Low-dose exposure of intestinal epithelial cells to formaldehyde results in MAP kinase activation and molecular alteration of the focal adhesion protein paxillin

被引:8
作者
Feick, P [1 ]
Haas, SRL [1 ]
Singer, MV [1 ]
Böcker, U [1 ]
机构
[1] Heidelberg Univ, Dept Med Gastroenterol Hepatol Infect Dis 2, Ctr Environm Med, Med Fac Mannheim, D-68167 Mannheim, Germany
关键词
formaldehyde; intestinal epithelial cell; paxillin; MAP kinase;
D O I
10.1016/j.tox.2005.11.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We investigated the potential pathophysiological role of non-lethal formaldehyde concentrations on human intestinal epithelial HT-29 cells. Expression levels of actin, tubulin and detectable cytokeratin isoforms 5, 13, 18, 19 and 20 were not affected after 24 h of exposure to 1 mM formaldehyde. By contrast, cellular organization of cytoskeletal constituents was already changed after 60 min. Within 15 min, formaldehyde induced profound tyrosine phosphorylation of the focal adhesion protein paxillin and of proteins at about 120-130 kDa. Concomitantly, phosphorylation of ERK-1/2 and p38 MAP kinase occurred. Paxillin was not only tyrosine phosphorylated but underwent a sustained molecular weight shift representing serine/threonine phosphorylation that was independent of MAP kinase activity and EGF-R-mediated signalling. Our data show that exposure of intestinal epithelial cells to low-dose formaldehyde is followed by rapid and profound signalling events. The data suggest a modifier role of environmental or endogenous formaldehyde for epithelial cell functions. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:60 / 72
页数:13
相关论文
共 45 条
[1]   Transforming growth factor-β mediates intestinal healing and susceptibility to injury in vitro and in vivo through epithelial cells [J].
Beck, PL ;
Rosenberg, IM ;
Xavier, RJ ;
Koh, T ;
Wong, JF ;
Podolsky, DK .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 162 (02) :597-608
[2]   Adhesion of fibroblasts to fibronectin stimulates both serine and tyrosine phosphorylation of paxillin [J].
Bellis, SL ;
Perrotta, JA ;
Curtis, MS ;
Turner, CE .
BIOCHEMICAL JOURNAL, 1997, 325 :375-381
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   Serine and threonine phosphorylation of the paxillin LIM domains regulates paxillin focal adhesion localization and cell adhesion to fibronectin [J].
Brown, MC ;
Perrotta, JA ;
Turner, CE .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (07) :1803-1816
[5]   Design, synthesis, and biological evaluation of doxorubicin - Formaldehyde conjugates targeted to breast cancer cells [J].
Burke, PJ ;
Koch, TH .
JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (05) :1193-1206
[6]   TYROSINE PHOSPHORYLATION OF PAXILLIN AND PP125(FAK) ACCOMPANIES CELL-ADHESION TO EXTRACELLULAR-MATRIX - A ROLE IN CYTOSKELETAL ASSEMBLY [J].
BURRIDGE, K ;
TURNER, CE ;
ROMER, LH .
JOURNAL OF CELL BIOLOGY, 1992, 119 (04) :893-903
[7]  
Chautems R C, 2003, Colorectal Dis, V5, P24, DOI 10.1046/j.1463-1318.2003.00396.x
[8]   Prospective evaluation of formalin therapy for radiation proctitis [J].
Counter, SF ;
Froese, DP ;
Hart, MJ .
AMERICAN JOURNAL OF SURGERY, 1999, 177 (05) :396-398
[9]  
Cutts SM, 2001, CANCER RES, V61, P8194
[10]   Formalin application in the treatment of chronic radiation-induced hemorrhagic proctitis - An effective but not risk-free procedure: A prospective study of 33 patients [J].
de Parades, V ;
Etienney, I ;
Bauer, P ;
Bourguignon, J ;
Meary, N ;
Mory, B ;
Sultan, S ;
Taouk, M ;
Thomas, C ;
Atienza, P .
DISEASES OF THE COLON & RECTUM, 2005, 48 (08) :1535-1541