Changes in collagenases and TGF-β; precede structural alterations in a model of chronic renal fibrosis

Autor: Wa Mo, Alfredo A. Pegoraro, Julienne Au, Sandra L. Garber, Jose A.L. Arruda, Ashok Kumar Singh, Carolyn Brecklin, Ruo H. Song, George Dunea
Jazyk: angličtina
Předmět:
Zdroj: Kidney International. (1):145-153
ISSN: 0085-2538
DOI: 10.1046/j.1523-1755.1999.00545.x
Popis: Changes in collagenases and TGF-βbgr; precede structural alterations in a model of chronic renal fibrosis. Background To study the role of collagenases and transforming growth factor-βbgr; (TGF-βbgr;) in the genesis of interstitial fibrosis, we used the model of bromoethylamine (BEA)-induced papillary necrosis, which is known to lead over a period of 1 to 12 months to interstitial fibrosis and renal insufficiency. Methods Rats were injected with BEA, and urine and kidney tissue (cortex and medulla) were collected after 1, 2, 3, 7, and 30 days. One kidney was perfused and fixed for morphological studies and immunostained for collagen type I, III, and IV. The other kidney was used to prepare cortex and medulla extracts for gelatinases (by fluorometric and zymographic techniques), tissue inhibitors of metalloproteinase-1 (TIMP-1), and TIMP-2 (by enzyme-linked immunosorbent assay, ELISA) and TGF-βbgr;1 (by ELISA). Results Albuminuria and interstitial fibrosis were present in BEA rats by day 7, which continued until day 30. Immunocytochemical staining for collagen types showed that collagen III and IV increased in the interstitium by day 30, but collagen I remained unchanged. Gelatinase activity in the medulla decreased by 57% compared with control by day 2 and remained low until day 30. In the cortex, gelatinase activity remained unchanged between 0 and 7 days after BEA but decreased by 72% by day 30. TIMP-1 and TIMP-2 were decreased by 80% compared with day 0 in both the medulla (by day 1) and cortex (by day 2) and remained low up to day 30. TGF-βbgr;1 immunoreactivity increased progressively until day 2 in the medulla (16-fold higher than control) and day 3 in the cortex (8-fold higher than control) and returned to control level by day 3 in the medulla and by day 30 in the cortex. Two days after BEA injection, the mRNA for TGF-βbgr;1 was increased eightfold in the cortex and 12-fold in the medulla, and it remained high for up to 30 days. Conclusions The fibrosis that follows papillary necrosis is associated with both high TGF-βbgr;1 expression and depressed gelatinolytic activity.
Databáze: OpenAIRE