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Glycosaminoglycans Modify Elastase ActionIn Vitroand Enhance Elastase-Induced Cell Death in Cultured Fibroblasts
Author(s) -
José Oliveira dos Santos,
Viviane Abreu Nunes,
Ilana Cruz-Silva,
Priscila Praxedes-Garcia,
Andrezza Justino Gozzo,
Mariana Rydlewski,
Yamilé González,
Helena B. Nader,
Mariana S. Araújo
Publication year - 2011
Publication title -
isrn cell biology
Language(s) - English
Resource type - Journals
eISSN - 2090-7389
pISSN - 2090-7370
DOI - 10.5402/2012/973983
Subject(s) - glycosaminoglycan , heparan sulfate , extracellular matrix , elastase , chondroitin sulfate , fibroblast , microbiology and biotechnology , dermatan sulfate , chemistry , pancreatic elastase , apoptosis , dna fragmentation , cell , viability assay , in vitro , cell culture , biochemistry , enzyme , programmed cell death , biology , genetics
Human neutrophil elastase (HNE) has been shown to be involved on death of different cell types, including epithelial lung cells, which is related to several pulmonary diseases. Since HNE activity may be influenced by extracellular matrix (ECM) molecules such as glycosaminoglycans (GAGs), and fibroblasts are the most common ECM-producing cells of lung connective tissue, the aim of this work was to verify if HNE can induce fibroblast death and to study the enzyme modulation by GAGs. HNE-like activity was mimicked by using human neutrophils conditioned medium (NCM). Heparan sulfate and chondroitin 6-sulfate reduce the enzyme activity and modify its secondary structure. NCM reduced cell viability, and this effect was higher in the presence of those GAGs. NCM also increased DNA fragmentation, suggesting the occurrence of apoptosis, but without influence of GAGs. These results can contribute to the understanding of HNE modulation in physio- and pathological processes where this enzyme is involved.

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