Lentiviral gene delivery to plasmolipin-expressing cells using Mus caroli endogenous retrovirus envelope protein

Gene therapy is a promising method for treating malignant diseases. One of the main problems is target delivery of therapeutic genes. Here we show that lentiviral vector particles pseudotyped with Mus caroli endogenous retrovirus (McERV) envelope protein can be used for selective transduction of PLL...

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Veröffentlicht in:Biochimie 2017-11, Vol.142, p.226-233
Hauptverfasser: Prokofjeva, M.M., Proshkina, G.M., Lebedev, T.D., Shulgin, A.A., Spirin, P.V., Prassolov, V.S., Deyev, S.M.
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container_start_page 226
container_title Biochimie
container_volume 142
creator Prokofjeva, M.M.
Proshkina, G.M.
Lebedev, T.D.
Shulgin, A.A.
Spirin, P.V.
Prassolov, V.S.
Deyev, S.M.
description Gene therapy is a promising method for treating malignant diseases. One of the main problems is target delivery of therapeutic genes. Here we show that lentiviral vector particles pseudotyped with Mus caroli endogenous retrovirus (McERV) envelope protein can be used for selective transduction of PLLP-expressing cells. As a therapeutic gene in McERV-pseudotyped vector particles we used miniSOG encoding the cytotoxic FMN-binding protein, which can generate reactive oxygen species under illumination. Significant cytotoxic effect (up to 80% of dead cells in population) was observed in PLLP-expressing cells transduced with McERV-pseudotyped vector particles and subjected to illumination. We demonstrated that the McERV-pseudotyped HIV-1 based lentiviral vector particles are an effective tool for selective photoinduced destruction of PLLP-expressing cells. •A lentiviral system for gene delivery using envelope protein that target tissue-specific protein plasmolipin is introduced.•A genetically encoded photosensitizer miniSOG is used as a therapeutic gene.•PLLP-positive malignant neural cells transduced with lentiviral particles and illuminated by blue light are destroyed.
doi_str_mv 10.1016/j.biochi.2017.09.004
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One of the main problems is target delivery of therapeutic genes. Here we show that lentiviral vector particles pseudotyped with Mus caroli endogenous retrovirus (McERV) envelope protein can be used for selective transduction of PLLP-expressing cells. As a therapeutic gene in McERV-pseudotyped vector particles we used miniSOG encoding the cytotoxic FMN-binding protein, which can generate reactive oxygen species under illumination. Significant cytotoxic effect (up to 80% of dead cells in population) was observed in PLLP-expressing cells transduced with McERV-pseudotyped vector particles and subjected to illumination. 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subjects Animals
Blue light illumination
cytotoxicity
Endogenous Retroviruses
Gene delivery
Gene Expression
gene therapy
gene transfer
Gene Transfer Techniques
genes
HEK293 Cells
Humans
Lentiviral vectors
Lentivirus - genetics
lighting
Mice
miniSOG
Myelin and Lymphocyte-Associated Proteolipid Proteins - genetics
Photoinduced cytotoxicity
Plasmolipin
reactive oxygen species
Retroviridae
Transduction, Genetic
Viral Proteins - metabolism
title Lentiviral gene delivery to plasmolipin-expressing cells using Mus caroli endogenous retrovirus envelope protein
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