Propagation of mechanically induced intercellular calcium waves via gap junctions and ATP receptors in rat liver epithelial cells

被引:82
作者
Frame, MK
deFeijter, AW
机构
[1] Meridian Instruments, Inc., Okemos
[2] Meridian Instruments, Inc., Okemos, MI 48864
关键词
D O I
10.1006/excr.1996.3409
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mechanical stimulation was used to initiate Ca2+ waves in rat liver epithelial cells in order to ascertain the degree to which gap junctional intercellular communication (GJIC) is involved in communication of Ca2+ to adjacent cells and to assess alternative C2+ signaling pathways that may be present between these cells. In both WB-F344 cells, which show a high degree of GJIC, and WB-aB1 cells, which are GJIC deficient, mechanical stimulation of a single cell induced a Ca2+ wave which propagated away from the point of stimulation, across cell borders, to neighboring cells directly or indirectly in contact with the stimulated cell. In addition, the Ca2+ wave was transmitted to nearby isolated cells that exhibited no direct or indirect contact with the stimulated cell. Treatment of cells with 18 beta-glycyrrhetinic acid, a compound that has been shown to block GJIC, did not significantly affect propagation of the Ca2+ wave. In contrast, treatment with suramin, a P-2-purinergic receptor inhibitor, significantly reduced both the rate and the extent of Ca2+ wave propagation in WB-F344 cells and completely blocked its propagation in WB-aB1 cells. Cotreatment with suramin and glycyrrhetinic acid was found to completely block the mechanically induced Ca2+ wave in both cell lines. These studies indicate that mechanically induced cell injury in rat liver epithelial cells initiates signaling through at least two pathways, involving intercellular communication via gap junctions and extracellular communication via ATP activation of purinergic receptors. (C) 1997 Academic Press.
引用
收藏
页码:197 / 207
页数:11
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共 50 条
[1]   RAPID AND REVERSIBLE REDUCTION OF JUNCTIONAL PERMEABILITY IN CELLS INFECTED WITH A TEMPERATURE-SENSITIVE MUTANT OF AVIAN-SARCOMA VIRUS [J].
ATKINSON, MM ;
MENKO, AS ;
JOHNSON, RG ;
SHEPPARD, JR ;
SHERIDAN, JD .
JOURNAL OF CELL BIOLOGY, 1981, 91 (02) :573-578
[2]  
BOITANO S, 1994, J CELL SCI, V107, P3037
[3]   INTERCELLULAR PROPAGATION OF CALCIUM WAVES MEDIATED BY INOSITOL TRISPHOSPHATE [J].
BOITANO, S ;
DIRKSEN, ER ;
SANDERSON, MJ .
SCIENCE, 1992, 258 (5080) :292-295
[4]   THE ELEMENTAL PRINCIPLES OF CALCIUM SIGNALING [J].
BOOTMAN, MD ;
BERRIDGE, MJ .
CELL, 1995, 83 (05) :675-678
[5]   CELL-CULTURE ASSAYS FOR CHEMICALS WITH TUMOR-PROMOTING OR TUMOR-INHIBITING ACTIVITY-BASED ON THE MODULATION OF INTERCELLULAR COMMUNICATION [J].
BUDUNOVA, IV ;
WILLIAMS, GM .
CELL BIOLOGY AND TOXICOLOGY, 1994, 10 (02) :71-116
[6]   INTERCELLULAR SIGNALING IN GLIAL-CELLS - CALCIUM WAVES AND OSCILLATIONS IN RESPONSE TO MECHANICAL STIMULATION AND GLUTAMATE [J].
CHARLES, AC ;
MERRILL, JE ;
DIRKSEN, ER ;
SANDERSON, MJ .
NEURON, 1991, 6 (06) :983-992
[7]   MECHANISMS OF INTERCELLULAR CALCIUM SIGNALING IN GLIAL-CELLS STUDIED WITH DANTROLENE AND THAPSIGARGIN [J].
CHARLES, AC ;
DIRKSEN, ER ;
MERRILL, JE ;
SANDERSON, MJ .
GLIA, 1993, 7 (02) :134-145
[8]   INTERCELLULAR CALCIUM SIGNALING VIA GAP-JUNCTIONS IN GLIOMA-CELLS [J].
CHARLES, AC ;
NAUS, CCG ;
ZHU, DG ;
KIDDER, GM ;
DIRKSEN, ER ;
SANDERSON, MJ .
JOURNAL OF CELL BIOLOGY, 1992, 118 (01) :195-201
[9]   CALCIUM SIGNALING [J].
CLAPHAM, DE .
CELL, 1995, 80 (02) :259-268
[10]  
DAVIDSON JS, 1988, J PHARMACOL EXP THER, V246, P1104