Cargando…
An earthworm protease cleaving serum fibronectin and decreasing HBeAg in HepG2.2.15 cells
BACKGROUND: Virus-binding activity is one of the important functions of fibronectin (FN). It has been reported that a high concentration of FN in blood improves the transmission frequency of hepatitis viruses. Therefore, to investigate a protease that hydrolyzes FN rapidly is useful to decrease the...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2611985/ https://www.ncbi.nlm.nih.gov/pubmed/19025649 http://dx.doi.org/10.1186/1471-2091-9-30 |
_version_ | 1782163108550148096 |
---|---|
author | Wang, Xue-Qing Chen, Lan Pan, Rong Zhao, Jing Liu, Ying He, Rong-Qiao |
author_facet | Wang, Xue-Qing Chen, Lan Pan, Rong Zhao, Jing Liu, Ying He, Rong-Qiao |
author_sort | Wang, Xue-Qing |
collection | PubMed |
description | BACKGROUND: Virus-binding activity is one of the important functions of fibronectin (FN). It has been reported that a high concentration of FN in blood improves the transmission frequency of hepatitis viruses. Therefore, to investigate a protease that hydrolyzes FN rapidly is useful to decrease the FN concentration in blood and HBV infection. So far, however, no specific protease digesting FN in serum has been reported. METHODS: We employed a purified earthworm protease to digest serum proteins. The rapidly cleaved protein (FN) was identified by MALDI-TOF MS and western blotting. The cleavage sites were determined by N-terminus amino acid residues sequencing. The protease was orally administrated to rats to investigate whether serum FN in vivo became decreased. The serum FN was determined by western blotting and ELISA. In cytological studies, the protease was added to the medium in the culture of HepG2.2.15 cells and then HBsAg and HBeAg were determined by ELISA. RESULTS: The protease purified from earthworm Eisenia fetida was found to function as a fibronectinase (FNase). The cleavage sites on FN by the FNase were at R and K, exhibiting a trypsin alkaline serine-like function. The earthworm fibronectinase (EFNase) cleaved FN at four sites, R(259), R(1005), K(1557 )and R(2039), among which the digested fragments at R(259), K(1557 )and R(2039 )were related to the virus-binding activity as reported. The serum FN was significantly decreased when the earthworm fibronectinase was orally administrated to rats. The ELISA results showed that the secretion of HBeAg from HepG2.2.15 cells was significantly inhibited in the presence of the FNase. CONCLUSION: The earthworm fibronectinase (EFNase) cleaves FN much faster than the other proteins in serum, showing a potential to inhibit HBV infection through its suppressing the level of HBeAg. This suggests that EFNase is probably used as one of the candidates for the therapeutic agents to treat hepatitis virus infection. |
format | Text |
id | pubmed-2611985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26119852008-12-30 An earthworm protease cleaving serum fibronectin and decreasing HBeAg in HepG2.2.15 cells Wang, Xue-Qing Chen, Lan Pan, Rong Zhao, Jing Liu, Ying He, Rong-Qiao BMC Biochem Research Article BACKGROUND: Virus-binding activity is one of the important functions of fibronectin (FN). It has been reported that a high concentration of FN in blood improves the transmission frequency of hepatitis viruses. Therefore, to investigate a protease that hydrolyzes FN rapidly is useful to decrease the FN concentration in blood and HBV infection. So far, however, no specific protease digesting FN in serum has been reported. METHODS: We employed a purified earthworm protease to digest serum proteins. The rapidly cleaved protein (FN) was identified by MALDI-TOF MS and western blotting. The cleavage sites were determined by N-terminus amino acid residues sequencing. The protease was orally administrated to rats to investigate whether serum FN in vivo became decreased. The serum FN was determined by western blotting and ELISA. In cytological studies, the protease was added to the medium in the culture of HepG2.2.15 cells and then HBsAg and HBeAg were determined by ELISA. RESULTS: The protease purified from earthworm Eisenia fetida was found to function as a fibronectinase (FNase). The cleavage sites on FN by the FNase were at R and K, exhibiting a trypsin alkaline serine-like function. The earthworm fibronectinase (EFNase) cleaved FN at four sites, R(259), R(1005), K(1557 )and R(2039), among which the digested fragments at R(259), K(1557 )and R(2039 )were related to the virus-binding activity as reported. The serum FN was significantly decreased when the earthworm fibronectinase was orally administrated to rats. The ELISA results showed that the secretion of HBeAg from HepG2.2.15 cells was significantly inhibited in the presence of the FNase. CONCLUSION: The earthworm fibronectinase (EFNase) cleaves FN much faster than the other proteins in serum, showing a potential to inhibit HBV infection through its suppressing the level of HBeAg. This suggests that EFNase is probably used as one of the candidates for the therapeutic agents to treat hepatitis virus infection. BioMed Central 2008-11-24 /pmc/articles/PMC2611985/ /pubmed/19025649 http://dx.doi.org/10.1186/1471-2091-9-30 Text en Copyright © 2008 Wang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wang, Xue-Qing Chen, Lan Pan, Rong Zhao, Jing Liu, Ying He, Rong-Qiao An earthworm protease cleaving serum fibronectin and decreasing HBeAg in HepG2.2.15 cells |
title | An earthworm protease cleaving serum fibronectin and decreasing HBeAg in HepG2.2.15 cells |
title_full | An earthworm protease cleaving serum fibronectin and decreasing HBeAg in HepG2.2.15 cells |
title_fullStr | An earthworm protease cleaving serum fibronectin and decreasing HBeAg in HepG2.2.15 cells |
title_full_unstemmed | An earthworm protease cleaving serum fibronectin and decreasing HBeAg in HepG2.2.15 cells |
title_short | An earthworm protease cleaving serum fibronectin and decreasing HBeAg in HepG2.2.15 cells |
title_sort | earthworm protease cleaving serum fibronectin and decreasing hbeag in hepg2.2.15 cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2611985/ https://www.ncbi.nlm.nih.gov/pubmed/19025649 http://dx.doi.org/10.1186/1471-2091-9-30 |
work_keys_str_mv | AT wangxueqing anearthwormproteasecleavingserumfibronectinanddecreasinghbeaginhepg2215cells AT chenlan anearthwormproteasecleavingserumfibronectinanddecreasinghbeaginhepg2215cells AT panrong anearthwormproteasecleavingserumfibronectinanddecreasinghbeaginhepg2215cells AT zhaojing anearthwormproteasecleavingserumfibronectinanddecreasinghbeaginhepg2215cells AT liuying anearthwormproteasecleavingserumfibronectinanddecreasinghbeaginhepg2215cells AT herongqiao anearthwormproteasecleavingserumfibronectinanddecreasinghbeaginhepg2215cells AT wangxueqing earthwormproteasecleavingserumfibronectinanddecreasinghbeaginhepg2215cells AT chenlan earthwormproteasecleavingserumfibronectinanddecreasinghbeaginhepg2215cells AT panrong earthwormproteasecleavingserumfibronectinanddecreasinghbeaginhepg2215cells AT zhaojing earthwormproteasecleavingserumfibronectinanddecreasinghbeaginhepg2215cells AT liuying earthwormproteasecleavingserumfibronectinanddecreasinghbeaginhepg2215cells AT herongqiao earthwormproteasecleavingserumfibronectinanddecreasinghbeaginhepg2215cells |