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超极化激活的非选择性阳离子电流I(f)在永生化HL-1心肌细胞中的功能性表达。

Functional expression of the hyperpolarization-activated, non-selective cation current I(f) in immortalized HL-1 cardiomyocytes.

作者信息

Sartiani Laura, Bochet Pascal, Cerbai Elisabetta, Mugelli Alessandro, Fischmeister Rodolphe

机构信息

Department of Preclinical and Clinical Pharmacology, University of Firenze, 50139 Florence, Italy.

出版信息

J Physiol. 2002 Nov 15;545(1):81-92. doi: 10.1113/jphysiol.2002.021535.

Abstract

HL-1 cells are adult mouse atrial myocytes induced to proliferate indefinitely by SV40 large T antigen. These cells beat spontaneously when confluent and express several adult cardiac cell markers including the outward delayed rectifier K(+) channel. Here, we examined the presence of a hyperpolarization-activated I(f) current in HL-1 cells using the whole-cell patch-clamp technique on isolated cells enzymatically dissociated from the culture at confluence. Cell membrane capacitance (C(m)) ranged from 5 to 53 pF. I(f) was detected in about 30% of the cells and its occurrence was independent of the stage of the culture. I(f) maximal slope conductance was 89.7 +/- 0.4 pS pF(-1) (n = 10). I(f) current in HL-1 cells showed typical characteristics of native cardiac I(f) current: activation threshold between -50 and -60 mV, half-maximal activation potential of -83.1 +/- 0.7 mV (n = 50), reversal potential at -20.8 +/- 1.5 mV (n = 10), time-dependent activation by hyperpolarization and blockade by 4 mM Cs(+). In half of the cells tested, activation of adenylyl cyclase by the forskolin analogue L858051 (20 microM) induced both an approximately 6 mV positive shift of the half-activation potential and an approximately 37 % increase in the fully activated I(f) current. RT-PCR analysis of the hyperpolarization-activated, cyclic nucleotide-gated channels (HCN) expressed in HL-1 cells demonstrated major contributions of HCN1 and HCN2 channel isoforms to I(f) current. Cytosolic Ca(2+) oscillations in spontaneously beating HL-1 cells were measured in Fluo-3 AM-loaded cells using a fast-scanning confocal microscope. The oscillation frequency ranged from 1.3 to 5 Hz and the spontaneous activity was stopped in the presence of 4 mM Cs(+). Action potentials from HL-1 cells had a triangular shape, with an overshoot at +15 mV and a maximal diastolic potential of -69 mV, i.e. more negative than the threshold potential for I(f) activation. In conclusion, HL-1 cells display a hyperpolarization-activated I(f) current which might contribute to the spontaneous contractile activity of these cells.

摘要

HL-1细胞是由SV40大T抗原诱导而能无限增殖的成年小鼠心房肌细胞。这些细胞汇合时会自发搏动,并表达多种成年心脏细胞标志物,包括外向延迟整流钾(K⁺)通道。在此,我们使用全细胞膜片钳技术,对汇合培养时酶解分离得到的单个HL-1细胞进行检测,以研究HL-1细胞中是否存在超极化激活的I(f)电流。细胞膜电容(C(m))范围为5至53皮法。约30%的细胞检测到I(f)电流,其出现与培养阶段无关。I(f)的最大斜率电导为89.7±0.4皮西门子/皮法⁻¹(n = 10)。HL-1细胞中的I(f)电流表现出天然心脏I(f)电流的典型特征:激活阈值在-50至-60毫伏之间,半最大激活电位为-83.1±0.7毫伏(n = 50),反转电位为-20.8±1.5毫伏(n = 10),通过超极化产生时间依赖性激活,并被4毫摩尔/升的铯(Cs⁺)阻断。在一半的测试细胞中,福司可林类似物L858051(20微摩尔)激活腺苷酸环化酶后,半激活电位出现约6毫伏的正向偏移,完全激活的I(f)电流增加约37%。对HL-1细胞中表达的超极化激活的环核苷酸门控通道(HCN)进行逆转录聚合酶链反应(RT-PCR)分析表明,HCN1和HCN2通道亚型对I(f)电流起主要作用。使用快速扫描共聚焦显微镜,在负载Fluo-3 AM的自发搏动的HL-1细胞中测量胞质Ca²⁺振荡。振荡频率范围为1.3至5赫兹,在4毫摩尔/升Cs⁺存在时自发活动停止。HL-1细胞的动作电位呈三角形,在+15毫伏处有超射,最大舒张电位为-69毫伏,即比I(f)激活的阈值电位更负。总之,HL-1细胞表现出超极化激活的I(f)电流,这可能有助于这些细胞的自发收缩活动。

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