OSCILLATING ACTIVITY OF A CALCIUM-ACTIVATED K+ CHANNEL IN NORMAL AND CANCEROUS MAMMARY CELLS IN CULTURE

被引:27
作者
ENOMOTO, KI
FURUYA, K
MAENO, T
EDWARDS, C
OKA, T
机构
[1] NIDDKD,MOLEC & CELL BIOL,BETHESDA,MD 20892
[2] NATL INST PHYSIOL SCI,DEPT CELLULAR PHYSIOL,OKAZAKI,AICHI 444,JAPAN
[3] UNIV S FLORIDA,COLL MED,TAMPA,FL 33612
关键词
CA-2+-ACTIVATED K+ CHANNEL; CA-2+ OSCILLATION; INWARD RECTIFICATION; CHARYBDOTOXIN; APAMIN;
D O I
10.1007/BF01871412
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Calcium-activated potassium channels were the channels most frequently observed in primary cultured normal mammary cell and in the established mammary tumor cell, MMT060562. In both cells, single-channel and whole-cell clamp recordings sometimes showed slow oscillations of the Ca2+-gated K+ current. The characteristics of the Ca2+-activated K+ channels in normal and cancerous mammary cells were quite similar. The slope conductances changed from 8 to 70 pS depending on the mode of recording and the ionic composition in the patch electrode. The open probability of this channel increased between 0.1 to 1 mu-M of the intracellular Ca2+, but it was independent of the membrane potential. Charybdotoxin reduced the activity of the Ca2+-activated K+ channel and the oscillation of the membrane current, but apamin had no apparent effect. The application of tetraethylammonium (TEA) from outside and BaCl2 from inside of the cell diminished the activity of the channel. The properties of this channel were different from those of both the large conductance (BK or MAXI K) and small conductance (SK) type Ca2+-activated K+ channels.
引用
收藏
页码:133 / 139
页数:7
相关论文
共 32 条
[31]  
YANG J, 1980, JNCI-J NATL CANCER I, V65, P337
[32]   SUSTAINED GROWTH AND 3-DIMENSIONAL ORGANIZATION OF PRIMARY MAMMARY-TUMOR EPITHELIAL-CELLS EMBEDDED IN COLLAGEN GELS [J].
YANG, J ;
RICHARDS, J ;
BOWMAN, P ;
GUZMAN, R ;
ENAMI, J ;
MCCORMICK, K ;
HAMAMOTO, S ;
PITELKA, D ;
NANDI, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (07) :3401-3405