In vitro hypoxia increases production of matrix metalloproteinases and tryptase in isolated rat lung mast cells
Language English Country Czech Republic Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18052689
DOI
10.33549/physiolres.931278
PII: 1278
Knihovny.cz E-resources
- MeSH
- Cell Hypoxia MeSH
- Immunohistochemistry MeSH
- Collagen metabolism MeSH
- Rats MeSH
- Culture Media metabolism MeSH
- Cells, Cultured MeSH
- Mast Cells enzymology MeSH
- Matrix Metalloproteinase 13 metabolism MeSH
- Matrix Metalloproteinase 2 metabolism MeSH
- Matrix Metalloproteinase 9 metabolism MeSH
- Matrix Metalloproteinases metabolism MeSH
- Lung cytology enzymology MeSH
- Rats, Wistar MeSH
- Cell Separation MeSH
- Tryptases metabolism MeSH
- Up-Regulation MeSH
- Blotting, Western MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Collagen MeSH
- Culture Media MeSH
- Matrix Metalloproteinase 13 MeSH
- Matrix Metalloproteinase 2 MeSH
- Matrix Metalloproteinase 9 MeSH
- Matrix Metalloproteinases MeSH
- Mmp13 protein, rat MeSH Browser
- Mmp2 protein, rat MeSH Browser
- Mmp9 protein, mouse MeSH Browser
- Tryptases MeSH
Chronic hypoxia results in hypoxic pulmonary hypertension characterized by fibrotization and muscularization of the walls of peripheral pulmonary arteries. This vessel remodeling is accompanied by an increase in the amount of lung mast cells (LMC) and the presence of small collagen cleavage products in the vessel walls. We hypothesize that hypoxia activates LMC, which release matrix metalloproteinases (MMPs) cleaving collagen and starting increased turnover of connective tissue proteins. This study was designed to determine whether in vitro hypoxia stimulates production of MMPs in rat LMC and increases their collagenolytic activity. The LMC were separated on the Percoll gradient and then were divided into two groups and cultivated for 24 h in 21 % O(2) + 5 % CO(2) or in 10 % O(2) + 5 % CO(2). Presence of the rat interstitial tissue collagenase (MMP-13) in LMC was visualized by immunohistological staining and confirmed by Western blot analysis. Total MMPs activity and tryptase activity were measured in both cultivation media and cellular extracts. Exposure to hypoxia in vitro increased the amount of cells positively labeled by anti-MMP-13 antibody as well as activities of all measured enzymes. The results therefore support the concept that LMC are an important source of increased collagenolytic activity in chronic hypoxia.
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