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High Efficiency Low Cost Fibroblast Nucleofection for GMP Compatible Cell-based Gene Therapy
Background: Dermal fibroblast is a powerful tool for the study of ex vivo DNA delivery in development of both cell therapy and tissue engineering products. Using genetic modification, fibroblasts can be diversely adapted and made suitable for clinical gene therapy. In this study, we first compared s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562186/ https://www.ncbi.nlm.nih.gov/pubmed/28824316 http://dx.doi.org/10.7150/ijms.19241 |
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author | Zhang, Ziyang Slobodianski, Alex Arnold, Astrid Nehlsen, Jessica Hopfner, Ursula Schilling, Arndt F. Perisic, Tatjana Machens, Hans-Günther |
author_facet | Zhang, Ziyang Slobodianski, Alex Arnold, Astrid Nehlsen, Jessica Hopfner, Ursula Schilling, Arndt F. Perisic, Tatjana Machens, Hans-Günther |
author_sort | Zhang, Ziyang |
collection | PubMed |
description | Background: Dermal fibroblast is a powerful tool for the study of ex vivo DNA delivery in development of both cell therapy and tissue engineering products. Using genetic modification, fibroblasts can be diversely adapted and made suitable for clinical gene therapy. In this study, we first compared several non-viral transfection methods including nucleofection in rat and human primary dermal fibroblast. In addition, the original protocol for nucleofection of primary mammalian fibroblasts was modified in order to achieve the highest possible transfection efficiency, as determined by flow cytometry analysis of the green fluorescent protein (GFP) expression. Results: the results showed that transfection performance of Dulbecco's Modified Eagle Medium (DMEM) supplemented with 10% Fetal Calf Serum (FCS) yielded the best transfection efficiency with rat dermal fibroblasts and ITS (insulin, transferrin, and sodium selenite solution) was comparable to the standard nucleofection solution for human dermal fibroblasts. Conclusion: Our results suggest a promising application of the modified nucleofection method for GMP compatible therapeutic translational medical research. |
format | Online Article Text |
id | pubmed-5562186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-55621862017-08-18 High Efficiency Low Cost Fibroblast Nucleofection for GMP Compatible Cell-based Gene Therapy Zhang, Ziyang Slobodianski, Alex Arnold, Astrid Nehlsen, Jessica Hopfner, Ursula Schilling, Arndt F. Perisic, Tatjana Machens, Hans-Günther Int J Med Sci Short Research Communication Background: Dermal fibroblast is a powerful tool for the study of ex vivo DNA delivery in development of both cell therapy and tissue engineering products. Using genetic modification, fibroblasts can be diversely adapted and made suitable for clinical gene therapy. In this study, we first compared several non-viral transfection methods including nucleofection in rat and human primary dermal fibroblast. In addition, the original protocol for nucleofection of primary mammalian fibroblasts was modified in order to achieve the highest possible transfection efficiency, as determined by flow cytometry analysis of the green fluorescent protein (GFP) expression. Results: the results showed that transfection performance of Dulbecco's Modified Eagle Medium (DMEM) supplemented with 10% Fetal Calf Serum (FCS) yielded the best transfection efficiency with rat dermal fibroblasts and ITS (insulin, transferrin, and sodium selenite solution) was comparable to the standard nucleofection solution for human dermal fibroblasts. Conclusion: Our results suggest a promising application of the modified nucleofection method for GMP compatible therapeutic translational medical research. Ivyspring International Publisher 2017-07-19 /pmc/articles/PMC5562186/ /pubmed/28824316 http://dx.doi.org/10.7150/ijms.19241 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Short Research Communication Zhang, Ziyang Slobodianski, Alex Arnold, Astrid Nehlsen, Jessica Hopfner, Ursula Schilling, Arndt F. Perisic, Tatjana Machens, Hans-Günther High Efficiency Low Cost Fibroblast Nucleofection for GMP Compatible Cell-based Gene Therapy |
title | High Efficiency Low Cost Fibroblast Nucleofection for GMP Compatible Cell-based Gene Therapy |
title_full | High Efficiency Low Cost Fibroblast Nucleofection for GMP Compatible Cell-based Gene Therapy |
title_fullStr | High Efficiency Low Cost Fibroblast Nucleofection for GMP Compatible Cell-based Gene Therapy |
title_full_unstemmed | High Efficiency Low Cost Fibroblast Nucleofection for GMP Compatible Cell-based Gene Therapy |
title_short | High Efficiency Low Cost Fibroblast Nucleofection for GMP Compatible Cell-based Gene Therapy |
title_sort | high efficiency low cost fibroblast nucleofection for gmp compatible cell-based gene therapy |
topic | Short Research Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562186/ https://www.ncbi.nlm.nih.gov/pubmed/28824316 http://dx.doi.org/10.7150/ijms.19241 |
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