Paracrine hypertrophic factors from cardiac non-myocyte cells downregulate the transient outward current density and Kv4.2 K+ channel expression in cultured rat cardiomyocytes

被引:17
作者
Guo, W
Kamiya, K
Yasui, K
Kodama, I
Toyama, J
机构
[1] Nagoya Univ, Dept Circulat, Environm Med Res Inst, Chikusa Ku, Nagoya, Aichi 4648601, Japan
[2] Nagoya Univ, Environm Med Res Inst, Div Regulat Organ Funct, Dept Humoral Regulat,Chikusa Ku, Nagoya, Aichi 4648601, Japan
关键词
hypertrophy; cardiomyocyte; cardiac non-myocyte cell; transient outward current; Shal;
D O I
10.1016/S0008-6363(98)00157-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Cardiac hypertrophy is characterized by a prolongation of action potential duration (APD) and a reduction of outward K+ currents, primarily the transient outward current (I-to). Since the interaction between cardiac non-myocyte cells (NMCs) and cardiomyocytes (MCs) plays a critical role during the process of myocardial hypertrophy, in the present study, we investigated the effects of NMCs on cell growth and K+ channel expression in cultured newborn rat ventricular cells. Methods: Single MCs were isolated from day-old Wistar rat ventricles and cultured for a period of five days. The effects of NMCs were examined by MC-NMC co-culture or incubating pure MCs in NMC-conditioned growth medium (NCGM). Whole-cell voltage-clamp recording and Western blot analysis using a polyclonal antibody against rat Kv4.2 channel protein were performed. Results: A marked increase in surface area and total cell protein concentration of MCs was observed in the MC-NMC co-culture. In the purl MC culture, this hypertrophic effect could be mimicked by a 72-h addition of NCGM, with a significant prolongation of APD(25) (APD at 25% repolarization) and a 42% decrease in I-to density (at +30 mV). The rates of inactivation and recovery from inactivation of I-to were unchanged. In the NCGM-treated MC culture, Western blots of MC proteins also showed a 36% reduction of the Kv4.2 K- channel protein level. In addition, the NCGM-induced MC hypertrophy was partially inhibited by anti-insulin-like growth factor-1 (IGF-1) antibody, while it revealed no effects on I-to density and Kv4.2 channel expression. Conclusions: These Endings first demonstrate that some paracrine hypertrophic factors released from cardiac NMCs, although unidentified, downregulate cardiac K+ channel expression. (C) 1999 Elsevier Science B.V. All rights reserved.
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页码:157 / 165
页数:9
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