ELECTROPHYSIOLOGICAL PROPERTIES OF NEONATAL MOUSE CARDIAC MYOCYTES IN PRIMARY CULTURE

被引:121
作者
NUSS, HB
MARBAN, E
机构
[1] Department of Medicine, Johns Hopkins University, Baltimore, Maryland
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1994年 / 479卷 / 02期
关键词
D O I
10.1113/jphysiol.1994.sp020294
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. The increasing utility of transgenic mice in molecular studies of the cardiovascular system has motivated us to characterize the ionic currents in neonatal mouse ventricular myocytes. 2. Cell capacitance measurements (30 +/- 1 pF, n = 73) confirmed visual impressions that neonatal mouse ventricular myocytes in primary culture are considerably smaller than freshly isolated adult ventricular myocytes. With the use of electron microscopy, mitochondria and sarcoplasmic reticulum were found in close association with myofibrils, but transverse tubules were not observed. 3. Action potential durations, measured at 50 and 90% repolarization, were 23 +/- 1 and 42 +/- 2 ms respectively (n = 46). Application of 4-aminopyridine (4-AP; 5 mM) prolonged action potential duration at 50% repolarization by 26 +/- 5% (n = 3). The brevity of the action potential is explained by the rapid activation of a transient outward K+ current upon voltage-clamp depolarization to plateau potentials. 4. Potassium currents identified include an inward rectifier, a large 4-AP-sensitive transient outward, a slowly inactivating 4-AP-insensitive outward, a slowly activating delayed rectifier and a small rapidly activating E-4031 (10 mu M)-sensitive delayed rectifier K+ current. 5. Sodium currents (-305 +/- 50 pA pF(-1), n = 21) were recorded in 40 mM Na+ with Ni2+ (1 mM) to block Ca2+ currents and with K+ replaced by Cs+. The relative insensitivity of the Na+ current to block by tetrodotoxin (IC50 = 2.2 +/- 0.3 mu M, n = 4) is distinctive of the cardiac Na+ channel isoform. 6. Nitrendipine-insensitive (10 mu M) Ba2+ currents elicited during steps from -90 to -30 mV measured -25 +/- 5 pA pF(-1) (n = 7, 30 mM Ba2+). Decay of these currents was complete during 180 ms depolarizations, even with Ba2+ as the charge carrier. These currents were not present when the holding potential was set at -50 mV. These data support the presence of a low threshold, T-type Ca2+ current. 7. The maximal nitrendipine-sensitive L-type Ca2+ current density was -10 + 2 pA pF(-1) (n = 8) in 2 mM Ca2+ and -38 +/- 5 pA pF(-1) (n = 9) in 30 mM Ba2+. Exposure to isoprenaline (1 mu M) resulted in an 82% increase (n = 3) in the amplitude of the Ba2+ currents elicited at 0 mV. 8. Neonatal mouse cardiac myocytes in primary culture possess surprisingly large inward currents given the brevity of their action potentials. Their small cell size and apparent absence of transverse tubules makes them technically favourable for whole-cell patch clamp studies. For these reasons, this preparation promises to be useful for the phenotypic characterization of transgenic mice.
引用
收藏
页码:265 / 279
页数:15
相关论文
共 40 条
[1]   COMPARISON OF THE NUMBER OF DIHYDROPYRIDINE RECEPTORS WITH THE NUMBER OF FUNCTIONAL L-TYPE CALCIUM CHANNELS IN EMBRYONIC HEART [J].
AIBA, S ;
CREAZZO, TL .
CIRCULATION RESEARCH, 1993, 72 (02) :396-402
[2]   TRANSGENIC MICE [J].
BABINET, C ;
MORELLO, D ;
RENARD, JP .
GENOME, 1989, 31 (02) :938-949
[3]   MACROSCOPIC AND UNITARY PROPERTIES OF PHYSIOLOGICAL ION FLUX THROUGH T-TYPE CA2+ CHANNELS IN GUINEA-PIG HEART-CELLS [J].
BALKE, CW ;
ROSE, WC ;
MARBAN, E ;
WIER, WG .
JOURNAL OF PHYSIOLOGY-LONDON, 1992, 456 :247-265
[4]   2 KINDS OF CALCIUM CHANNELS IN CANINE ATRIAL CELLS - DIFFERENCES IN KINETICS, SELECTIVITY AND PHARMACOLOGY [J].
BEAN, BP .
JOURNAL OF GENERAL PHYSIOLOGY, 1985, 86 (01) :1-30
[5]  
BENNDORF K, 1988, BIOMED BIOCHIM ACTA, V47, P401
[6]   SODIUM CURRENT IN SINGLE MYOCARDIAL MOUSE CELLS [J].
BENNDORF, K ;
BOLDT, W ;
NILIUS, B .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1985, 404 (02) :190-196
[7]  
BENNDORF K, 1988, GEN PHYSIOL BIOPHYS, V7, P353
[8]   VENTRICULAR ELECTROPHYSIOLOGICAL PROPERTIES - IS INTERSPECIES VARIABILITY RELATED TO THYROID STATE [J].
BINAH, O ;
ARIELI, R ;
BECK, R ;
ROSEN, MR ;
PALTI, Y .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 252 (06) :H1265-H1274
[9]   COMPARATIVE STEREOLOGY OF THE MOUSE AND FINCH LEFT-VENTRICLE [J].
BOSSEN, EH ;
SOMMER, JR ;
WAUGH, RA .
TISSUE & CELL, 1978, 10 (04) :773-784
[10]  
CAMPBELL DL, 1993, J GEN PHYSIOL, V101, P571, DOI 10.1085/jgp.101.4.571