The secret life of ion channels: Kv1.3 potassium channels and proliferation
Kv1.3 channels are involved in the switch to proliferation of normally quiescent cells, being implicated in the control of cell cycle in many different cell types and in many different ways. They modulate membrane potential controlling K fluxes, sense changes in potential, and interact with many sig...
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Veröffentlicht in: | American Journal of Physiology: Cell Physiology 2018-01, Vol.314 (1), p.C27-C42 |
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description | Kv1.3 channels are involved in the switch to proliferation of normally quiescent cells, being implicated in the control of cell cycle in many different cell types and in many different ways. They modulate membrane potential controlling K
fluxes, sense changes in potential, and interact with many signaling molecules through their intracellular domains. From a mechanistic point of view, we can describe the role of Kv1.3 channels in proliferation with at least three different models. In the "membrane potential model," membrane hyperpolarization resulting from Kv1.3 activation provides the driving force for Ca
influx required to activate Ca
-dependent transcription. This model explains most of the data obtained from several cells from the immune system. In the "voltage sensor model," Kv1.3 channels serve mainly as sensors that transduce electrical signals into biochemical cascades, independently of their effect on membrane potential. Kv1.3-dependent proliferation of vascular smooth muscle cells (VSMCs) could fit this model. Finally, in the "channelosome balance model," the master switch determining proliferation may be related to the control of the Kv1.3 to Kv1.5 ratio, as described in glial cells and also in VSMCs. Since the three mechanisms cannot function independently, these models are obviously not exclusive. Nevertheless, they could be exploited differentially in different cells and tissues. This large functional flexibility of Kv1.3 channels surely gives a new perspective on their functions beyond their elementary role as ion channels, although a conclusive picture of the mechanisms involved in Kv1.3 signaling to proliferation is yet to be reached. |
doi_str_mv | 10.1152/ajpcell.00136.2017 |
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fluxes, sense changes in potential, and interact with many signaling molecules through their intracellular domains. From a mechanistic point of view, we can describe the role of Kv1.3 channels in proliferation with at least three different models. In the "membrane potential model," membrane hyperpolarization resulting from Kv1.3 activation provides the driving force for Ca
influx required to activate Ca
-dependent transcription. This model explains most of the data obtained from several cells from the immune system. In the "voltage sensor model," Kv1.3 channels serve mainly as sensors that transduce electrical signals into biochemical cascades, independently of their effect on membrane potential. Kv1.3-dependent proliferation of vascular smooth muscle cells (VSMCs) could fit this model. Finally, in the "channelosome balance model," the master switch determining proliferation may be related to the control of the Kv1.3 to Kv1.5 ratio, as described in glial cells and also in VSMCs. Since the three mechanisms cannot function independently, these models are obviously not exclusive. Nevertheless, they could be exploited differentially in different cells and tissues. This large functional flexibility of Kv1.3 channels surely gives a new perspective on their functions beyond their elementary role as ion channels, although a conclusive picture of the mechanisms involved in Kv1.3 signaling to proliferation is yet to be reached.</description><identifier>ISSN: 0363-6143</identifier><identifier>EISSN: 1522-1563</identifier><identifier>DOI: 10.1152/ajpcell.00136.2017</identifier><identifier>PMID: 28931540</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Calcium influx ; Calcium Signaling ; Cell cycle ; Cell proliferation ; Cell Proliferation - drug effects ; Cells ; Glial cells ; Humans ; Hyperpolarization ; Immune system ; Intracellular signalling ; Ion Channel Gating ; Kv1.3 Potassium Channel - antagonists & inhibitors ; Kv1.3 Potassium Channel - chemistry ; Kv1.3 Potassium Channel - genetics ; Kv1.3 Potassium Channel - metabolism ; Membrane potential ; Membrane Potentials ; Membranes ; Models, Biological ; Molecules ; Potassium - metabolism ; Potassium Channel Blockers - pharmacology ; Potassium channels (voltage-gated) ; Protein Conformation ; Proteins ; Smooth muscle ; Structure-Activity Relationship ; Transcription ; Transcription factors</subject><ispartof>American Journal of Physiology: Cell Physiology, 2018-01, Vol.314 (1), p.C27-C42</ispartof><rights>Copyright American Physiological Society Jan 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c397t-6088b49d11f90f121e46e70bdf0422913116712897aab560fe82a0025f2e0d6a3</citedby><cites>FETCH-LOGICAL-c397t-6088b49d11f90f121e46e70bdf0422913116712897aab560fe82a0025f2e0d6a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3026,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28931540$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pérez-García, M Teresa</creatorcontrib><creatorcontrib>Cidad, Pilar</creatorcontrib><creatorcontrib>López-López, José R</creatorcontrib><title>The secret life of ion channels: Kv1.3 potassium channels and proliferation</title><title>American Journal of Physiology: Cell Physiology</title><addtitle>Am J Physiol Cell Physiol</addtitle><description>Kv1.3 channels are involved in the switch to proliferation of normally quiescent cells, being implicated in the control of cell cycle in many different cell types and in many different ways. They modulate membrane potential controlling K
fluxes, sense changes in potential, and interact with many signaling molecules through their intracellular domains. From a mechanistic point of view, we can describe the role of Kv1.3 channels in proliferation with at least three different models. In the "membrane potential model," membrane hyperpolarization resulting from Kv1.3 activation provides the driving force for Ca
influx required to activate Ca
-dependent transcription. This model explains most of the data obtained from several cells from the immune system. In the "voltage sensor model," Kv1.3 channels serve mainly as sensors that transduce electrical signals into biochemical cascades, independently of their effect on membrane potential. Kv1.3-dependent proliferation of vascular smooth muscle cells (VSMCs) could fit this model. Finally, in the "channelosome balance model," the master switch determining proliferation may be related to the control of the Kv1.3 to Kv1.5 ratio, as described in glial cells and also in VSMCs. Since the three mechanisms cannot function independently, these models are obviously not exclusive. Nevertheless, they could be exploited differentially in different cells and tissues. This large functional flexibility of Kv1.3 channels surely gives a new perspective on their functions beyond their elementary role as ion channels, although a conclusive picture of the mechanisms involved in Kv1.3 signaling to proliferation is yet to be reached.</description><subject>Animals</subject><subject>Calcium influx</subject><subject>Calcium Signaling</subject><subject>Cell cycle</subject><subject>Cell proliferation</subject><subject>Cell Proliferation - drug effects</subject><subject>Cells</subject><subject>Glial cells</subject><subject>Humans</subject><subject>Hyperpolarization</subject><subject>Immune system</subject><subject>Intracellular signalling</subject><subject>Ion Channel Gating</subject><subject>Kv1.3 Potassium Channel - antagonists & inhibitors</subject><subject>Kv1.3 Potassium Channel - chemistry</subject><subject>Kv1.3 Potassium Channel - genetics</subject><subject>Kv1.3 Potassium Channel - metabolism</subject><subject>Membrane potential</subject><subject>Membrane Potentials</subject><subject>Membranes</subject><subject>Models, Biological</subject><subject>Molecules</subject><subject>Potassium - metabolism</subject><subject>Potassium Channel Blockers - pharmacology</subject><subject>Potassium channels (voltage-gated)</subject><subject>Protein Conformation</subject><subject>Proteins</subject><subject>Smooth muscle</subject><subject>Structure-Activity Relationship</subject><subject>Transcription</subject><subject>Transcription factors</subject><issn>0363-6143</issn><issn>1522-1563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkD1PwzAQhi0EoqXwBxiQJRaWhDs7cWI2VPGlVmIpc-QktpoqX9gJEv8eh5YOTDfc8969egi5RggRY3avdn2h6zoEQC5CBpickLlfsABjwU_JHLjggcCIz8iFczsAiJiQ52TGUskxjmBOVputpk4XVg-0roymnaFV19Jiq9pW1-6Brr4w5LTvBuVcNTbHDVVtSXvbTSmrBh-6JGdG1U5fHeaCfDw_bZavwfr95W35uA4KLpMhEJCmeSRLRCPBIEMdCZ1AXhpfj0nkiCJBXzFRKo8FGJ0yBcBiwzSUQvEFudvf9d8_R-2GrKncZEK1uhtdhjLyQuJEoEdv_6G7brStb-epNOGxZFHiKbanCts5Z7XJels1yn5nCNmkOjuozn5VZ5NqH7o5nB7zRpfHyJ9b_gPTXXjb</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Pérez-García, M Teresa</creator><creator>Cidad, Pilar</creator><creator>López-López, José R</creator><general>American Physiological Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TS</scope><scope>7X8</scope></search><sort><creationdate>20180101</creationdate><title>The secret life of ion channels: Kv1.3 potassium channels and proliferation</title><author>Pérez-García, M Teresa ; Cidad, Pilar ; López-López, José R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c397t-6088b49d11f90f121e46e70bdf0422913116712897aab560fe82a0025f2e0d6a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Calcium influx</topic><topic>Calcium Signaling</topic><topic>Cell cycle</topic><topic>Cell proliferation</topic><topic>Cell Proliferation - drug effects</topic><topic>Cells</topic><topic>Glial cells</topic><topic>Humans</topic><topic>Hyperpolarization</topic><topic>Immune system</topic><topic>Intracellular signalling</topic><topic>Ion Channel Gating</topic><topic>Kv1.3 Potassium Channel - antagonists & inhibitors</topic><topic>Kv1.3 Potassium Channel - chemistry</topic><topic>Kv1.3 Potassium Channel - genetics</topic><topic>Kv1.3 Potassium Channel - metabolism</topic><topic>Membrane potential</topic><topic>Membrane Potentials</topic><topic>Membranes</topic><topic>Models, Biological</topic><topic>Molecules</topic><topic>Potassium - metabolism</topic><topic>Potassium Channel Blockers - pharmacology</topic><topic>Potassium channels (voltage-gated)</topic><topic>Protein Conformation</topic><topic>Proteins</topic><topic>Smooth muscle</topic><topic>Structure-Activity Relationship</topic><topic>Transcription</topic><topic>Transcription factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pérez-García, M Teresa</creatorcontrib><creatorcontrib>Cidad, Pilar</creatorcontrib><creatorcontrib>López-López, José R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Physical Education Index</collection><collection>MEDLINE - Academic</collection><jtitle>American Journal of Physiology: Cell Physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pérez-García, M Teresa</au><au>Cidad, Pilar</au><au>López-López, José R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The secret life of ion channels: Kv1.3 potassium channels and proliferation</atitle><jtitle>American Journal of Physiology: Cell Physiology</jtitle><addtitle>Am J Physiol Cell Physiol</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>314</volume><issue>1</issue><spage>C27</spage><epage>C42</epage><pages>C27-C42</pages><issn>0363-6143</issn><eissn>1522-1563</eissn><abstract>Kv1.3 channels are involved in the switch to proliferation of normally quiescent cells, being implicated in the control of cell cycle in many different cell types and in many different ways. They modulate membrane potential controlling K
fluxes, sense changes in potential, and interact with many signaling molecules through their intracellular domains. From a mechanistic point of view, we can describe the role of Kv1.3 channels in proliferation with at least three different models. In the "membrane potential model," membrane hyperpolarization resulting from Kv1.3 activation provides the driving force for Ca
influx required to activate Ca
-dependent transcription. This model explains most of the data obtained from several cells from the immune system. In the "voltage sensor model," Kv1.3 channels serve mainly as sensors that transduce electrical signals into biochemical cascades, independently of their effect on membrane potential. Kv1.3-dependent proliferation of vascular smooth muscle cells (VSMCs) could fit this model. Finally, in the "channelosome balance model," the master switch determining proliferation may be related to the control of the Kv1.3 to Kv1.5 ratio, as described in glial cells and also in VSMCs. Since the three mechanisms cannot function independently, these models are obviously not exclusive. Nevertheless, they could be exploited differentially in different cells and tissues. This large functional flexibility of Kv1.3 channels surely gives a new perspective on their functions beyond their elementary role as ion channels, although a conclusive picture of the mechanisms involved in Kv1.3 signaling to proliferation is yet to be reached.</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>28931540</pmid><doi>10.1152/ajpcell.00136.2017</doi></addata></record> |
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subjects | Animals Calcium influx Calcium Signaling Cell cycle Cell proliferation Cell Proliferation - drug effects Cells Glial cells Humans Hyperpolarization Immune system Intracellular signalling Ion Channel Gating Kv1.3 Potassium Channel - antagonists & inhibitors Kv1.3 Potassium Channel - chemistry Kv1.3 Potassium Channel - genetics Kv1.3 Potassium Channel - metabolism Membrane potential Membrane Potentials Membranes Models, Biological Molecules Potassium - metabolism Potassium Channel Blockers - pharmacology Potassium channels (voltage-gated) Protein Conformation Proteins Smooth muscle Structure-Activity Relationship Transcription Transcription factors |
title | The secret life of ion channels: Kv1.3 potassium channels and proliferation |
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