Ca. Herbert et al., STIMULATED EOSINOPHILS AND PROTEINASES AUGMENT THE TRANSEPITHELIAL FLUX OF ALBUMIN IN BOVINE BRONCHIAL-MUCOSA, British Journal of Pharmacology, 110(2), 1993, pp. 840-846
1 The apical to basolateral transmucosal flux of albumin has been meas
ured in isolated sheets of bovine bronchial and tracheal mucosa. Under
resting conditions the net unidirectional flux in the bronchial mucos
a was not significantly different from that measured previously for th
e basolateral to apical vector. In contrast, the apical to basolateral
flux in the tracheal mucosa was significantly lower than that measure
d in the opposite direction. 2 Addition of guinea-pig peritoneal eosin
ophils to the apical side of the tissues had no significant effect on
the transmucosal flux of albumin in either the bronchial or tracheal m
ucosa. 3 When eosinophils were stimulated with the ionophore A23187 or
by opsonic adherence to tissues treated with a guinea-pig anti-bovine
airway epithelium antibody, the bronchial mucosal sheets that had bee
n exposed showed a significant increase in the transmucosal flux of al
bumin. However, tissues from the tracheal mucosa were resistant to the
effects of stimulated eosinophils. 4 Histologically, sheets of mucosa
from bovine main bronchi that had been exposed to stimulated eosinoph
ils were characterized by epithelial injury consisting of loss of colu
mnar epithelium from the underlying basal cell layer and biomatrix. Mu
ch less evidence of cellular injury was observed in tracheal tissues.
5 Bacterial collagenases applied to the apical side of the sheets were
shown to increase the permeability of the bronchial mucosa to albumin
and to produce histological changes that had similarities with the pa
ttern of damage produced by stimulated eosinophils. 6 These observatio
ns demonstrate that the ability of eosinophils to injure the bronchial
mucosa is independent of the side of the tissue on which they are pre
sent. Furthermore, key aspects of the injury process may be reproduced
, at least in part, by metalloproteinases.