Expression and function of dipeptidyl-aminopeptidase-like protein 6 as a putative β-subunit of human cardiac transient outward current encoded by Kv4.3

被引:92
作者
Radicke, S [1 ]
Cotella, D [1 ]
Graf, EM [1 ]
Ravens, U [1 ]
Wettwer, E [1 ]
机构
[1] Tech Univ Dresden, Fac Med, Dept Pharmacol & Toxicol, D-01307 Dresden, Germany
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2005年 / 565卷 / 03期
关键词
D O I
10.1113/jphysiol.2005.087312
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Dipeptidyl-aminopeptidase-like protein 6 (DPPX) was recently shown in the brain to modulate the kinetics of transient A-type currents by accelerating inactivation and recovery from inactivation. Since the kinetics of human cardiac transient outward current (It.) are not mimicked by coexpression of the a-subunit Kv4.3 with its known, beta-subunit KChIP2, we have tested the hypothesis that DPPX may serve as an additional beta-subunit in the human heart. With quantitative real-time RT-PCR strong mRNA expression of DPPX was detected in human ventricles and was verified at the protein level in human but not in rat heart by a DPPX-specific antibody. Co-expression of DPPX with Kv4.3 in Chinese hamster ovary cells produced I-to-like currents, but compared with expression of KChIP2a and Kv4.3, the time constant of inactivation was faster, the potential of half-maximum steady-state inactivation was more negative and recovery from inactivation was delayed. Co-expression of DPPX in addition to Kv4.3 and KChIP2a produced similar current kinetics as in human ventricular myocytes. We therefore propose that DPPX is an essential component of the native cardiac I-to channel complex in human heart.
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收藏
页码:751 / 756
页数:6
相关论文
共 14 条
[1]   Modulation of Kv4.3 current by accessory subunits [J].
Deschênes, I ;
Tomaselli, GF .
FEBS LETTERS, 2002, 528 (1-3) :183-188
[2]   Role of the Kv4.3 K+ channel in ventricular muscle - A molecular correlate for the transient outward current [J].
Dixon, JE ;
Shi, WM ;
Wang, HS ;
McDonald, C ;
Yu, H ;
Wymore, RS ;
Cohen, IS ;
McKinnon, D .
CIRCULATION RESEARCH, 1996, 79 (04) :659-668
[3]   KCNE2 protein is expressed in ventricles of different species, and changes in its expression contribute to electrical remodeling in diseased hearts [J].
Jiang, M ;
Zhang, M ;
Tang, DG ;
Clemo, HF ;
Liu, J ;
Holwitt, D ;
Kasirajan, V ;
Pond, AL ;
Wettwer, E ;
Tseng, GN .
CIRCULATION, 2004, 109 (14) :1783-1788
[4]   Molecular basis of transient outward potassium current downregulation in human heart failure -: A decrease in Kv4.3 mRNA correlates with a reduction in current density [J].
Kääb, S ;
Dixon, J ;
Duc, J ;
Ashen, D ;
Näbauer, M ;
Beuckelmann, DJ ;
Steinbeck, G ;
McKinnon, D ;
Tomaselli, GF .
CIRCULATION, 1998, 98 (14) :1383-1393
[5]   Biosynthesis and characterization of the brain-specific membrane protein DPPX, a dipeptidyl peptidase IV-related protein [J].
Kin, Y ;
Misumi, Y ;
Ikehara, Y .
JOURNAL OF BIOCHEMISTRY, 2001, 129 (02) :289-295
[6]  
KLOOS P, 2005, Z KARDIOL S1, V94, pV274
[7]   The CD26-related dipeptidyl aminopeptidase-like protein DPPX is a critical component of neuronal A-type K+ channels [J].
Nadal, MS ;
Ozaita, A ;
Amarillo, Y ;
Vega-Saenz de Miera, E ;
Ma, YL ;
Mo, WJ ;
Goldberg, EM ;
Misumi, Y ;
Ikehara, Y ;
Neubert, TA ;
Rudy, B .
NEURON, 2003, 37 (03) :449-461
[8]   Properties, expression and potential roles of cardiac K+ channel accessory subunits:: MinK, MiRPs, KChIP, and KChAP [J].
Pourrier, M ;
Schram, G ;
Nattel, S .
JOURNAL OF MEMBRANE BIOLOGY, 2003, 194 (03) :141-152
[9]  
Sambrook J, 2001, MOL CLONING LAB MANU, DOI DOI 10.1016/0003-2697(90)90595-Z
[10]   A fundamental role for KChIPs in determining the molecular properties and trafficking of Kv4.2 potassium channels [J].
Shibata, R ;
Misonou, H ;
Campomanes, CR ;
Anderson, AE ;
Schrader, LA ;
Doliveira, LC ;
Carroll, KI ;
Sweatt, JD ;
Rhodes, KJ ;
Trimmer, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (38) :36445-36454