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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...

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Autores principales: Lefebvre, Bruno, Vandewalle, Brigitte, Longue, Justine, Moerman, Ericka, Lukowiak, Bruno, Gmyr, Valery, Maedler, Kathrin, Kerr-conte, Julie, Pattou, François
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
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.
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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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