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Size Specific Transfection to Mammalian Cells by Micropillar Array Electroporation
Electroporation serves as a promising non-viral gene delivery approach, while its current configuration carries several drawbacks associated with high-voltage electrical pulses and heterogeneous treatment on individual cells. Here we developed a new micropillar array electroporation (MAE) platform t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5141490/ https://www.ncbi.nlm.nih.gov/pubmed/27924861 http://dx.doi.org/10.1038/srep38661 |
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author | Zu, Yingbo Huang, Shuyan Lu, Yang Liu, Xuan Wang, Shengnian |
author_facet | Zu, Yingbo Huang, Shuyan Lu, Yang Liu, Xuan Wang, Shengnian |
author_sort | Zu, Yingbo |
collection | PubMed |
description | Electroporation serves as a promising non-viral gene delivery approach, while its current configuration carries several drawbacks associated with high-voltage electrical pulses and heterogeneous treatment on individual cells. Here we developed a new micropillar array electroporation (MAE) platform to advance the electroporation-based delivery of DNA and RNA probes into mammalian cells. By introducing well-patterned micropillar array texture on the electrode surface, the number of pillars each cell faces varies with its plasma membrane surface area, despite their large population and random locations. In this way, cell size specific electroporation is conveniently carried out, contributing to a 2.5~3 fold increase on plasmid DNA transfection and an additional 10–55% transgene knockdown with siRNA probes, respectively. The delivery efficiency varies with the number and size of micropillars as well as their pattern density. As MAE works like many single cell electroporation are carried out in parallel, the electrophysiology response of individual cells is representative, which has potentials to facilitate the tedious, cell-specific protocol screening process in current bulk electroporation (i.e., electroporation to a large population of cells). Its success might promote the wide adoption of electroporation as a safe and effective non-viral gene delivery approach needed in many biological research and clinical treatments. |
format | Online Article Text |
id | pubmed-5141490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51414902016-12-16 Size Specific Transfection to Mammalian Cells by Micropillar Array Electroporation Zu, Yingbo Huang, Shuyan Lu, Yang Liu, Xuan Wang, Shengnian Sci Rep Article Electroporation serves as a promising non-viral gene delivery approach, while its current configuration carries several drawbacks associated with high-voltage electrical pulses and heterogeneous treatment on individual cells. Here we developed a new micropillar array electroporation (MAE) platform to advance the electroporation-based delivery of DNA and RNA probes into mammalian cells. By introducing well-patterned micropillar array texture on the electrode surface, the number of pillars each cell faces varies with its plasma membrane surface area, despite their large population and random locations. In this way, cell size specific electroporation is conveniently carried out, contributing to a 2.5~3 fold increase on plasmid DNA transfection and an additional 10–55% transgene knockdown with siRNA probes, respectively. The delivery efficiency varies with the number and size of micropillars as well as their pattern density. As MAE works like many single cell electroporation are carried out in parallel, the electrophysiology response of individual cells is representative, which has potentials to facilitate the tedious, cell-specific protocol screening process in current bulk electroporation (i.e., electroporation to a large population of cells). Its success might promote the wide adoption of electroporation as a safe and effective non-viral gene delivery approach needed in many biological research and clinical treatments. Nature Publishing Group 2016-12-07 /pmc/articles/PMC5141490/ /pubmed/27924861 http://dx.doi.org/10.1038/srep38661 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zu, Yingbo Huang, Shuyan Lu, Yang Liu, Xuan Wang, Shengnian Size Specific Transfection to Mammalian Cells by Micropillar Array Electroporation |
title | Size Specific Transfection to Mammalian Cells by Micropillar Array Electroporation |
title_full | Size Specific Transfection to Mammalian Cells by Micropillar Array Electroporation |
title_fullStr | Size Specific Transfection to Mammalian Cells by Micropillar Array Electroporation |
title_full_unstemmed | Size Specific Transfection to Mammalian Cells by Micropillar Array Electroporation |
title_short | Size Specific Transfection to Mammalian Cells by Micropillar Array Electroporation |
title_sort | size specific transfection to mammalian cells by micropillar array electroporation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5141490/ https://www.ncbi.nlm.nih.gov/pubmed/27924861 http://dx.doi.org/10.1038/srep38661 |
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