LOCALIZATION OF TRANSFORMING GROWTH-FACTOR-BETA ISOFORMS TGF-BETA-1, TGF-BETA-2, AND TGF-BETA-3 IN SURGICALLY INDUCED PELVIC ADHESIONS IN THE RAT

Objective: To investigate the presence and cellular distribution of tr ansforming growth factor (TGF)-beta s in surgically induced pelvic fib rous adhesions in rat uterine horns subjected to burn, crush, and debr idement injury. Methods: Thirty injured and 20 uninjured rats were tre ated postoperatively with intraperitoneal administration of either 2 m u g/mL of recombinant human TGF-beta, 10 mu g/mL TGF-beta neutralizing antibody, or phosphate-buffered saline + 500 mu g rat serum albumin f or 5 consecutive days. The intact (uninjured) and fibrous tissues were analyzed immunohistochemically for the presence of TGF-beta s using p olyclonal antibodies to TGF-beta s 1-3. Results: The intact peritoneum immunostained with a lower intensity than fibrous adhesive tissues fo r TGF-beta 1, TGF-beta 2, and TGF-beta 3. The immunoreactive TGF-beta s were present in fibroblasts, inflammatory cells infiltrated into the fibrous adhesion, and endothelial and smooth-muscle cells of the arte rioles. In the uterine tissue at the site of injury, the following imm unostained for TGF-beta s: uterine serosal tissue, myometrial smooth-m uscle cells, endometrial luminal and glandular epithelial cells, and i nflammatory cells. However, endometrial stromal cells did not immunost ain for TGF-beta s. There were no substantial differences in immuno-st aining intensities of fibrous adhesive tissues in the TGF-beta group, neutralizing TGF-beta antibody group, and the controls. Conclusion: Th e data suggest that TGF-beta s may play a role in the formation and ma intenance of fibrous adhesions following intraperitoneal injury.