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Efficient gene delivery and silencing of mouse and human pancreatic islets
BACKGROUND: In view of the importance of beta cells in glucose homeostasis and the profound repercussions of beta cell pathology on human health, the acquisition of tools to study pancreatic islet function is essential for the design of alternative novel therapies for diabetes. One promising approac...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853492/ https://www.ncbi.nlm.nih.gov/pubmed/20353585 http://dx.doi.org/10.1186/1472-6750-10-28 |
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author | Lefebvre, Bruno Vandewalle, Brigitte Longue, Justine Moerman, Ericka Lukowiak, Bruno Gmyr, Valery Maedler, Kathrin Kerr-conte, Julie Pattou, François |
author_facet | Lefebvre, Bruno Vandewalle, Brigitte Longue, Justine Moerman, Ericka Lukowiak, Bruno Gmyr, Valery Maedler, Kathrin Kerr-conte, Julie Pattou, François |
author_sort | Lefebvre, Bruno |
collection | PubMed |
description | BACKGROUND: In view of the importance of beta cells in glucose homeostasis and the profound repercussions of beta cell pathology on human health, the acquisition of tools to study pancreatic islet function is essential for the design of alternative novel therapies for diabetes. One promising approach toward this goal involves the modification of gene expression profile of beta cells. RESULTS: This study describes a new method of gene and siRNA delivery into human pancreatic islets by microporation technology. We demonstrated that mild islet distention with accutase greatly enhanced the transfection efficiency without compromising in vitro function (secretion, apoptosis and viability). As an example, the recently identified gene involved in type 2 diabetes, ZnT8, can be over-expressed or silenced by RNA interference using this technology. Microporation can also be used on rodent islets. CONCLUSIONS: Taken together, our results demonstrate that microporation technology can be used to modify gene expression in whole rodent and human islets without altering their in vitro function and will be key to the elucidation of the factors responsible for proper islet function. |
format | Text |
id | pubmed-2853492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28534922010-04-13 Efficient gene delivery and silencing of mouse and human pancreatic islets Lefebvre, Bruno Vandewalle, Brigitte Longue, Justine Moerman, Ericka Lukowiak, Bruno Gmyr, Valery Maedler, Kathrin Kerr-conte, Julie Pattou, François BMC Biotechnol Methodology article BACKGROUND: In view of the importance of beta cells in glucose homeostasis and the profound repercussions of beta cell pathology on human health, the acquisition of tools to study pancreatic islet function is essential for the design of alternative novel therapies for diabetes. One promising approach toward this goal involves the modification of gene expression profile of beta cells. RESULTS: This study describes a new method of gene and siRNA delivery into human pancreatic islets by microporation technology. We demonstrated that mild islet distention with accutase greatly enhanced the transfection efficiency without compromising in vitro function (secretion, apoptosis and viability). As an example, the recently identified gene involved in type 2 diabetes, ZnT8, can be over-expressed or silenced by RNA interference using this technology. Microporation can also be used on rodent islets. CONCLUSIONS: Taken together, our results demonstrate that microporation technology can be used to modify gene expression in whole rodent and human islets without altering their in vitro function and will be key to the elucidation of the factors responsible for proper islet function. BioMed Central 2010-03-30 /pmc/articles/PMC2853492/ /pubmed/20353585 http://dx.doi.org/10.1186/1472-6750-10-28 Text en Copyright ©2010 Lefebvre et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology article Lefebvre, Bruno Vandewalle, Brigitte Longue, Justine Moerman, Ericka Lukowiak, Bruno Gmyr, Valery Maedler, Kathrin Kerr-conte, Julie Pattou, François Efficient gene delivery and silencing of mouse and human pancreatic islets |
title | Efficient gene delivery and silencing of mouse and human pancreatic islets |
title_full | Efficient gene delivery and silencing of mouse and human pancreatic islets |
title_fullStr | Efficient gene delivery and silencing of mouse and human pancreatic islets |
title_full_unstemmed | Efficient gene delivery and silencing of mouse and human pancreatic islets |
title_short | Efficient gene delivery and silencing of mouse and human pancreatic islets |
title_sort | efficient gene delivery and silencing of mouse and human pancreatic islets |
topic | Methodology article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853492/ https://www.ncbi.nlm.nih.gov/pubmed/20353585 http://dx.doi.org/10.1186/1472-6750-10-28 |
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