PHOSPHATIDYLCHOLINE COULD BE THE SOURCE OF 1,2-DAG WHICH ACTIVATES PROTEIN-KINASE-C IN EGF-STIMULATED COLON-CARCINOMA CELLS (HT29)

被引:11
|
作者
BALOGH, A
CSUKA, O
TEPLAN, I
KERI, G
机构
[1] SEMMELWEIS UNIV MED,HUNGARIAN ACAD SCI,SCH MED,INST BIOCHEM 1,H-1444 BUDAPEST,HUNGARY
[2] NATL INST ONCOL,BUDAPEST,HUNGARY
基金
匈牙利科学研究基金会;
关键词
EPIDERMAL GROWTH FACTOR; TYROSINE KINASE ACTIVITY; PROTEIN KINASE C; PHOSPHATIDYLINOSITOLS; PHOSPHATIDYLCHOLINE; 12-O-TETRADECANOYLPHORBOL-1; 3; -ACETATE; COLON CARCINOMA;
D O I
10.1016/0898-6568(95)02007-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In our previous study (A. Balogh et al, Cell. Signalling 5 (6), 795-802, 1993.), we have shown that epidermal growth factor (EGF) increased protein kinase C (PKC) activities in colon carcinoma cell line (HT29), possibly through the increased 1,2-diacylglycerol (1,2-DAG) production via phosphatidylcholine (PC). Here we investigate the effect of the well-known PKC activator 12-O-tetradecanoyl-2 phorbol-13-acetate (TPA), on the levels of P-32 incorporation into EGF induced phosphatidylinositols (PI, PI4P, PI4, 5P(2)) and different phospholipids (PC, PA, PS) as well as on induced tyrosine kinase activity. TPA significantly decreased the effects of EGF and it had the biggest inhibitory effect on EGF induced PC level. These data support our contention that PC plays an important role in the activation of PKC via 1,2-DAG production in the EGF stimulated pathway.
引用
收藏
页码:793 / 801
页数:9
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