The role of microvesicles in cancer and viral infection
Microvesicles are shed constitutively, or upon activation from both normal and malignant cells. Although recent studies have reported various nonlytic virus release mechanisms, this mode of virus transmission to secondary sites of infection has remained unclear. This study identified that Coxsackie...
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| Format: | Thesis |
| Language: | English |
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2012
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| Online Access: | https://repository.londonmet.ac.uk/7489/1/590129.pdf |
| _version_ | 1804072774542557184 |
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| author | Jorfi, Samireh |
| author_facet | Jorfi, Samireh |
| author_sort | Jorfi, Samireh |
| collection | LMU |
| description | Microvesicles are shed constitutively, or upon activation from both normal and malignant cells. Although recent studies have reported various nonlytic virus release mechanisms, this mode of virus transmission to secondary sites of infection has remained unclear. This study identified that Coxsackie virus B1 (CVB1) entry into HeLa cells results in apoptosis and production of virus-induced apoptotic microvesicles (vaMVs) by infected cells. Flow cytometery and fluorescence microscopy data illustrated that these vaMVs carry and disseminate CVB1 virions to new host cells via a non lytic MV-to-cell viral mechanism. Inhibition of MV production by siRNA knockdown of CAPNS1 in HeLa cells suggested that these vesicles mediate the spread of apoptosis to secondary sites of infection and the vaMVs could mediate non lytic MV-to-cell transmission. This thesis also identified a new mechanism for multi-drug resistance involving the efflux of anticancer drugs from cancer cells mediated by release of microvesicles, removing the drug from treated cancer cells. Immunoblotting and flow cytometery data showed that transcriptional silencing of calpain by siRNA knockdown of CAPNS1 in PC3M cells prior to drug treatment inhibits MV release and results in induced apoptosis in cells. This mechanism contributes to understanding the reasons for insensitivity to drug-induced apoptosis and the induction of drug-detoxification by cancer cells. This study has yielded important information about how to circumvent drug resistance to improve cancer chemotherapy. Furthermore, fluorescence microscopy results postulate that induction of MV release with agonist agents and anticancer drugs, results in damage to the host plasma membrane, which must be resealed immediately using activated Iysosomes if the host cell is to survive and proliferate. |
| first_indexed | 2024-07-09T04:04:29Z |
| format | Thesis |
| id | oai:repository.londonmet.ac.uk:7489 |
| institution | London Metropolitan University |
| language | English |
| last_indexed | 2024-07-09T04:04:29Z |
| publishDate | 2012 |
| record_format | eprints |
| spelling | oai:repository.londonmet.ac.uk:74892022-04-25T10:42:50Z http://repository.londonmet.ac.uk/7489/ The role of microvesicles in cancer and viral infection Jorfi, Samireh 610 Medicine & health Microvesicles are shed constitutively, or upon activation from both normal and malignant cells. Although recent studies have reported various nonlytic virus release mechanisms, this mode of virus transmission to secondary sites of infection has remained unclear. This study identified that Coxsackie virus B1 (CVB1) entry into HeLa cells results in apoptosis and production of virus-induced apoptotic microvesicles (vaMVs) by infected cells. Flow cytometery and fluorescence microscopy data illustrated that these vaMVs carry and disseminate CVB1 virions to new host cells via a non lytic MV-to-cell viral mechanism. Inhibition of MV production by siRNA knockdown of CAPNS1 in HeLa cells suggested that these vesicles mediate the spread of apoptosis to secondary sites of infection and the vaMVs could mediate non lytic MV-to-cell transmission. This thesis also identified a new mechanism for multi-drug resistance involving the efflux of anticancer drugs from cancer cells mediated by release of microvesicles, removing the drug from treated cancer cells. Immunoblotting and flow cytometery data showed that transcriptional silencing of calpain by siRNA knockdown of CAPNS1 in PC3M cells prior to drug treatment inhibits MV release and results in induced apoptosis in cells. This mechanism contributes to understanding the reasons for insensitivity to drug-induced apoptosis and the induction of drug-detoxification by cancer cells. This study has yielded important information about how to circumvent drug resistance to improve cancer chemotherapy. Furthermore, fluorescence microscopy results postulate that induction of MV release with agonist agents and anticancer drugs, results in damage to the host plasma membrane, which must be resealed immediately using activated Iysosomes if the host cell is to survive and proliferate. 2012 Thesis NonPeerReviewed text en https://repository.londonmet.ac.uk/7489/1/590129.pdf Jorfi, Samireh (2012) The role of microvesicles in cancer and viral infection. Doctoral thesis, London Metropolitan University. |
| spellingShingle | 610 Medicine & health Jorfi, Samireh The role of microvesicles in cancer and viral infection |
| title | The role of microvesicles in cancer and viral infection |
| title_full | The role of microvesicles in cancer and viral infection |
| title_fullStr | The role of microvesicles in cancer and viral infection |
| title_full_unstemmed | The role of microvesicles in cancer and viral infection |
| title_short | The role of microvesicles in cancer and viral infection |
| title_sort | role of microvesicles in cancer and viral infection |
| topic | 610 Medicine & health |
| url | https://repository.londonmet.ac.uk/7489/1/590129.pdf |
| work_keys_str_mv | AT jorfisamireh theroleofmicrovesiclesincancerandviralinfection AT jorfisamireh roleofmicrovesiclesincancerandviralinfection |