Literature DB >> 12799367

Voltage dependence of the Ca2+-activated cation channel TRPM4.

Bernd Nilius1, Jean Prenen, Guy Droogmans, Thomas Voets, Rudi Vennekens, Marc Freichel, Ulrich Wissenbach, Veit Flockerzi.   

Abstract

TRPM4 is a Ca2+-activated but Ca2+-impermeable cation channel. An increase of [Ca2+]i induces activation and subsequent reduction of currents through TRPM4 channels. This inactivation is strikingly decreased in cell-free patches. In whole cell and cell-free configuration, currents through TRPM4 deactivate rapidly at negative potentials. At positive potentials, currents are much larger and activate slowly. This voltage-dependent behavior induces a striking outward rectification of the steady state currents. The instantaneous current-voltage relationship, derived from the amplitude of tail currents following a prepulse to positive potentials, is linear. Currents show a Boltzmann type of activation; the fraction of open channels increases at positive potentials and is low at negative potentials. Voltage dependence is not due to block by divalent cations or to voltage-dependent binding of intracellular Ca2+ to an activator site, indicating that TRPM4 is a transient receptor potential channel with an intrinsic voltage-sensing mechanism. Voltage dependence of TRPM4 may be functionally important, especially in excitable tissues generating plateau-like or bursting action potentials.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12799367     DOI: 10.1074/jbc.M305127200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  132 in total

Review 1.  Vanilloid and melastatin transient receptor potential channels in vascular smooth muscle.

Authors:  Scott Earley
Journal:  Microcirculation       Date:  2010-05       Impact factor: 2.628

2.  TRPM5 is a transient Ca2+-activated cation channel responding to rapid changes in [Ca2+]i.

Authors:  Dirk Prawitt; Mahealani K Monteilh-Zoller; Lili Brixel; Christian Spangenberg; Bernhard Zabel; Andrea Fleig; Reinhold Penner
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-21       Impact factor: 11.205

Review 3.  International Union of Basic and Clinical Pharmacology. LXXVI. Current progress in the mammalian TRP ion channel family.

Authors:  Long-Jun Wu; Tara-Beth Sweet; David E Clapham
Journal:  Pharmacol Rev       Date:  2010-09       Impact factor: 25.468

Review 4.  Pharmacology of transient receptor potential melastatin channels in the vasculature.

Authors:  Alexander Zholos
Journal:  Br J Pharmacol       Date:  2010-03-05       Impact factor: 8.739

Review 5.  Emerging concepts for the role of TRP channels in the cardiovascular system.

Authors:  Rudi Vennekens
Journal:  J Physiol       Date:  2010-12-20       Impact factor: 5.182

6.  Rho kinase activity governs arteriolar myogenic depolarization.

Authors:  Yao Li; Joseph E Brayden
Journal:  J Cereb Blood Flow Metab       Date:  2015-12-07       Impact factor: 6.200

7.  Structure of the human TRPM4 ion channel in a lipid nanodisc.

Authors:  Henriette E Autzen; Alexander G Myasnikov; Melody G Campbell; Daniel Asarnow; David Julius; Yifan Cheng
Journal:  Science       Date:  2017-12-07       Impact factor: 47.728

8.  TRPM4 inhibition promotes angiogenesis after ischemic stroke.

Authors:  Kok Poh Loh; Gandi Ng; Chye Yun Yu; Chee Kong Fhu; Dejie Yu; Rudi Vennekens; Bernd Nilius; Tuck Wah Soong; Ping Liao
Journal:  Pflugers Arch       Date:  2013-09-17       Impact factor: 3.657

9.  Regulation of the murine TRPP3 channel by voltage, pH, and changes in cell volume.

Authors:  Takahiro Shimizu; Annelies Janssens; Thomas Voets; Bernd Nilius
Journal:  Pflugers Arch       Date:  2008-07-29       Impact factor: 3.657

10.  Decavanadate modulates gating of TRPM4 cation channels.

Authors:  Bernd Nilius; Jean Prenen; Annelies Janssens; Thomas Voets; Guy Droogmans
Journal:  J Physiol       Date:  2004-08-26       Impact factor: 5.182

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.