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Thermoresponsive Bacteriophage Nanocarrier as a Gene Delivery Vector Targeted to the Gastrointestinal Tract

The use of the gastrointestinal tract as a site for the local delivery of DNA is an exciting prospect. In order to obtain an effective vector capable of delivering a gene of interest to target cells to achieve sufficient and sustained transgene expression, with minimal toxicity, we developed a new g...

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Autores principales: Namdee, Katawut, Khongkow, Mattaka, Boonrungsiman, Suwimon, Nittayasut, Naiyaphat, Asavarut, Paladd, Temisak, Sasithon, Saengkrit, Nattika, Puttipipatkhachorn, Satit, Hajitou, Amin, Ruxrungtham, Kiat, Yata, Teerapong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023791/
https://www.ncbi.nlm.nih.gov/pubmed/30195771
http://dx.doi.org/10.1016/j.omtn.2018.04.012
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author Namdee, Katawut
Khongkow, Mattaka
Boonrungsiman, Suwimon
Nittayasut, Naiyaphat
Asavarut, Paladd
Temisak, Sasithon
Saengkrit, Nattika
Puttipipatkhachorn, Satit
Hajitou, Amin
Ruxrungtham, Kiat
Yata, Teerapong
author_facet Namdee, Katawut
Khongkow, Mattaka
Boonrungsiman, Suwimon
Nittayasut, Naiyaphat
Asavarut, Paladd
Temisak, Sasithon
Saengkrit, Nattika
Puttipipatkhachorn, Satit
Hajitou, Amin
Ruxrungtham, Kiat
Yata, Teerapong
author_sort Namdee, Katawut
collection PubMed
description The use of the gastrointestinal tract as a site for the local delivery of DNA is an exciting prospect. In order to obtain an effective vector capable of delivering a gene of interest to target cells to achieve sufficient and sustained transgene expression, with minimal toxicity, we developed a new generation of filamentous bacteriophage. This particular bacteriophage was genetically engineered to display an arginine-glycine-aspartic acid (RGD) motif (an integrin-binding peptide) on the major coat protein pVIII and carry a mammalian DNA cassette. One unanticipated observation is the thermoresponsive behavior of engineered bacteriophage. This finding has led us to simplify the isolation method to purify bacteriophage particles from cell culture supernatant by low-temperature precipitation. Our results showed that, in contrast to non-surface modified, the RGD-modified bacteriophage was successfully used to deliver a transgene to mammalian cells. Our in vitro model of the human intestinal follicle-associated epithelium also demonstrated that bacteriophage particles were stable in simulated gastrointestinal fluids and able to cross the human intestinal barrier. In addition, we confirmed an adjuvant property of the engineered bacteriophage to induce nitric oxide production by macrophages. In conclusion, our study demonstrated the possibility of using bacteriophage for gene transfer in the gastrointestinal tract.
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spelling pubmed-60237912018-06-29 Thermoresponsive Bacteriophage Nanocarrier as a Gene Delivery Vector Targeted to the Gastrointestinal Tract Namdee, Katawut Khongkow, Mattaka Boonrungsiman, Suwimon Nittayasut, Naiyaphat Asavarut, Paladd Temisak, Sasithon Saengkrit, Nattika Puttipipatkhachorn, Satit Hajitou, Amin Ruxrungtham, Kiat Yata, Teerapong Mol Ther Nucleic Acids Article The use of the gastrointestinal tract as a site for the local delivery of DNA is an exciting prospect. In order to obtain an effective vector capable of delivering a gene of interest to target cells to achieve sufficient and sustained transgene expression, with minimal toxicity, we developed a new generation of filamentous bacteriophage. This particular bacteriophage was genetically engineered to display an arginine-glycine-aspartic acid (RGD) motif (an integrin-binding peptide) on the major coat protein pVIII and carry a mammalian DNA cassette. One unanticipated observation is the thermoresponsive behavior of engineered bacteriophage. This finding has led us to simplify the isolation method to purify bacteriophage particles from cell culture supernatant by low-temperature precipitation. Our results showed that, in contrast to non-surface modified, the RGD-modified bacteriophage was successfully used to deliver a transgene to mammalian cells. Our in vitro model of the human intestinal follicle-associated epithelium also demonstrated that bacteriophage particles were stable in simulated gastrointestinal fluids and able to cross the human intestinal barrier. In addition, we confirmed an adjuvant property of the engineered bacteriophage to induce nitric oxide production by macrophages. In conclusion, our study demonstrated the possibility of using bacteriophage for gene transfer in the gastrointestinal tract. American Society of Gene & Cell Therapy 2018-05-01 /pmc/articles/PMC6023791/ /pubmed/30195771 http://dx.doi.org/10.1016/j.omtn.2018.04.012 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Namdee, Katawut
Khongkow, Mattaka
Boonrungsiman, Suwimon
Nittayasut, Naiyaphat
Asavarut, Paladd
Temisak, Sasithon
Saengkrit, Nattika
Puttipipatkhachorn, Satit
Hajitou, Amin
Ruxrungtham, Kiat
Yata, Teerapong
Thermoresponsive Bacteriophage Nanocarrier as a Gene Delivery Vector Targeted to the Gastrointestinal Tract
title Thermoresponsive Bacteriophage Nanocarrier as a Gene Delivery Vector Targeted to the Gastrointestinal Tract
title_full Thermoresponsive Bacteriophage Nanocarrier as a Gene Delivery Vector Targeted to the Gastrointestinal Tract
title_fullStr Thermoresponsive Bacteriophage Nanocarrier as a Gene Delivery Vector Targeted to the Gastrointestinal Tract
title_full_unstemmed Thermoresponsive Bacteriophage Nanocarrier as a Gene Delivery Vector Targeted to the Gastrointestinal Tract
title_short Thermoresponsive Bacteriophage Nanocarrier as a Gene Delivery Vector Targeted to the Gastrointestinal Tract
title_sort thermoresponsive bacteriophage nanocarrier as a gene delivery vector targeted to the gastrointestinal tract
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023791/
https://www.ncbi.nlm.nih.gov/pubmed/30195771
http://dx.doi.org/10.1016/j.omtn.2018.04.012
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