The cysteine protease inhibitors cystatins inhibit herpes simplex virus type 1-induced apoptosis and virus yield in HEp-2 cells
(2007) In Journal of General Virology 88(8). p.2101-2105- Abstract
- The role of cystatins in herpes simplex virus (HSV)-induced apoptosis and viral replication has been studied. Human epithelial (HEp-2) cells infected with wild-type HSV-1 (F), with a deletion virus lacking the anti-apoptotic gene Us3 (R7041) or with a deletion virus lacking the anti-apoptotic genes Us3 and ICP4 (d120) were treated with cystatin A, C or D. Cells and culture media were studied at different time points for replicating HSV-1 and for apoptosis. Cystatins C and D inhibited the yield of replicative HSV-1 significantly in HEp-2 cells. In addition, cystatin D inhibited R7041 and d120 virus-induced apoptosis. Moreover, cystatin A inhibited R7041 induced apoptosis. These inhibitory effects of cystatins on virus replication and... (More)
- The role of cystatins in herpes simplex virus (HSV)-induced apoptosis and viral replication has been studied. Human epithelial (HEp-2) cells infected with wild-type HSV-1 (F), with a deletion virus lacking the anti-apoptotic gene Us3 (R7041) or with a deletion virus lacking the anti-apoptotic genes Us3 and ICP4 (d120) were treated with cystatin A, C or D. Cells and culture media were studied at different time points for replicating HSV-1 and for apoptosis. Cystatins C and D inhibited the yield of replicative HSV-1 significantly in HEp-2 cells. In addition, cystatin D inhibited R7041 and d120 virus-induced apoptosis. Moreover, cystatin A inhibited R7041 induced apoptosis. These inhibitory effects of cystatins on virus replication and apoptosis are likely to be separate functions. Cystatin D treatment decreased cellular cathepsin B activity in HSV-1 infection, suggesting that cathepsin B is involved in virus-induced apoptosis. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/688944
- author
- Peri, Piritta ; Hukkanen, Veijo ; Nuutila, Kristiina ; Saukko, Pekka ; Abrahamson, Magnus LU and Vuorinen, Tytti
- organization
- publishing date
- 2007
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Journal of General Virology
- volume
- 88
- issue
- 8
- pages
- 2101 - 2105
- publisher
- Microbiology Society
- external identifiers
-
- wos:000248828600002
- scopus:34547569644
- pmid:17622610
- ISSN
- 1465-2099
- DOI
- 10.1099/vir.0.82990-0
- language
- English
- LU publication?
- yes
- id
- 44fd313f-ce56-4e59-a9e8-c0674b0ea327 (old id 688944)
- date added to LUP
- 2016-04-01 16:10:57
- date last changed
- 2022-01-28 17:55:26
@article{44fd313f-ce56-4e59-a9e8-c0674b0ea327, abstract = {{The role of cystatins in herpes simplex virus (HSV)-induced apoptosis and viral replication has been studied. Human epithelial (HEp-2) cells infected with wild-type HSV-1 (F), with a deletion virus lacking the anti-apoptotic gene Us3 (R7041) or with a deletion virus lacking the anti-apoptotic genes Us3 and ICP4 (d120) were treated with cystatin A, C or D. Cells and culture media were studied at different time points for replicating HSV-1 and for apoptosis. Cystatins C and D inhibited the yield of replicative HSV-1 significantly in HEp-2 cells. In addition, cystatin D inhibited R7041 and d120 virus-induced apoptosis. Moreover, cystatin A inhibited R7041 induced apoptosis. These inhibitory effects of cystatins on virus replication and apoptosis are likely to be separate functions. Cystatin D treatment decreased cellular cathepsin B activity in HSV-1 infection, suggesting that cathepsin B is involved in virus-induced apoptosis.}}, author = {{Peri, Piritta and Hukkanen, Veijo and Nuutila, Kristiina and Saukko, Pekka and Abrahamson, Magnus and Vuorinen, Tytti}}, issn = {{1465-2099}}, language = {{eng}}, number = {{8}}, pages = {{2101--2105}}, publisher = {{Microbiology Society}}, series = {{Journal of General Virology}}, title = {{The cysteine protease inhibitors cystatins inhibit herpes simplex virus type 1-induced apoptosis and virus yield in HEp-2 cells}}, url = {{http://dx.doi.org/10.1099/vir.0.82990-0}}, doi = {{10.1099/vir.0.82990-0}}, volume = {{88}}, year = {{2007}}, }