Induction of in vitro angiogenesis in the endothelial-derived cell line, EA hy926, by ethanol is mediated through PKC and MAPK

被引:52
作者
Jones, MK [1 ]
Sarfeh, IJ
Tarnawski, AS
机构
[1] Dept Vet Affairs Med Ctr, Dept Med, Long Beach, CA 90822 USA
[2] Dept Vet Affairs Med Ctr, Dept Surg, Long Beach, CA 90822 USA
[3] Univ Calif Irvine, Irvine, CA 92717 USA
关键词
protein kinase C; mitogen activated protein; kinase; ERK; MEK; signaling; kinase inhibitors; kinase activation;
D O I
10.1006/bbrc.1998.9095
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have previously shown that ethanol-induced injury to the gastric mucosa triggers increased expression of the angiogenic factors, basic fibroblast growth factor (bFGF) and vascular endothelial growth factor (VEGF) and angiogenesis. To further investigate ethanol-induced angiogenesis, we used an in vitro angiogenesis model which employs the ability of an endothelial-derived cell line (EA hy926) to form tubelike structures resembling capillaries when plated on the matrix material, Matrigel. We report that serum-starved EA hy926 cells, incubated for as little as 5 minutes with ethanol concentrations of 1.0-2.5%, formed tubelike structures reflecting in vitro angiogenesis. Control cells, not incubated with ethanol, did not form tubelike structures. incubation for 5 minutes with 2.5% ethanol resulted in increased activities of PKC and MAP kinase (ERK2) by 1.6-fold (p < 0.05) and 2.3-fold (P < 0.001), respectively. Futhermore, inhibitors of the MAPK kinase, MEK (PD98059) and PRC (GF 109203X) prevented the induction of in vitro angiogenesis by ethanol, (C) 1998 Academic Press.
引用
收藏
页码:118 / 123
页数:6
相关论文
共 38 条
[11]   PLASMINOGEN-ACTIVATOR AND COLLAGENASE PRODUCTION BY CULTURED CAPILLARY ENDOTHELIAL-CELLS [J].
GROSS, JL ;
MOSCATELLI, D ;
JAFFE, EA ;
RIFKIN, DB .
JOURNAL OF CELL BIOLOGY, 1982, 95 (03) :974-981
[12]  
HIGASHI K, 1991, J BIOL CHEM, V266, P2178
[13]   DISTORTED MICROANGIOARCHITECTURE AND IMPAIRED ANGIOGENESIS IN GASTRIC-MUCOSA OF PORTAL HYPERTENSIVE RATS [J].
ICHIKAWA, Y ;
TARNAWSKI, A ;
SARFEH, IJ ;
ISHIKAWA, T ;
SHIMADA, H .
GASTROENTEROLOGY, 1994, 106 (03) :702-708
[14]  
Johnson ME, 1996, REGION ANESTH, V21, P6
[15]  
Jones MP, 1998, GASTROENTEROLOGY, V114, pA163, DOI 10.1016/S0016-5085(98)80659-8
[16]   PROTEIN KINASE-C MEDIATES PLATELET-DERIVED GROWTH-FACTOR INDUCED TYROSINE PHOSPHORYLATION OF P42 [J].
KAZLAUSKAS, A ;
COOPER, JA .
JOURNAL OF CELL BIOLOGY, 1988, 106 (04) :1395-1402
[17]   REQUIREMENT FOR PROTEIN-KINASE-C ACTIVATION IN BASIC FIBROBLAST GROWTH FACTOR-INDUCED HUMAN ENDOTHELIAL-CELL PROLIFERATION [J].
KENT, KC ;
MII, S ;
HARRINGTON, EO ;
CHANG, JD ;
MALLETTE, S ;
WARE, JA .
CIRCULATION RESEARCH, 1995, 77 (02) :231-238
[18]   INDUCTION OF THE C-JUN PROTOONCOGENE BY A PROTEIN KINASE-C-DEPENDENT MECHANISM DURING EXPOSURE OF HUMAN EPIDERMAL-KERATINOCYTES TO ETHANOL [J].
KHARBANDA, S ;
NAKAMURA, T ;
KUFE, D .
BIOCHEMICAL PHARMACOLOGY, 1993, 45 (03) :675-681
[19]   Cyclin D1 expression is regulated positively by the p42/p44(MAPK) and negatively by the p38/HOG(MAPK) pathway [J].
Lavoie, JN ;
LAllemain, G ;
Brunet, A ;
Muller, R ;
Pouyssegur, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (34) :20608-20616
[20]   Human umbilical vein and dermal microvascular endothelial cells show heterogeneity in response to PKC activation [J].
Mason, JC ;
Yarwood, H ;
Sugars, K ;
Haskard, DO .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1997, 273 (04) :C1233-C1240