Skin wound healing exhibits type III collagen synthesis occurring transient
ly as early as 10 h after injury, with subsequent synthesis of type I to fo
rm a scar. We hypothesized that similar collagen type switching also occurr
ed in the bleomycin model of lung fibrosis in the rat. We could measure ele
vated lung collagen synthesis rates as early as 4 days after administration
of bleomycin. Collagen type I:III ratios in whole lung remained constant f
or the first 7 days at the control level of 2:1, then increased to as high
as 5:1 at day 21. Procollagen mRNA content, expressed as a ratio of type I:
III mRNAs, was consistent with the protein synthesis data and the observed
ratio of collagen types bring made by the lungs at the various time points
evaluated. We conclude that a transient increase in type III relative to ty
pe I collagen does not occur in the bleomycin rat lung model. Therefore, th
e sequence of type-specific collagen expression and deposition in the skin
wound healing model is not entirely analogous to this widely used animal mo
del of pulmonary fibrosis. (C) 2000 Elsevier Science Ireland Ltd. All right
s reserved.