Signature channels of excitability no more: L-type channels in immune cells

Although the concept of Ca2+ as a uni¬versal messenger is well established, it was assumed that the regulatory mechanisms of Ca2+-signal¬ing were divided along the line of electric excitability. Recent advances in molecular biology and genomics have however provided evidence that non-excitable cells...

Full description

Bibliographic Details
Main Authors: Bennett eDavenport, Yuan eLi, Justin W. Heizer, Carsten eSchmitz, Anne-Laure ePerraud
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-07-01
Series:Frontiers in Immunology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fimmu.2015.00375/full
_version_ 1818535087053996032
author Bennett eDavenport
Yuan eLi
Justin W. Heizer
Carsten eSchmitz
Anne-Laure ePerraud
author_facet Bennett eDavenport
Yuan eLi
Justin W. Heizer
Carsten eSchmitz
Anne-Laure ePerraud
author_sort Bennett eDavenport
collection DOAJ
description Although the concept of Ca2+ as a uni¬versal messenger is well established, it was assumed that the regulatory mechanisms of Ca2+-signal¬ing were divided along the line of electric excitability. Recent advances in molecular biology and genomics have however provided evidence that non-excitable cells such as immunocytes also express a wide and diverse pool of ion channels that does not differ as significantly from that of excitable cells as originally assumed. Ion channels and transporters are involved in virtually all aspects of immune response regulation, from cell differentiation and development, to activation, and effector functions such as migration, antibody-secretion, phagosomal maturation, or vesicular delivery of bactericidal agents. This comprises TRP channel family members, voltage- and Ca2+-gated K+- and Na+-channels, as well as unexpectedly, components of the CaV1-subfamily of voltage-gated L-type Ca2+-channels, originally thought to be signature molecules of excitability. This article provides an overview of recent observations made in the field of CaV1 L-type channel function in the immune context, as well as presents results we obtained studying these channels in B-lymphocytes.
first_indexed 2024-12-11T18:20:09Z
format Article
id doaj.art-cc7db4e3a223432ea3723eb9bb463527
institution Directory Open Access Journal
issn 1664-3224
language English
last_indexed 2024-12-11T18:20:09Z
publishDate 2015-07-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Immunology
spelling doaj.art-cc7db4e3a223432ea3723eb9bb4635272022-12-22T00:55:17ZengFrontiers Media S.A.Frontiers in Immunology1664-32242015-07-01610.3389/fimmu.2015.00375145077Signature channels of excitability no more: L-type channels in immune cellsBennett eDavenport0Yuan eLi1Justin W. Heizer2Carsten eSchmitz3Anne-Laure ePerraud4National Jewish Health, University of Colorado DenverNational Jewish Health, University of Colorado DenverNational Jewish Health, University of Colorado DenverNational Jewish Health, University of Colorado DenverNational Jewish Health, University of Colorado DenverAlthough the concept of Ca2+ as a uni¬versal messenger is well established, it was assumed that the regulatory mechanisms of Ca2+-signal¬ing were divided along the line of electric excitability. Recent advances in molecular biology and genomics have however provided evidence that non-excitable cells such as immunocytes also express a wide and diverse pool of ion channels that does not differ as significantly from that of excitable cells as originally assumed. Ion channels and transporters are involved in virtually all aspects of immune response regulation, from cell differentiation and development, to activation, and effector functions such as migration, antibody-secretion, phagosomal maturation, or vesicular delivery of bactericidal agents. This comprises TRP channel family members, voltage- and Ca2+-gated K+- and Na+-channels, as well as unexpectedly, components of the CaV1-subfamily of voltage-gated L-type Ca2+-channels, originally thought to be signature molecules of excitability. This article provides an overview of recent observations made in the field of CaV1 L-type channel function in the immune context, as well as presents results we obtained studying these channels in B-lymphocytes.http://journal.frontiersin.org/Journal/10.3389/fimmu.2015.00375/fullCalcium SignalingDihydropyridinesLymphocytesMyeloid lineageL-type channelsCaV ion channels
spellingShingle Bennett eDavenport
Yuan eLi
Justin W. Heizer
Carsten eSchmitz
Anne-Laure ePerraud
Signature channels of excitability no more: L-type channels in immune cells
Frontiers in Immunology
Calcium Signaling
Dihydropyridines
Lymphocytes
Myeloid lineage
L-type channels
CaV ion channels
title Signature channels of excitability no more: L-type channels in immune cells
title_full Signature channels of excitability no more: L-type channels in immune cells
title_fullStr Signature channels of excitability no more: L-type channels in immune cells
title_full_unstemmed Signature channels of excitability no more: L-type channels in immune cells
title_short Signature channels of excitability no more: L-type channels in immune cells
title_sort signature channels of excitability no more l type channels in immune cells
topic Calcium Signaling
Dihydropyridines
Lymphocytes
Myeloid lineage
L-type channels
CaV ion channels
url http://journal.frontiersin.org/Journal/10.3389/fimmu.2015.00375/full
work_keys_str_mv AT bennettedavenport signaturechannelsofexcitabilitynomoreltypechannelsinimmunecells
AT yuaneli signaturechannelsofexcitabilitynomoreltypechannelsinimmunecells
AT justinwheizer signaturechannelsofexcitabilitynomoreltypechannelsinimmunecells
AT carsteneschmitz signaturechannelsofexcitabilitynomoreltypechannelsinimmunecells
AT annelaureeperraud signaturechannelsofexcitabilitynomoreltypechannelsinimmunecells