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Updated: Aug 2, 2026

Detection of Functional Matrix Metalloproteinases by Zymography
Published on: November 9, 2010
A possible role for metalloproteinases in renal cyst development
N Obermüller1, N Morente, B Kränzlin
1Medical Research Center, Klinikum Mannheim, University of Heidelberg, 68167 Mannheim, Germany.
Matrix metalloproteinase inhibitors show promise for treating polycystic kidney disease. Targeting these enzymes reduced cyst growth and kidney weight in a rat model, suggesting a new therapeutic avenue.
Area of Science:
- Nephrology
- Oncology
- Biochemistry
Background:
- Polycystic kidney disease (PKD) cyst expansion resembles extracellular matrix invasion by tumors.
- Cyst-lining epithelial cells may produce matrix-degrading enzymes.
Purpose of the Study:
- Hypothesize that metalloproteinases are involved in PKD cyst growth.
- Investigate metalloproteinase inhibitors as a therapeutic strategy for PKD.
Main Methods:
- In situ hybridization to analyze gene expression in a (cy/+) rat model of autosomal-dominant PKD.
- Treatment of (cy/+) rats with the metalloproteinase inhibitor batimastat.
Main Results:
- Upregulated matrix metalloproteinase-14 (MMP-14) mRNA found in cyst-lining epithelia and distal tubules.
- Transforming growth factor-beta2 (TGF-beta2) expressed by cyst wall epithelia.
- Batimastat treatment significantly reduced cyst number and kidney weight.
Conclusions:
- Metalloproteinases are implicated in the pathogenesis of PKD.
- Metalloproteinase inhibitors represent a potential therapeutic approach for PKD.
- This strategy may be applicable regardless of the specific PKD background.
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