In vitro hypoxia increases production of matrix metalloproteinases and tryptase in isolated rat lung mast cells
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
18052689
DOI
10.33549/physiolres.931278
PII: 1278
Knihovny.cz E-zdroje
- MeSH
- hypoxie buňky MeSH
- imunohistochemie MeSH
- kolagen metabolismus MeSH
- krysa rodu Rattus MeSH
- kultivační média metabolismus MeSH
- kultivované buňky MeSH
- mastocyty enzymologie MeSH
- matrixová metaloproteinasa 13 metabolismus MeSH
- matrixová metaloproteinasa 2 metabolismus MeSH
- matrixová metaloproteinasa 9 metabolismus MeSH
- matrixové metaloproteinasy metabolismus MeSH
- plíce cytologie enzymologie MeSH
- potkani Wistar MeSH
- separace buněk MeSH
- tryptasy metabolismus MeSH
- upregulace MeSH
- western blotting MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- kolagen MeSH
- kultivační média MeSH
- matrixová metaloproteinasa 13 MeSH
- matrixová metaloproteinasa 2 MeSH
- matrixová metaloproteinasa 9 MeSH
- matrixové metaloproteinasy MeSH
- Mmp13 protein, rat MeSH Prohlížeč
- Mmp2 protein, rat MeSH Prohlížeč
- Mmp9 protein, mouse MeSH Prohlížeč
- tryptasy 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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