Osmosensitivity of the hyperpolarization-activated chloride current in human intestinal T84 cells

被引:32
作者
Fritsch, J
Edelman, A
机构
[1] HOP NECKER ENFANTS MALAD, CNRS URA 583, LAB CALCIUM & TISSU OSSEUX ORGANISME DEV, F-75015 PARIS, FRANCE
[2] CHU NECKER, INSERM U467, LAB PHYSIOL & BIOPHYS SYST TRANSPORT, F-75015 PARIS, FRANCE
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1997年 / 272卷 / 03期
关键词
volume regulated; ClC-2;
D O I
10.1152/ajpcell.1997.272.3.C778
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The osmosensitivity of the hyperpolarization-activated chloride current (I-Clhyp) in T84 cells was studied using the whole cell patch-clamp recording configuration. Hypotonicity is known to activate an outwardly rectify ing chloride current (HIORC) distinct from I-Clhyp in these cells. The differing sensitivities of HIORC and I-Clhyp, toward inhibitors (1,9-dideoxyforskolin blocked HIORC but not I-Clhyp, and Cd2+ inhibited I-Clhyp but not HIORC) allowed us to investigate the osmoregulation of I-Clhyp. Hypotonicity induced an increase in I-Clhyp amplitude. Protein phosphatase inhibitors prevented this effect, and hypotonic solutions became slightly inhibitory. Hypertonicity resulted in a transient increase in I-Clhyp amplitude followed by a large decrease. The complex responses of I-Clhyp to osmotic changes indicate that these signals affect the same channel via multiple transduction pathways. The responses of I-Clhyp to hypotonicity have features in common with the responses of ClC-2 channels expressed in Xenopus oocytes (activation) and with hyperpolarization-activated chloride currents in other cell types, such as osteoblasts and mandibular duct cells (inhibition).
引用
收藏
页码:C778 / C786
页数:9
相关论文
共 28 条
[1]  
CHESNOYMARCHAIS D, 1994, J MEMBRANE BIOL, V140, P173
[2]   CLONING OF A PUTATIVE HUMAN VOLTAGE-GATED CHLORIDE CHANNEL (CIC-2) CDNA WIDELY EXPRESSED IN HUMAN TISSUES [J].
CID, LP ;
MONTROSERAFIZADEH, C ;
SMITH, DI ;
GUGGINO, WB ;
CUTTING, GR .
HUMAN MOLECULAR GENETICS, 1995, 4 (03) :407-413
[3]   THE STRUCTURE AND REGULATION OF PROTEIN PHOSPHATASES [J].
COHEN, P .
ANNUAL REVIEW OF BIOCHEMISTRY, 1989, 58 :453-508
[4]   VOLUME-ACTIVATED CHLORIDE CHANNELS IN HELA-CELLS ARE BLOCKED BY VERAPAMIL AND DIDEOXYFORSKOLIN [J].
DIAZ, M ;
VALVERDE, MA ;
HIGGINS, CF ;
RUCAREANU, C ;
SEPULVEDA, FV .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1993, 422 (04) :347-353
[5]   Modulation of the hyperpolarization-activated Cl- current in human intestinal T-84 epithelial cells by phosphorylation [J].
Fritsch, J ;
Edelman, A .
JOURNAL OF PHYSIOLOGY-LONDON, 1996, 490 (01) :115-128
[6]  
Grinstein Sergio, 1992, News in Physiological Sciences, V7, P232
[7]   REGIONS INVOLVED IN THE OPENING OF CIC-2 CHLORIDE CHANNEL BY VOLTAGE AND CELL-VOLUME [J].
GRUNDER, S ;
THIEMANN, A ;
PUSCH, M ;
JENTSCH, TJ .
NATURE, 1992, 360 (6406) :759-762
[8]   MEMBRANE MECHANISMS IN VOLUME AND PH REGULATION IN VERTEBRATE CELLS [J].
HOFFMANN, EK ;
SIMONSEN, LO .
PHYSIOLOGICAL REVIEWS, 1989, 69 (02) :315-382
[9]   CALYCULIN-A AND OKADAIC ACID - INHIBITORS OF PROTEIN PHOSPHATASE-ACTIVITY [J].
ISHIHARA, H ;
MARTIN, BL ;
BRAUTIGAN, DL ;
KARAKI, H ;
OZAKI, H ;
KATO, Y ;
FUSETANI, N ;
WATABE, S ;
HASHIMOTO, K ;
UEMURA, D ;
HARTSHORNE, DJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 159 (03) :871-877
[10]   OKADAIC ACID INHIBITION OF KCL COTRANSPORT - EVIDENCE THAT PROTEIN DEPHOSPHORYLATION IS NECESSARY FOR ACTIVATION OF TRANSPORT BY EITHER CELL SWELLING OR N-ETHYLMALEIMIDE [J].
JENNINGS, ML ;
SCHULZ, RK .
JOURNAL OF GENERAL PHYSIOLOGY, 1991, 97 (04) :799-818