Modulation of epithelial cell adhesion in gastrointestinal homeostasis

被引:39
作者
Efstathiou, JA
Pignatelli, M
机构
[1] Univ London Imperial Coll Sci Technol & Med, Div Investigat Sci, London W12 0NN, England
[2] John Radcliffe Hosp, Inst Mol Med, Canc Immunogenet Lab, Imperial Canc Res Fund, Oxford OX3 9DS, England
关键词
D O I
10.1016/S0002-9440(10)65576-9
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Cell-cell and cell-matrix interactions are critical to the dynamic processes necessary for tissue morphogenesis in embryos and to the maintenance of complex differentiated tissues in adult organisms. The E- cadherin-catenin and integrin complexes influence and coordinate a variety of cellular processes including adhesion, differentiation, polarity, migration, proliferation, and survival. The suggestion of molecular cross-talk between the cadherin- and integrin-mediated cell adhesion systems, as well as the catenin and EGFR signaling pathways, during the regulation of such cellular processes has important implications for the understanding of gastrointestinal epithelial cell biology. It is therefore not surprising that adhesion-associated molecules are common targets for motogenic and mitogenic factors. The modulation of perturbation of cadherin, catenin, and integrin expression and function play a central role in gastrointestinal epithelial homeostasis and in various pathophysiological situations such as the repair of mucosal injury by epithelial restitution. This implies the potential for the clinical and pharmacological management of chronic ulcerative and inflammatory lesions through the manipulation of cellular adhesive mechanisms. However, to validate such an approach we need appropriate animal models which more closely mimic human gastrointestinal disease. Further development and refinement of such models combined with the elucidation of the biochemical and genetic processes involved will allow investigation into novel treatment, management, and prevention protocols.
引用
收藏
页码:341 / 347
页数:7
相关论文
共 89 条
[1]   EXPERIMENTAL ULCERATION LEADS TO SEQUENTIAL EXPRESSION OF SPASMOLYTIC POLYPEPTIDE, INTESTINAL TREFOIL FACTOR, EPIDERMAL GROWTH-FACTOR AND TRANSFORMING GROWTH-FACTOR-ALPHA MESSENGER-RNAS IN RAT STOMACH [J].
ALISON, MR ;
CHINERY, R ;
POULSOM, R ;
ASHWOOD, P ;
LONGCROFT, JM ;
WRIGHT, NA .
JOURNAL OF PATHOLOGY, 1995, 175 (04) :405-414
[2]   Oral trefoil peptides protect against ethanol- and indomethacin-induced gastric injury in rats [J].
Babyatsky, MW ;
deBeaumont, M ;
Thim, L ;
Podolsky, DK .
GASTROENTEROLOGY, 1996, 110 (02) :489-497
[3]   HUMAN ENTEROCYTE (CACO-2) MIGRATION IS MODULATED INVITRO BY EXTRACELLULAR-MATRIX COMPOSITION AND EPIDERMAL GROWTH-FACTOR [J].
BASSON, MD ;
MODLIN, IM ;
MADRI, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (01) :15-23
[4]   LOSS OF EPITHELIAL DIFFERENTIATION AND GAIN OF INVASIVENESS CORRELATES WITH TYROSINE PHOSPHORYLATION OF THE E-CADHERIN BETA-CATENIN COMPLEX IN CELLS TRANSFORMED WITH A TEMPERATURE-SENSITIVE V-SRC GENE [J].
BEHRENS, J ;
VAKAET, L ;
FRIIS, R ;
WINTERHAGER, E ;
VANROY, F ;
MAREEL, MM ;
BIRCHMEIER, W .
JOURNAL OF CELL BIOLOGY, 1993, 120 (03) :757-766
[5]  
BODMER WF, 1996, SOMATIC EVOLUTION CA, P1
[6]   ADHESION BETWEEN EPITHELIAL-CELLS AND T-LYMPHOCYTES MEDIATED BY E-CADHERIN AND THE ALPHA(E)BETA(7) INTEGRIN [J].
CEPEK, KL ;
SHAW, SK ;
PARKER, CM ;
RUSSELL, GJ ;
MORROW, JS ;
RIMM, DL ;
BRENNER, MB .
NATURE, 1994, 372 (6502) :190-193
[7]   IMMUNOPRECIPITATION AND CHARACTERIZATION OF A BINDING-PROTEIN SPECIFIC FOR THE PEPTIDE, INTESTINAL TREFOIL FACTOR [J].
CHINERY, R ;
COX, HM .
PEPTIDES, 1995, 16 (04) :749-755
[8]   COMBINED INTESTINAL TREFOIL FACTOR AND EPIDERMAL GROWTH-FACTOR IS PROPHYLACTIC AGAINST INDOMETHACIN-INDUCED GASTRIC DAMAGE IN THE RAT [J].
CHINERY, R ;
PLAYFORD, RJ .
CLINICAL SCIENCE, 1995, 88 (04) :401-403
[9]   TREFOIL PEPTIDES PROMOTE EPITHELIAL MIGRATION THROUGH A TRANSFORMING GROWTH-FACTOR BETA-INDEPENDENT PATHWAY [J].
DIGNASS, A ;
LYNCHDEVANEY, K ;
KINDON, H ;
THIM, L ;
PODOLSKY, DK .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (01) :376-383
[10]   OVEREXPRESSION OF ERBB2 IN HUMAN MAMMARY EPITHELIAL-CELLS SIGNALS INHIBITION OF TRANSCRIPTION OF THE E-CADHERIN GENE [J].
DSOUZA, B ;
TAYLORPAPADIMITRIOU, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (15) :7202-7206