Chloride conductance determining membrane potential of rabbit articular chondrocytes

被引:38
作者
Tsuga, K
Tohse, N
Yoshino, M
Sugimoto, T
Yamashita, T
Ishii, S
Yabu, H
机构
[1] Sapporo Med Univ, Sch Med, Dept Physiol, Chuo Ku, Sapporo, Hokkaido 0608556, Japan
[2] Sapporo Med Univ, Sch Med, Dept Orthopaed Surg, Chuo Ku, Sapporo, Hokkaido 0608556, Japan
关键词
chloride channel; membrane potential; articular chondrocytes; SITS; patch clamp; rabbit;
D O I
10.1007/s00232-001-0112-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Membrane conductance of cultured rabbit articular chondrocytes was characterized by means of the patch-clamp technique. The resting membrane potential of the articular chondrocytes was about -42 mV. The membrane potential shifted in accordance with the prediction by the Nernst equation for Cl(-)when intracellular and extracellular concentrations of Cl- were changed. On the other hand, change in extracellular concentration of K+ produced no shift in the membrane potential of chondrocytes. The Cl(-)channel blocker 4-acetamido-4-isothiocyanatostilbene-2'2-disulfonic acid (SITS) depolarized the membrane potential. These findings suggest that the membrane potential of the chondrocytes is determined mainly by Cl- conductance. Using the cell-attached patch-clamp method, a large unitary conductance of 217 pS was observed in the articular chondrocytes. The unitary current was reversibly blocked by SITS. Therefore, the unitary current was carried by Cl-. The Cl- channel showed voltage-dependent activation and the channels exhibited longlasting openings. Therefore, the membrane potential of rabbit cultured articular chondrocytes was mainly determined by the activities of the large-conductance and voltage-dependent Cl- channels.
引用
收藏
页码:75 / 81
页数:7
相关论文
共 25 条
[1]
AICKIN CC, 1990, CHLORIDE CHANNELS AND CARRIERS IN NERVE, MUSCLE, AND GLIAL CELLS, P209
[2]
INTRACELLULAR CHLORIDE REGULATION IN AMPHIBIAN DORSAL-ROOT GANGLION NEURONS STUDIED WITH ION-SELECTIVE MICROELECTRODES [J].
ALVAREZLEEFMANS, FJ ;
GAMINO, SM ;
GIRALDEZ, F ;
NOGUERON, I .
JOURNAL OF PHYSIOLOGY-LONDON, 1988, 406 :225-246
[3]
SINGLE VOLTAGE-DEPENDENT CHLORIDE-SELECTIVE CHANNELS OF LARGE CONDUCTANCE IN CULTURED RAT MUSCLE [J].
BLATZ, AL ;
MAGLEBY, KL .
BIOPHYSICAL JOURNAL, 1983, 43 (02) :237-241
[4]
ELECTROPHYSIOLOGY OF A CLONAL OSTEOBLAST-LIKE CELL-LINE - EVIDENCE FOR THE EXISTENCE OF A CA-2+-ACTIVATED K+ CONDUCTANCE [J].
DIXON, SJ ;
AUBIN, JE ;
DAINTY, J .
JOURNAL OF MEMBRANE BIOLOGY, 1984, 80 (01) :49-58
[5]
FREEDMAN JC, 1998, CELL PHYSL SOURCE BO, P325
[6]
FRITSCH J, 1987, BONE MINER, V2, P463
[7]
CALCIUM-ACTIVATED POTASSIUM CHANNELS IN CHONDROCYTES [J].
GRANDOLFO, M ;
DANDREA, P ;
MARTINA, M ;
RUZZIER, F ;
VITTUR, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 182 (03) :1429-1434
[8]
A POTASSIUM CHANNEL IN CULTURED CHONDROCYTES [J].
GRANDOLFO, M ;
MARTINA, M ;
RUZZIER, F ;
VITTUR, F .
CALCIFIED TISSUE INTERNATIONAL, 1990, 47 (05) :302-307
[9]
HIGH CONDUCTANCE ANION-SELECTIVE CHANNELS IN RAT CULTURED SCHWANN-CELLS [J].
GRAY, PTA ;
BEVAN, S ;
RITCHIE, JM .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1984, 221 (1225) :395-409
[10]
The cellular physiology of articular cartilage [J].
Hall, AC ;
Horwitz, ER ;
Wilkins, RJ .
EXPERIMENTAL PHYSIOLOGY, 1996, 81 (03) :535-545