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Intradermal Delivery of Synthetic mRNA Using Hollow Microneedles for Efficient and Rapid Production of Exogenous Proteins in Skin

In recent years, synthetic mRNA-based applications to produce desired exogenous proteins in cells have been gaining importance. However, systemic delivery of synthetic mRNA can result in unspecific uptake into undesired cells or organs and, thereby, fail to target desired cells. Thus, local and targ...

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Autores principales: Golombek, Sonia, Pilz, Martin, Steinle, Heidrun, Kochba, Efrat, Levin, Yotam, Lunter, Dominique, Schlensak, Christian, Wendel, Hans Peter, Avci-Adali, Meltem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992458/
https://www.ncbi.nlm.nih.gov/pubmed/29858073
http://dx.doi.org/10.1016/j.omtn.2018.03.005
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author Golombek, Sonia
Pilz, Martin
Steinle, Heidrun
Kochba, Efrat
Levin, Yotam
Lunter, Dominique
Schlensak, Christian
Wendel, Hans Peter
Avci-Adali, Meltem
author_facet Golombek, Sonia
Pilz, Martin
Steinle, Heidrun
Kochba, Efrat
Levin, Yotam
Lunter, Dominique
Schlensak, Christian
Wendel, Hans Peter
Avci-Adali, Meltem
author_sort Golombek, Sonia
collection PubMed
description In recent years, synthetic mRNA-based applications to produce desired exogenous proteins in cells have been gaining importance. However, systemic delivery of synthetic mRNA can result in unspecific uptake into undesired cells or organs and, thereby, fail to target desired cells. Thus, local and targeted delivery of synthetic mRNA becomes increasingly important to reach the desired cell types and tissues. In this study, intradermal delivery of synthetic mRNA using a hollow microneedle injection-based method was evaluated. Furthermore, an ex vivo porcine skin model was established to analyze synthetic mRNA-mediated protein expression in the skin following intradermal delivery. Using this model, highly efficient delivery of synthetic mRNA was demonstrated, which resulted in detection of high levels of secretable humanized Gaussia luciferase (hGLuc) protein encoded by the microinjected synthetic mRNA. Interestingly, synthetic mRNA injected without transfection reagent was also able to enter the cells and resulted in protein expression. The established ex vivo porcine skin model can be used to evaluate the successful production of desired proteins after intradermal delivery of synthetic mRNAs before starting with in vivo experiments. Furthermore, the use of microneedles enables patient-friendly, painless, and efficient delivery of synthetic mRNAs into the dermis; thus, this method could be applied for local treatment of different skin diseases as well as for vaccination and immunotherapy.
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spelling pubmed-59924582018-06-11 Intradermal Delivery of Synthetic mRNA Using Hollow Microneedles for Efficient and Rapid Production of Exogenous Proteins in Skin Golombek, Sonia Pilz, Martin Steinle, Heidrun Kochba, Efrat Levin, Yotam Lunter, Dominique Schlensak, Christian Wendel, Hans Peter Avci-Adali, Meltem Mol Ther Nucleic Acids Article In recent years, synthetic mRNA-based applications to produce desired exogenous proteins in cells have been gaining importance. However, systemic delivery of synthetic mRNA can result in unspecific uptake into undesired cells or organs and, thereby, fail to target desired cells. Thus, local and targeted delivery of synthetic mRNA becomes increasingly important to reach the desired cell types and tissues. In this study, intradermal delivery of synthetic mRNA using a hollow microneedle injection-based method was evaluated. Furthermore, an ex vivo porcine skin model was established to analyze synthetic mRNA-mediated protein expression in the skin following intradermal delivery. Using this model, highly efficient delivery of synthetic mRNA was demonstrated, which resulted in detection of high levels of secretable humanized Gaussia luciferase (hGLuc) protein encoded by the microinjected synthetic mRNA. Interestingly, synthetic mRNA injected without transfection reagent was also able to enter the cells and resulted in protein expression. The established ex vivo porcine skin model can be used to evaluate the successful production of desired proteins after intradermal delivery of synthetic mRNAs before starting with in vivo experiments. Furthermore, the use of microneedles enables patient-friendly, painless, and efficient delivery of synthetic mRNAs into the dermis; thus, this method could be applied for local treatment of different skin diseases as well as for vaccination and immunotherapy. American Society of Gene & Cell Therapy 2018-03-14 /pmc/articles/PMC5992458/ /pubmed/29858073 http://dx.doi.org/10.1016/j.omtn.2018.03.005 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Golombek, Sonia
Pilz, Martin
Steinle, Heidrun
Kochba, Efrat
Levin, Yotam
Lunter, Dominique
Schlensak, Christian
Wendel, Hans Peter
Avci-Adali, Meltem
Intradermal Delivery of Synthetic mRNA Using Hollow Microneedles for Efficient and Rapid Production of Exogenous Proteins in Skin
title Intradermal Delivery of Synthetic mRNA Using Hollow Microneedles for Efficient and Rapid Production of Exogenous Proteins in Skin
title_full Intradermal Delivery of Synthetic mRNA Using Hollow Microneedles for Efficient and Rapid Production of Exogenous Proteins in Skin
title_fullStr Intradermal Delivery of Synthetic mRNA Using Hollow Microneedles for Efficient and Rapid Production of Exogenous Proteins in Skin
title_full_unstemmed Intradermal Delivery of Synthetic mRNA Using Hollow Microneedles for Efficient and Rapid Production of Exogenous Proteins in Skin
title_short Intradermal Delivery of Synthetic mRNA Using Hollow Microneedles for Efficient and Rapid Production of Exogenous Proteins in Skin
title_sort intradermal delivery of synthetic mrna using hollow microneedles for efficient and rapid production of exogenous proteins in skin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992458/
https://www.ncbi.nlm.nih.gov/pubmed/29858073
http://dx.doi.org/10.1016/j.omtn.2018.03.005
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