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Optimizing NTS-Polyplex as a Tool for Gene Transfer to Cultured Dopamine Neurons

The study of signal transduction in dopamine (DA)-containing neurons as well as the development of new therapeutic approaches for Parkinson's disease requires the selective expression of transgenes in such neurons. Here we describe optimization of the use of the NTS-polyplex, a gene carrier sys...

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Autores principales: Hernandez-Baltazar, Daniel, Martinez-Fong, Daniel, Trudeau, Louis-Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530538/
https://www.ncbi.nlm.nih.gov/pubmed/23300540
http://dx.doi.org/10.1371/journal.pone.0051341
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author Hernandez-Baltazar, Daniel
Martinez-Fong, Daniel
Trudeau, Louis-Eric
author_facet Hernandez-Baltazar, Daniel
Martinez-Fong, Daniel
Trudeau, Louis-Eric
author_sort Hernandez-Baltazar, Daniel
collection PubMed
description The study of signal transduction in dopamine (DA)-containing neurons as well as the development of new therapeutic approaches for Parkinson's disease requires the selective expression of transgenes in such neurons. Here we describe optimization of the use of the NTS-polyplex, a gene carrier system taking advantage of neurotensin receptor internalization, to transfect mouse DA neurons in primary culture. The plasmids DsRed2 (4.7 kbp) and VGLUT2-Venus (11 kbp) were used to compare the ability of this carrier system to transfect plasmids of different sizes. We examined the impact of age of the neurons (1, 3, 5 and 8 days after seeding), of culture media used during the transfection (Neurobasal with B27 vs. conditioned medium) and of three molar ratios of plasmid DNA to carrier. While the NTS-polyplex successfully transfected both plasmids in a control N1E-115 cell line, only the pDsRed2 plasmid could be transfected in primary cultured DA neurons. We achieved 20% transfection efficiency of pDsRed2 in DA neurons, with 80% cell viability. The transfection was demonstrated pharmacologically to be dependent on activation of neurotensin receptors and to be selective for DA neurons. The presence of conditioned medium for transfection was found to be required to insure cell viability. Highest transfection efficiency was achieved in the most mature neurons. In contrast, transfection with the VGLUT2-Venus plasmid produced cell damage, most likely due to the high molar ratios required, as evidenced by a 15% cell viability of DA neurons at the three molar ratios tested (1∶36, 1∶39 and 1∶42). We conclude that, when used at molar ratios lower than 1∶33, the NTS-polyplex can selectively transfect mature cultured DA neurons with only low levels of toxicity. Our results provide evidence that the NTS-polyplex has good potential for targeted gene delivery in cultured DA neurons, an in vitro system of great use for the screening of new therapeutic approaches for Parkinson's disease.
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spelling pubmed-35305382013-01-08 Optimizing NTS-Polyplex as a Tool for Gene Transfer to Cultured Dopamine Neurons Hernandez-Baltazar, Daniel Martinez-Fong, Daniel Trudeau, Louis-Eric PLoS One Research Article The study of signal transduction in dopamine (DA)-containing neurons as well as the development of new therapeutic approaches for Parkinson's disease requires the selective expression of transgenes in such neurons. Here we describe optimization of the use of the NTS-polyplex, a gene carrier system taking advantage of neurotensin receptor internalization, to transfect mouse DA neurons in primary culture. The plasmids DsRed2 (4.7 kbp) and VGLUT2-Venus (11 kbp) were used to compare the ability of this carrier system to transfect plasmids of different sizes. We examined the impact of age of the neurons (1, 3, 5 and 8 days after seeding), of culture media used during the transfection (Neurobasal with B27 vs. conditioned medium) and of three molar ratios of plasmid DNA to carrier. While the NTS-polyplex successfully transfected both plasmids in a control N1E-115 cell line, only the pDsRed2 plasmid could be transfected in primary cultured DA neurons. We achieved 20% transfection efficiency of pDsRed2 in DA neurons, with 80% cell viability. The transfection was demonstrated pharmacologically to be dependent on activation of neurotensin receptors and to be selective for DA neurons. The presence of conditioned medium for transfection was found to be required to insure cell viability. Highest transfection efficiency was achieved in the most mature neurons. In contrast, transfection with the VGLUT2-Venus plasmid produced cell damage, most likely due to the high molar ratios required, as evidenced by a 15% cell viability of DA neurons at the three molar ratios tested (1∶36, 1∶39 and 1∶42). We conclude that, when used at molar ratios lower than 1∶33, the NTS-polyplex can selectively transfect mature cultured DA neurons with only low levels of toxicity. Our results provide evidence that the NTS-polyplex has good potential for targeted gene delivery in cultured DA neurons, an in vitro system of great use for the screening of new therapeutic approaches for Parkinson's disease. Public Library of Science 2012-12-26 /pmc/articles/PMC3530538/ /pubmed/23300540 http://dx.doi.org/10.1371/journal.pone.0051341 Text en © 2012 Hernandez-Baltazar et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hernandez-Baltazar, Daniel
Martinez-Fong, Daniel
Trudeau, Louis-Eric
Optimizing NTS-Polyplex as a Tool for Gene Transfer to Cultured Dopamine Neurons
title Optimizing NTS-Polyplex as a Tool for Gene Transfer to Cultured Dopamine Neurons
title_full Optimizing NTS-Polyplex as a Tool for Gene Transfer to Cultured Dopamine Neurons
title_fullStr Optimizing NTS-Polyplex as a Tool for Gene Transfer to Cultured Dopamine Neurons
title_full_unstemmed Optimizing NTS-Polyplex as a Tool for Gene Transfer to Cultured Dopamine Neurons
title_short Optimizing NTS-Polyplex as a Tool for Gene Transfer to Cultured Dopamine Neurons
title_sort optimizing nts-polyplex as a tool for gene transfer to cultured dopamine neurons
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530538/
https://www.ncbi.nlm.nih.gov/pubmed/23300540
http://dx.doi.org/10.1371/journal.pone.0051341
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