimmune disorders.Curr Opin Drug Discov Devel. 2003 Sep;6(5):640-7. Curr Opin Drug Discov Devel. 2003. PMID: 14579513 Review.
-
Functional consequences of Kv1.3 ion channel rearrangement into the immunological synapse.Immunol Lett. 2009 Jun 30;125(1):15-21. doi: 10.1016/j.imlet.2009.05.004. Epub 2009 May 27. Immunol Lett. 2009. PMID: 19477198
-
Toxins Targeting the Kv1.3 Channel: Potential Immunomodulators for Autoimmune Diseases.Toxins (Basel). 2015 May 19;7(5):1749-64. doi: 10.3390/toxins7051749. Toxins (Basel). 2015. PMID: 25996605 Free PMC article. Review.
-
Ion channels and lymphocyte activation.Immunol Lett. 2004 Mar 29;92(1-2):55-66. doi: 10.1016/j.imlet.2003.11.020. Immunol Lett. 2004. PMID: 15081528 Review.
Cited by
-
The C-terminal domain of Kv1.3 regulates functional interactions with the KCNE4 subunit.J Cell Sci. 2016 Nov 15;129(22):4265-4277. doi: 10.1242/jcs.191650. Epub 2016 Oct 6. J Cell Sci. 2016. PMID: 27802162 Free PMC article.
-
A New Concept of Biotensegrity Incorporating Liquid Tissues: Blood and Lymph.J Evid Based Integr Med. 2018 Jan-Dec;23:2515690X18792838. doi: 10.1177/2515690X18792838. J Evid Based Integr Med. 2018. PMID: 30124054 Free PMC article.
-
Application of a modified multifunctional short peptide in the treatment of periodontitis.Sci Rep. 2024 Oct 1;14(1):22855. doi: 10.1038/s41598-024-69933-z. Sci Rep. 2024. PMID: 39353971 Free PMC article.
-
Meaning of the Solid and Liquid Fascia to Reconsider the Model of Biotensegrity.Cureus. 2018 Jul 5;10(7):e2922. doi: 10.7759/cureus.2922. Cureus. 2018. PMID: 30197845 Free PMC article. Review.
-
Differentially Expressed Potassium Channels Are Associated with Function of Human Effector Memory CD8+ T Cells.Front Immunol. 2017 Jul 24;8:859. doi: 10.3389/fimmu.2017.00859. eCollection 2017. Front Immunol. 2017. PMID: 28791017 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical