DYNAMIC OF ION CHANNEL EXPRESSION AT THE PLASMA MEMBRANE OF CARDIOMYOCYTES

被引:92
作者
Balse, Elise
Steele, David F.
Abriel, Hugues
Coulombe, Alain
Fedida, David
Hatem, Stephane N.
机构
[1] Inst Cardiometab & Nutr, Paris, France
[2] Hop La Pitie Salpetriere, Assistance Publ Hop Paris, Heart & Metab Div, Paris, France
[3] Inst Natl Sante & Rech Med UMR S956, Paris, France
[4] Univ Paris 06, Paris, France
[5] Univ British Columbia, Dept Anesthesiol Pharmacol & Therapeut, Vancouver, BC V5Z 1M9, Canada
[6] Univ Bern, Dept Clin Res, Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
LONG-QT SYNDROME; VOLTAGE-GATED K+; TRANSMEMBRANE CONDUCTANCE REGULATOR; DUCHENNE MUSCULAR-DYSTROPHY; ADULT-RAT CARDIOMYOCYTES; RIGHT-VENTRICULAR CARDIOMYOPATHY; CLATHRIN-MEDIATED ENDOCYTOSIS; CARDIAC POTASSIUM CHANNEL; TUMOR-SUPPRESSOR PROTEIN; TRANS-GOLGI NETWORK;
D O I
10.1152/physrev.00041.2011
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Balse E, Steele DF, Abriel H, Coulombe A, Fedida D, Hatem SN. Dynamic of Ion Channel Expression at the Plasma Membrane of Cardiomyocytes. Physiol Rev 92: 1317-1358, 2012; doi:10.1152/physrev.00029.2011.-Cardiac myocytes are characterized by distinct structural and functional entities involved in the generation and transmission of the action potential and the excitation-contraction coupling process. Key to their function is the specific organization of ion channels and transporters to and within distinct membrane domains, which supports the anisotropic propagation of the depolarization wave. This review addresses the current knowledge on the molecular actors regulating the distinct trafficking and targeting mechanisms of ion channels in the highly polarized cardiac myocyte. In addition to ubiquitous mechanisms shared by other excitable cells, cardiac myocytes show unique specialization, illustrated by the molecular organization of myocyte-myocyte contacts, e. g., the intercalated disc and the gap junction. Many factors contribute to the specialization of the cardiac sarcolemma and the functional expression of cardiac ion channels, including various anchoring proteins, motors, small GTPases, membrane lipids, and cholesterol. The discovery of genetic defects in some of these actors, leading to complex cardiac disorders, emphasizes the importance of trafficking and targeting of ion channels to cardiac function. A major challenge in the field is to understand how these and other actors work together in intact myocytes to fine-tune ion channel expression and control cardiac excitability.
引用
收藏
页码:1317 / 1358
页数:42
相关论文
共 483 条
[1]   The anchoring protein SAP97 retains Kv1.5 channels in the plasma membrane of cardiac myocytes [J].
Abi-Char, Joelle ;
El-Haou, Said ;
Balse, Elise ;
Neyroud, Nathalie ;
Vranckx, Roger ;
Coulombe, Alain ;
Hatem, Stephane N. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2008, 294 (04) :H1851-H1861
[2]   Membrane cholesterol modulates Kv1.5 potassium channel distribution and function in rat cardiomyocytes [J].
Abi-Char, Joelle ;
Maguy, Ange ;
Coulombe, Alain ;
Balse, Elise ;
Ratajczak, Philippe ;
Samuel, Jane-Lise ;
Nattel, Stanley ;
Hatem, Stephane N. .
JOURNAL OF PHYSIOLOGY-LONDON, 2007, 582 (03) :1205-1217
[3]   Ubiquitylation of ion channels [J].
Abriel, H ;
Staub, O .
PHYSIOLOGY, 2005, 20 :398-407
[4]   Regulation of the cardiac voltage-gated Na+ channel (H1) by the ubiquitin-protein ligase Nedd4 [J].
Abriel, H ;
Kamynina, E ;
Horisberger, JD ;
Staub, O .
FEBS LETTERS, 2000, 466 (2-3) :377-380
[5]   Defective regulation of the epithelial Na+ channel by Nedd4 in Liddle's syndrome [J].
Abriel, H ;
Loffing, J ;
Rebhun, JF ;
Pratt, JH ;
Schild, L ;
Horisberger, JD ;
Rotin, D ;
Staub, O .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (05) :667-673
[6]   Seven novel mammalian SNARE proteins localize to distinct membrane compartments [J].
Advani, RJ ;
Bae, HR ;
Bock, JB ;
Chao, DS ;
Doung, YC ;
Prekeris, R ;
Yoo, JS ;
Scheller, RH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (17) :10317-10324
[7]   Modulation of the KV4.3 channel by syntaxin 1A [J].
Ahmed, Ishtlaq ;
Cosen-Binker, Laura I. ;
Leung, Yuk M. ;
Gaisano, Herbert Y. ;
Diamant, Nicholas E. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 358 (03) :789-795
[8]   Mechanisms underlying conduction slowing and arrhythmogenesis in nonischemic dilated cardiomyopathy [J].
Akar, FG ;
Spragg, DD ;
Tunin, RS ;
Kass, DA ;
Tomaselli, GF .
CIRCULATION RESEARCH, 2004, 95 (07) :717-725
[9]   Identification of the cyclic-nucleotide-binding domain as a conserved determinant of ion-channel cell-surface localization [J].
Akhavan, A ;
Atanasiu, R ;
Noguchi, T ;
Han, W ;
Holder, N ;
Shrier, A .
JOURNAL OF CELL SCIENCE, 2005, 118 (13) :2803-2812
[10]   Nedd4-2-dependent ubiquitylation and regulation of the cardiac potassium channel hERG1 [J].
Albesa, Maxime ;
Grilo, Liliana Sintra ;
Gavillet, Bruno ;
Abriel, Hugues .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2011, 51 (01) :90-98