MAP kinase pathway signalling is essential for extracellular matrix determined mammary epithelial cell survival

被引:40
作者
Finlay, D
Healy, V
Furlong, F
O'Connell, FC
Keon, NK
Martin, F [1 ]
机构
[1] Univ Coll Dublin, Conway Inst Biomol & Biomed Res, Dept Pharmacol, Dublin 4, Ireland
[2] Univ Coll Dublin, Ctr Biotechnol, Dublin 4, Ireland
关键词
Erk; apoptosis; p38; MAPK; epithelial; PD; 98059; SB; 203580; ECM;
D O I
10.1038/sj.cdd.4400652
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
Mammary epithelial cells in primary cell culture require both growth factors and specific extracellular matrix (ECM)attachment for survival. Here we demonstrate for the first time that inhibition of the ECM-induced Erk 1/Erk 2 (p42/44 MAPK) pathway, by PD 98059, leads to apoptosis in these cells. Associated with this cell death is a possible compensatory signalling through the p38 MAP kinase pathway the inhibition of which, by SE 203580, leads to a more rapid onset of apoptosis. This provides evidence for a hitherto undescribed Erk 1/Erk 2 to p38 MAP kinase pathway 'cross-talk' that is essential for the survival of these cells. The cell death associated with inhibition of these two MAP kinase pathways however, occurred in the presence of insulin that activates the, classical PI-3 kinase-dependent Akt/PKB survival signals and Akt phosphorylation. Cell death induced by inhibition of the MAP kinase pathways did not affect Akt phosphorylation and may, thus, be independent of PI-3 kinase signalling.
引用
收藏
页码:302 / 313
页数:12
相关论文
共 74 条
[1]   Differential effect of components of the extracellular matrix on differentiation and apoptosis [J].
Aharoni, D ;
Meiri, I ;
Atzmon, R ;
Vlodavsky, I ;
Amsterdam, A .
CURRENT BIOLOGY, 1997, 7 (01) :43-51
[2]   PD-098059 IS A SPECIFIC INHIBITOR OF THE ACTIVATION OF MITOGEN-ACTIVATED PROTEIN-KINASE KINASE IN-VITRO AND IN-VIVO [J].
ALESSI, DR ;
CUENDA, A ;
COHEN, P ;
DUDLEY, DT ;
SALTIEL, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (46) :27489-27494
[3]  
BARCELLOSHOFF MH, 1989, DEVELOPMENT, V105, P223
[4]   The activation of p38 and apoptosis by the inhibition of ERK is antagonized by the phosphoinositide S-kinase/Akt pathway [J].
Berra, E ;
Diaz-Meco, MT ;
Moscat, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (17) :10792-10797
[5]   Extracellular matrix and integrin signalling: the shape of things to come [J].
Boudreau, J ;
Jones, PL .
BIOCHEMICAL JOURNAL, 1999, 339 :481-488
[6]   SUPPRESSION OF ICE AND APOPTOSIS IN MAMMARY EPITHELIAL-CELLS BY EXTRACELLULAR-MATRIX [J].
BOUDREAU, N ;
SYMPSON, CJ ;
WERB, Z ;
BISSELL, MJ .
SCIENCE, 1995, 267 (5199) :891-893
[7]   Suppression of apoptosis by basement membrane requires three-dimensional tissue organization and withdrawal from the cell cycle [J].
Boudreau, N ;
Werb, Z ;
Bissell, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) :3509-3513
[8]   Ras activation is necessary for integrin-mediated activation of extracellular signal-regulated kinase 2 and cytosolic phospholipase A(2) but not for cytoskeletal organization [J].
Clark, EA ;
Hynes, RO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (25) :14814-14818
[9]   SB-203580 IS A SPECIFIC INHIBITOR OF A MAP KINASE HOMOLOG WHICH IS STIMULATED BY CELLULAR STRESSES AND INTERLEUKIN-1 [J].
CUENDA, A ;
ROUSE, J ;
DOZA, YN ;
MEIER, R ;
COHEN, P ;
GALLAGHER, TF ;
YOUNG, PR ;
LEE, JC .
FEBS LETTERS, 1995, 364 (02) :229-233
[10]   Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery [J].
Datta, SR ;
Dudek, H ;
Tao, X ;
Masters, S ;
Fu, HA ;
Gotoh, Y ;
Greenberg, ME .
CELL, 1997, 91 (02) :231-241