TGF-β2 activates proliferative scar fibroblasts

Background. Cytokines, such as the transforming growth factor beta (TGF-beta) isoforms, have been linked to the formation of proliferative scars. This study examines the stimulating effects of exogenous TGF-beta(2) on cultured keloid, burn hypertrophic scar, and normal skin fibroblasts and whether such effects can be suppressed with TGF-beta(2) antibody. Methods. In vitro, the fibroblast-populated collagen lattice (FPCL) is used in the evaluation of fibroblast activation by measuring contraction of the lattice over time. Primary cultures of fibroblasts were grown from keloids, burn hypertrophic scars, and normal skin using standard cell culture techniques. TGF-beta(2) (10 ng/ml) was added to each of the three types of cell cultures and placed on prefabricated FPCLs. Each was tested against their normal control counterparts. TGF-beta(2) antibody (100 ng/ml) was then placed on the TGF-beta(2)-treated FPCLs. All lattices were allowed to contract and areas were measured for 5 days. Results. Compared to controls, keloid fibroblasts were most affected by the addition of exogenous TGF-beta(2). Normal skin fibroblasts did not show a significant increase in contraction early on, yet a significant difference was seen as time progressed. The addition of TGF-beta(2) antibody inhibited the function of keloid and burn hypertrophic scar fibroblasts. It also reversed the increased contraction of the TFG-beta(2)-treated proliferative scar fibroblasts. Conclusion. By utilizing an in vitro model, we have demonstrated that TGF-beta(2) antibody reverses the increased contraction of FPCLs by proliferative scar fibroblasts treated with TGF-beta(2). This points to a possible treatment modality in patients afflicted with this disfiguring problem. (C) 1999 Academic Press.