Trefoil factor family-peptides promote migration of human bronchial epithelial cells - Synergistic effect with epidermal growth factor

Citation
M. Oertel et al., Trefoil factor family-peptides promote migration of human bronchial epithelial cells - Synergistic effect with epidermal growth factor, AM J RESP C, 25(4), 2001, pp. 418-424
Citations number
50
Categorie Soggetti
da verificare
Journal title
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY
ISSN journal
10441549 → ACNP
Volume
25
Issue
4
Year of publication
2001
Pages
418 - 424
Database
ISI
SICI code
1044-1549(200110)25:4<418:TFFPMO>2.0.ZU;2-L
Abstract
A process termed "restitution" enables rapid repair of the respiratory epit helium by migration of neighbouring cells. Mucin-associated TFF-pepticles ( formerly P-domain peptides or trefoil factors) are typical motogens enhanci ng migration of cells in various in vitro models mimicking restitution of t he intestine. The human bronchial epithelial cell line BEAS-2B was used as a model system of airway restitution. The motogenic activities of recombina nt human TFF2 as well as porcine TFF2 were demonstrated by in vitro wound h ealing assays of BEAS-2B cells. TFF2 did not induce phosphorylation of the epidermal growth factor (EGF) receptor. EGF was capable of enhancing the mo togenic effect of human TFF2 at a concentration of 3 X 10(-10) M whereas EG F itself (i.e., in the absence of TFF2) did not stimulate migration at this low concentration. Furthermore, TFF2 as well as monomeric and dimeric form s of TFF3 enhanced migration of BEAS-2B cells in Boyden chambers. Motogenic activity of TFF2 was also shown for normal human bronchial epithelial (NHB E) cells in Boyden chambers. These results suggest that TFF-pepticles act a s motogens in the human respiratory epithelium triggering rapid repair of d amaged mucosa in the course of airway diseases such as asthma.