HGF/SF INHIBITS JUNCTIONAL COMMUNICATION

被引:37
作者
MOORBY, CD
STOKER, M
GHERARDI, E
机构
[1] Cell Interactions Laboratory, Cambridge University Medical School, MRC Centre, Cambridge
关键词
D O I
10.1006/excr.1995.1276
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocyte growth factor/scatter factor (HGF/SF) is a fibroblast-derived protein that affects the growth, motility, and differentiation of epithelial and endothelial cells. We have investigated the effect of HGF/SF on junctional communication in mouse keratinocytes (MK cells). HGF/SF inhibited cell communication in MK cells as assessed by the transfer of a low-molecular-weight dye, Lucifer Yellow, The inhibition was rapid, the earliest effects being apparent 5 to 10 min after addition of the factor, and was transient. The decrease in dye transfer correlated with a loss of the gap junction protein connexin 43 as measured by Western blotting, probably due to increased protein degradation. The results show that junctional communication is an early target of HGF/SF activity and they are consistent with the hypothesis that gap junctions are primary targets of the action of growth factors. (C) 1995 Academic Press, Inc.
引用
收藏
页码:657 / 663
页数:7
相关论文
共 31 条
[1]  
BENNETT MVL, 1991, NEURON, V6, P305, DOI 10.1016/0896-6273(91)90241-Q
[2]  
BERTHOUD VM, 1992, EUR J CELL BIOL, V57, P40
[3]   CONNEXIN FAMILY OF GAP JUNCTION PROTEINS [J].
BEYER, EC ;
PAUL, DL ;
GOODENOUGH, DA .
JOURNAL OF MEMBRANE BIOLOGY, 1990, 116 (03) :187-194
[4]   IDENTIFICATION OF THE HEPATOCYTE GROWTH-FACTOR RECEPTOR AS THE C-MET PROTOONCOGENE PRODUCT [J].
BOTTARO, DP ;
RUBIN, JS ;
FALETTO, DL ;
CHAN, AML ;
KMIECIK, TE ;
VANDEWOUDE, GF ;
AARONSON, SA .
SCIENCE, 1991, 251 (4995) :802-804
[5]   HEPATOCYTES AND SCATTER FACTOR [J].
GHERARDI, E ;
STOKER, M .
NATURE, 1990, 346 (6281) :228-228
[6]   PURIFICATION OF SCATTER FACTOR, A FIBROBLAST-DERIVED BASIC-PROTEIN THAT MODULATES EPITHELIAL INTERACTIONS AND MOVEMENT [J].
GHERARDI, E ;
GRAY, J ;
STOKER, M ;
PERRYMAN, M ;
FURLONG, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (15) :5844-5848
[7]  
GHERARDI E, 1993, SYM SOC EXP BIOL, V47, P163
[8]   LYSOPHOSPHATIDIC ACID INHIBITS GAP-JUNCTIONAL COMMUNICATION AND STIMULATES PHOSPHORYLATION OF CONNEXIN-43 IN WB CELLS - POSSIBLE INVOLVEMENT OF THE MITOGEN-ACTIVATED PROTEIN-KINASE CASCADE [J].
HII, CST ;
OH, SY ;
SCHMIDT, SA ;
CLARK, KJ ;
MURRAY, AW .
BIOCHEMICAL JOURNAL, 1994, 303 :475-479
[9]   TURNOVER AND PHOSPHORYLATION DYNAMICS OF CONNEXIN43 GAP JUNCTION PROTEIN IN CULTURED CARDIAC MYOCYTES [J].
LAIRD, DW ;
PURANAM, KL ;
REVEL, JP .
BIOCHEMICAL JOURNAL, 1991, 273 :67-72
[10]   EPIDERMAL GROWTH-FACTOR DISRUPTS GAP-JUNCTIONAL COMMUNICATION AND INDUCES PHOSPHORYLATION OF CONNEXIN43 ON SERINE [J].
LAU, AF ;
KANEMITSU, MY ;
KURATA, WE ;
DANESH, S ;
BOYNTON, AL .
MOLECULAR BIOLOGY OF THE CELL, 1992, 3 (08) :865-874