INCREASED EXPRESSION OF INTERCELLULAR-ADHESION MOLECULE-1, CD11 CD18 CELL-SURFACE ADHESION GLYCOPROTEINS AND ALPHA-4-BETA-1 INTEGRIN IN A RAT MODEL OF CHRONIC INTERSTITIAL LUNG FIBROSIS/
N. Barquin et al., INCREASED EXPRESSION OF INTERCELLULAR-ADHESION MOLECULE-1, CD11 CD18 CELL-SURFACE ADHESION GLYCOPROTEINS AND ALPHA-4-BETA-1 INTEGRIN IN A RAT MODEL OF CHRONIC INTERSTITIAL LUNG FIBROSIS/, Pathobiology, 64(4), 1996, pp. 187-192
The expression of the intercellular adhesion molecule 1 (ICAM-1), and
the integrins CD49, CD11b/c, and CD11a(LFA-1 alpha chain) was analyzed
in an experimental model of pulmonary fibrosis. Adult rats were expos
ed to 75% oxygen during 10 weeks, and to 2.0 mg/kg of paraquat twice w
eekly. Rats were sacrificed at 2 days, and at 2 and 10 weeks after the
first injection of paraquat. Lungs were fixed in 4% paraformaldehyde
and used for histology and immunohistochemistry. At 2 days the lungs s
howed a diffuse inflammation composed of a mixed polymorphonuclear and
mononuclear cell infiltrate. Afterwards, the inflammatory process was
predominantly mononuclear, and an increasing fibroblast proliferation
was observed. Early inflammatory events (48 h) correlated with a mode
rate increased expression of ICAM-1, LFA, and CD11b/c in epithelial ce
lls as well as a pronounced expression of ICAM-1 and CD11b/c in macrop
hages. At 2 and 10 weeks, there was a progressive increased expression
of CD11b/c and ICAM-1 by macrophages, as well as of LFA in epithelial
cells, and of ICAM-1 and CD49 by epithelial and interstitial cells. L
ymphocytes showed a slight increased expression of LFA at 2 weeks, and
of CD49 at 2 and 10 weeks. These results suggest that macrophages exp
ressing ICAM-1, CD11b/c, and CD49 are involved in the earlier and late
phases of the disease whereas fibroblast and epithelial cells express
ing ICAM-1 and CD49 might play a role in the cell interactions involve
d in the fibrotic phase.