TRPM4 channels in the cardiovascular system: physiology, pathophysiology, and pharmacology.

The transient receptor potential channel (TRP) family comprises at least 28 genes in the human genome. These channels are widely expressed in many different tissues, including those of the cardiovascular system. The transient receptor potential channel melastatin 4 (TRPM4) is a Ca(2+)-activated non-specific cationic channel, which is impermeable to Ca(2+). TRPM4 is expressed in many cells of the cardiovascular system, such as cardiac cells of the conduction pathway and arterial and venous smooth muscle cells. This review article summarizes the recently described roles of TRPM4 in normal physiology and in various disease states. Genetic variants in the human gene TRPM4 have been linked to several cardiac conduction disorders. TRPM4 has also been proposed to play a crucial role in secondary hemorrhage following spinal cord injuries. Spontaneously hypertensive rats with cardiac hypertrophy were shown to over-express the cardiac TRPM4 channel. Recent studies suggest that TRPM4 plays an important role in cardiovascular physiology and disease, even if most of the molecular and cellular mechanisms have yet to be elucidated. We conclude this review article with a brief overview of the compounds that have been shown to either inhibit or activate TRPM4 under experimental conditions. Based on recent findings, the TRPM4 channel can be proposed as a future target for the pharmacological treatment of cardiovascular disorders, such as hypertension and cardiac arrhythmias.

[1]  N. Stockbridge Etiology of the supernormal period. , 1988, Biophysical journal.

[2]  R. Tsien,et al.  Ionic basis of transient inward current induced by strophanthidin in cardiac Purkinje fibres. , 1978, The Journal of physiology.

[3]  P. Launay,et al.  TRPM4, a Ca2+-activated nonselective cation channel in mouse sino-atrial node cells. , 2007, Cardiovascular research.

[4]  R Weingart,et al.  Role of calcium ions in transient inward currents and aftercontractions induced by strophanthidin in cardiac Purkinje fibres. , 1978, The Journal of physiology.

[5]  J. Kinet,et al.  The calcium-activated nonselective cation channel TRPM4 is essential for the migration but not the maturation of dendritic cells , 2008, Nature Immunology.

[6]  M. Zhu,et al.  The Selectivity Filter of the Cation Channel TRPM4* , 2005, Journal of Biological Chemistry.

[7]  J. Simard,et al.  De novo expression of Trpm4 initiates secondary hemorrhage in spinal cord injury , 2009, Nature Medicine.

[8]  D. Oh,et al.  Calcium oscillations regulate thymocyte motility during positive selection in the three-dimensional thymic environment , 2005, Nature Immunology.

[9]  P. Bois,et al.  Calcium-activated nonselective cation channels in mammalian cardiomyocytes. , 2006, Trends in cardiovascular medicine.

[10]  Y. Rudy,et al.  Basic mechanisms of cardiac impulse propagation and associated arrhythmias. , 2004, Physiological reviews.

[11]  M. Freichel,et al.  Increased catecholamine secretion contributes to hypertension in TRPM4-deficient mice. , 2010, The Journal of clinical investigation.

[12]  M. Cahalan,et al.  Mitogen-induced oscillations of cytosolic Ca2+ and transmembrane Ca2+ current in human leukemic T cells. , 1989, Cell regulation.

[13]  J. Kinet,et al.  TRPM4 Regulates Calcium Oscillations After T Cell Activation , 2004, Science.

[14]  O. Pongs,et al.  Gain-of-Function Mutations in TRPM4 Cause Autosomal Dominant Isolated Cardiac Conduction Disease , 2010, Circulation. Cardiovascular genetics.

[15]  E. Neher,et al.  Inward current channels activated by intracellular Ca in cultured cardiac cells , 1981, Nature.

[16]  R. Dolmetsch,et al.  Signaling between intracellular Ca2+ stores and depletion-activated Ca2+ channels generates [Ca2+]i oscillations in T lymphocytes , 1994, The Journal of general physiology.

[17]  K. Sipido,et al.  Inhibition of the calcium-activated chloride current in cardiac ventricular myocytes by N-(p-amylcinnamoyl)anthranilic acid (ACA). , 2010, Biochemical and biophysical research communications.

[18]  Bernd Nilius,et al.  Heat activation of TRPM5 underlies thermal sensitivity of sweet taste , 2005, Nature.

[19]  M. Tamkun,et al.  Vasoconstriction resulting from dynamic membrane trafficking of TRPM4 in vascular smooth muscle cells. , 2010, American journal of physiology. Cell physiology.

[20]  S. Earley,et al.  Pharmacological inhibition of TRPM4 hyperpolarizes vascular smooth muscle. , 2010, American journal of physiology. Cell physiology.

[21]  D. Clapham,et al.  An introduction to TRP channels. , 2006, Annual review of physiology.

[22]  H. Brinkmeier,et al.  Tissue-specific expression of TRP channel genes in the mouse and its variation in three different mouse strains , 2006, BMC Genomics.

[23]  R. Rouet,et al.  Transient receptor potential melastatin 4 inhibitor 9‐phenanthrol abolishes arrhythmias induced by hypoxia and re‐oxygenation in mouse ventricle , 2012, British journal of pharmacology.

[24]  S L Mironov,et al.  Metabotropic glutamate receptors activate dendritic calcium waves and TRPM channels which drive rhythmic respiratory patterns in mice , 2008, The Journal of physiology.

[25]  P. Tran Ba Huy,et al.  A calcium-activated nonselective cationic channel in the basolateral membrane of outer hair cells of the guinea-pig cochlea , 1994, Pflügers Archiv.

[26]  R. Vennekens,et al.  From cardiac cation channels to the molecular dissection of the transient receptor potential channel TRPM4 , 2006, Pflügers Archiv.

[27]  K. Sanders,et al.  Basally activated nonselective cation currents regulate the resting membrane potential in human and monkey colonic smooth muscle. , 2011, American journal of physiology. Gastrointestinal and liver physiology.

[28]  R. Vennekens,et al.  Comparison of functional properties of the Ca2+-activated cation channels TRPM4 and TRPM5 from mice. , 2005, Cell calcium.

[29]  U. Panten,et al.  Structural requirements of sulphonylureas and analogues for interaction with sulphonylurea receptor subtypes , 1999, British journal of pharmacology.

[30]  B. Nilius,et al.  Decavanadate modulates gating of TRPM4 cation channels , 2004, The Journal of physiology.

[31]  R. Vaughan-Jones,et al.  Do calcium-activated potassium channels exist in the heart? , 1983, Cell calcium.

[32]  B. Nilius,et al.  Intracellular nucleotides and polyamines inhibit the Ca2+-activated cation channel TRPM4b , 2004, Pflügers Archiv.

[33]  S. Earley,et al.  Ca2+ release from the sarcoplasmic reticulum is required for sustained TRPM4 activity in cerebral artery smooth muscle cells. , 2010, American journal of physiology. Cell physiology.

[34]  Craig Montell,et al.  International Union of Pharmacology. XLIX. Nomenclature and Structure-Function Relationships of Transient Receptor Potential Channels , 2005, Pharmacological Reviews.

[35]  H. Brinkmeier,et al.  Transient receptor potential cation channels in normal and dystrophic mdx muscle , 2008, Neuromuscular Disorders.

[36]  W. Lederer,et al.  The arrhythmogenic current ITI in the absence of electrogenic sodium‐calcium exchange in sheep cardiac Purkinje fibres. , 1986, The Journal of physiology.

[37]  M. Hoth,et al.  Potent Inhibition of Ca2+ Release-activated Ca2+ Channels and T-lymphocyte Activation by the Pyrazole Derivative BTP2* , 2004, Journal of Biological Chemistry.

[38]  C. Nichols,et al.  On Potential Interactions between Non-selective Cation Channel TRPM4 and Sulfonylurea Receptor SUR1* , 2012, The Journal of Biological Chemistry.

[39]  P. Launay,et al.  Physiological roles of the TRPM4 channel extracted from background currents. , 2010, Physiology.

[40]  J. Simard,et al.  Molecular mechanisms of microvascular failure in central nervous system injury--synergistic roles of NKCC1 and SUR1/TRPM4. , 2010, Journal of neurosurgery.

[41]  P. Bois,et al.  Functional characterization of a Ca2+‐activated non‐selective cation channel in human atrial cardiomyocytes , 2004, The Journal of physiology.

[42]  M. Nelson,et al.  Membrane stretch-induced activation of a TRPM4-like nonselective cation channel in cerebral artery myocytes. , 2007, Journal of pharmacological sciences.

[43]  E. Schulze-Bahr,et al.  Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I. , 2009, Journal of Clinical Investigation.

[44]  J. Kinet,et al.  A Pyrazole Derivative Potently Inhibits Lymphocyte Ca2+ Influx and Cytokine Production by Facilitating Transient Receptor Potential Melastatin 4 Channel Activity , 2006, Molecular Pharmacology.

[45]  B F Hoffman,et al.  Cellular mechanisms for cardiac arrhythmias. , 1981, Circulation research.

[46]  R. Guinamard Determination of channel properties at the unitary level in adult mammalian isolated cardiomyocytes. , 2007, Methods in molecular biology.

[47]  J. Soboloff,et al.  A Functional Link between Store-operated and TRPC Channels Revealed by the 3,5-Bis(trifluoromethyl)pyrazole Derivative, BTP2* , 2005, Journal of Biological Chemistry.

[48]  W. Kuebler,et al.  Mechanotransduction by TRP Channels: General Concepts and Specific Role in the Vasculature , 2009, Cell Biochemistry and Biophysics.

[49]  Takahiro Shimizu,et al.  TRPM4 regulates migration of mast cells in mice. , 2009, Cell calcium.

[50]  M. Zhu,et al.  Regulation of the Ca2+ Sensitivity of the Nonselective Cation Channel TRPM4* , 2005, Journal of Biological Chemistry.

[51]  M. Murakami,et al.  Identification and characterization of the murine TRPM4 channel. , 2003, Biochemical and biophysical research communications.

[52]  C. Montell,et al.  Regulation of melastatin, a TRP-related protein, through interaction with a cytoplasmic isoform , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[53]  Allan R. Jones,et al.  Genome-wide atlas of gene expression in the adult mouse brain , 2007, Nature.

[54]  J. Hill,et al.  Reconstitution and characterization of a calcium-activated channel from heart. , 1988, Circulation research.

[55]  Alexander J Stokes,et al.  TRPM4 controls insulin secretion in pancreatic β-cells , 2007 .

[56]  S. Earley,et al.  Critical Role for Transient Receptor Potential Channel TRPM4 in Myogenic Constriction of Cerebral Arteries , 2004, Circulation research.

[57]  R. Brugada,et al.  Phenotypical Manifestations of Mutations in the Genes Encoding Subunits of the Cardiac Voltage – Dependent L-Type Calcium Channel , 2011 .

[58]  Eric Schulze-Bahr,et al.  Mutational spectrum in the Ca2+‐activated cation channel gene TRPM4 in patients with cardiac conductance disturbances , 2012, Human mutation.

[59]  D. Beech EMERGING FUNCTIONS OF 10 TYPES OF TRP CATIONIC CHANNEL IN VASCULAR SMOOTH MUSCLE , 2005, Clinical and experimental pharmacology & physiology.

[60]  V. Ádám-Vizi,et al.  Ca(2+)- and voltage-dependent gating of Ca(2+)- and ATP-sensitive cationic channels in brain capillary endothelium. , 2003, Biophysical journal.

[61]  H. Fozzard,et al.  Influence of Extracellular K+ Concentration on Cable Properties and Excitability of Sheep Cardiac Purkinje Fibers , 1970, Circulation research.

[62]  P. Murdock,et al.  Tissue Distribution Profiles of the Human TRPM Cation Channel Family , 2006, Journal of receptor and signal transduction research.

[63]  P. Launay,et al.  9‐Phenanthrol inhibits human TRPM4 but not TRPM5 cationic channels , 2008, British journal of pharmacology.

[64]  P. Bois,et al.  Functional Expression of the TRPM4 Cationic Current in Ventricular Cardiomyocytes From Spontaneously Hypertensive Rats , 2006, Hypertension.

[65]  J. Spear,et al.  Supernormal Excitability and Conduction in the His‐Purkinje System of the Dog , 1974, Circulation research.

[66]  V. Joulin,et al.  The SK3/KCa2.3 potassium channel is a new cellular target for edelfosine , 2011, British journal of pharmacology.