Excitatory sodium currents of NH15-CA2 neuroblastoma x glioma hybrid cells are differently affected by interleukin-2 and interleukin-1 beta

被引:7
作者
Hamm, S [1 ]
Rudel, R [1 ]
Brinkmeier, H [1 ]
机构
[1] UNIV ULM,ALLGEMEINE PHYSIOL ABT,D-89069 ULM,GERMANY
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 1996年 / 433卷 / 1-2期
关键词
interleukin-1; beta; interleukin-2; neuronal Na+ channels; neuroblastoma x glioma cell line; NH15-CA2; inflammatory neurological disease;
D O I
10.1007/s004240050262
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The neuroblastoma x glioma hybrid cell. line NH15-CA2 was used to test the effects of two interleukins on neuronal Na+ channels. The cells were cultured in the presence of dibutyryl cAMP and retinoic acid, which yielded a high expression of Na+ channels so that the cells were excitable. Na+ currents were triggered and recorded in the whole-cell recording mode. Comparison of the effects of tetrodotoxin and mu-conotoxin established that the expressed Na+ channels were of the neuronal type. Bath-applied recombinant human interleukin-2 (rIL-2) had a reversible inhibitory effect on the Na+ currents, although to a lesser extent than on muscular Na+ currents (more than 1000 U/ml required for 50% block in NH15-CA2 cells vs 500 U/ml in myoballs). The current/voltage relationship was not affected by the presence of rIL-2, but the steady-state inactivation curve was shifted by -7.7 +/- 4.8 mV (mean +/- SD, n=18). Recombinant human interleukin-1 beta (rIL-1 beta), applied at 1000 U/ml, showed an inhibitory effect on the Na+ currents in about one-third of the cells tested. The mechanism of inhibition was different from that of rIL-2, as rIL-1 beta seemed to cause a block without affecting voltage dependence or kinetics of the channels.
引用
收藏
页码:160 / 165
页数:6
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