2 INHIBITORS OF GAP JUNCTIONAL INTERCELLULAR COMMUNICATION, TPA AND ENDOSULFAN - DIFFERENT EFFECTS ON PHOSPHORYLATION OF CONNEXIN-43 IN THE RAT-LIVER EPITHELIAL-CELL LINE, IAR 20

被引:47
作者
KENNE, K
FRANSSONSTEEN, R
HONKASALO, S
WARNGARD, L
机构
[1] Institute of Environmental Medicine, S-171 77 Stockholm
关键词
D O I
10.1093/carcin/15.6.1161
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The skin tumour promoter 12-O-tetradecanoylphorbol-13-acetate (TPA) and the chlorinated insecticide, endosulfan, are two potent inhibitors of gap junctional intercellular communication. In the present study the effects of TPA and endosulfan on cell communication have been investigated in IAR 20 rat liver epithelial cells, as well as the effects of these compounds on connexin 43 (cx43), the main gap junction protein in this cell line. The results clearly demonstrate that at non-toxic doses both compounds inhibited the cell communication by at least 90% within 5 min. The communication was partially restored after 4 h of TPA exposure and almost fully restored by 24 h, whereas in endosulfan-exposed cells the communication was completely down-regulated for the whole exposure-period of 24 h. Immunoblots of IAR 20 cell extracts indicated that TPA initially caused an increased phosphorylation of cx43. A normal phosphorylation pattern was observed after 4 h when the cell communication was restored. Immunoblot analysis after endosulfan-exposure showed a slightly increased phosphorylation of cx43 after 10 min treatment, gradually followed by dephosphorylation during the rest of the 24 h treatment period. Immunostaining of IAR 20 cells showed that both compounds caused a rapid disappearance of cx43 from the cell membrane. After 4 h of exposure immunofluorescent cx43-plaques started to reappear in the cell membrane, although less pronounced in endosulfan-treated cells. However, after 24 h of endosulfan-exposure a high number of cx43-spots was demonstrated. These results indicate that different mechanisms are responsible for the inhibition of gap junctional intercellular communication induced by TPA and by endosulfan, at least during the later part of the 24 h exposure-period. TPA causes a marked hyperphosphorylation of cx43, whereas endosulfan increases phosphorylation initially only slightly but longer exposure-periods lead to hypophosphorylation. Thus, phosphorylation as well as dephosphorylation seem to be important factors involved in the regulation of the function of cx43 in this cell line.
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页码:1161 / 1165
页数:5
相关论文
共 36 条
[1]   MOLECULAR MECHANISMS OF TPA-MEDIATED INHIBITION OF GAP-JUNCTIONAL INTERCELLULAR COMMUNICATION - EVIDENCE FOR ACTION ON THE ASSEMBLY OR FUNCTION BUT NOT THE EXPRESSION OF CONNEXIN 43 IN RAT-LIVER EPITHELIAL-CELLS [J].
ASAMOTO, M ;
OYAMADA, M ;
ELAOUMARI, A ;
GROS, D ;
YAMASAKI, H .
MOLECULAR CARCINOGENESIS, 1991, 4 (04) :322-327
[2]  
BENNETT MVL, 1991, NEURON, V6, P305, DOI 10.1016/0896-6273(91)90241-Q
[3]  
BERTHOUD VM, 1992, EUR J CELL BIOL, V57, P40
[4]   THE TUMOR PROMOTER 12-O-TETRADECANOYLPHORBOL-13-ACETATE AND THE RAS ONCOGENE MODULATE EXPRESSION AND PHOSPHORYLATION OF GAP JUNCTION PROTEINS [J].
BRISSETTE, JL ;
KUMAR, NM ;
GILULA, NB ;
DOTTO, GP .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (10) :5364-5371
[5]   GAP JUNCTIONAL INTERCELLULAR COMMUNICATION IN MOUSE LUNG EPITHELIAL-CELL LINES - EFFECTS OF CELL-TRANSFORMATION AND TUMOR PROMOTERS [J].
CHAUDHURI, R ;
SIGLER, K ;
DUPONT, E ;
TROSKO, JE ;
MALKINSON, AM ;
RUCH, RJ .
CANCER LETTERS, 1993, 71 (1-3) :11-18
[6]   LIMITING FACTORS OF THE V79 CELL METABOLIC COOPERATION ASSAY FOR TUMOR PROMOTERS [J].
DORMAN, BH ;
BOREIKO, CJ .
CARCINOGENESIS, 1983, 4 (07) :873-877
[7]  
ENOMOTO T, 1985, CANCER RES, V45, P3706
[8]   GAP JUNCTIONAL INTERCELLULAR COMMUNICATION AND CONNEXIN EXPRESSION IN NORMAL AND SV 40-TRANSFORMED HUMAN LIVER-CELLS IN-VITRO [J].
FITZGERALD, DJ ;
SWIERENGA, SHH ;
MESNIL, M ;
PICCOLI, C ;
MARCEAU, N ;
YAMASAKI, H .
CANCER LETTERS, 1993, 71 (1-3) :157-165
[9]  
FITZGERALD DJ, 1990, TERATOGEN CARCIN MUT, V10, P89
[10]   TUMOR PROMOTION RELATED EFFECTS BY THE CYCLODIENE INSECTICIDE ENDOSULFAN STUDIED INVITRO AND INVIVO [J].
FLODSTROM, S ;
WARNGARD, L ;
HEMMING, H ;
FRANSSON, R ;
AHLBORG, UG .
PHARMACOLOGY & TOXICOLOGY, 1988, 62 (04) :230-235