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Engineered NF-κB siRNA-encapsulating exosomes as a modality for therapy of skin lesions
INTRODUCTION: Despite the protection and management of skin has been paid more and more attention, effective countermeasures are still lacking for patients suffering from UV or chemotherapy with damaged skin. Recently, gene therapy by small interfering RNA (siRNA) has emerged as a new therapeutic st...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945116/ https://www.ncbi.nlm.nih.gov/pubmed/36845116 http://dx.doi.org/10.3389/fimmu.2023.1109381 |
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author | Lu, Wei Zhang, Jinzhong Wu, Yungang Sun, Wenxue Jiang, Zipei Luo, Xu |
author_facet | Lu, Wei Zhang, Jinzhong Wu, Yungang Sun, Wenxue Jiang, Zipei Luo, Xu |
author_sort | Lu, Wei |
collection | PubMed |
description | INTRODUCTION: Despite the protection and management of skin has been paid more and more attention, effective countermeasures are still lacking for patients suffering from UV or chemotherapy with damaged skin. Recently, gene therapy by small interfering RNA (siRNA) has emerged as a new therapeutic strategy for skin lesions. However, siRNA therapy has not been applied to skin therapy due to lack of effective delivery vector. METHODS: Here, we develop a synthetic biology strategy that integrates the exosomes with artificial genetic circuits to reprogram the adipose mesenchymal stem cell to express and assemble siRNAs into exosomes and facilitate in vivo delivery siRNAs for therapy of mouse models of skin lesions. RESULTS: Particularly, siRNA enriched exosomes (si-ADMSC-EXOs) could be directly taken up by the skin cells to inhibit the expression of skin injury related genes. When mice with skin lesions were smeared with si-ADMSC-EXOs, the repair of lesioned skin became faster and the expression of inflammatory cytokines were decreased. DISCUSSION: Overall, this study establishes a feasible therapeutic strategy for skin injury, which may offer an alternative to conventional biological therapies requiring two or more independent compounds. |
format | Online Article Text |
id | pubmed-9945116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99451162023-02-23 Engineered NF-κB siRNA-encapsulating exosomes as a modality for therapy of skin lesions Lu, Wei Zhang, Jinzhong Wu, Yungang Sun, Wenxue Jiang, Zipei Luo, Xu Front Immunol Immunology INTRODUCTION: Despite the protection and management of skin has been paid more and more attention, effective countermeasures are still lacking for patients suffering from UV or chemotherapy with damaged skin. Recently, gene therapy by small interfering RNA (siRNA) has emerged as a new therapeutic strategy for skin lesions. However, siRNA therapy has not been applied to skin therapy due to lack of effective delivery vector. METHODS: Here, we develop a synthetic biology strategy that integrates the exosomes with artificial genetic circuits to reprogram the adipose mesenchymal stem cell to express and assemble siRNAs into exosomes and facilitate in vivo delivery siRNAs for therapy of mouse models of skin lesions. RESULTS: Particularly, siRNA enriched exosomes (si-ADMSC-EXOs) could be directly taken up by the skin cells to inhibit the expression of skin injury related genes. When mice with skin lesions were smeared with si-ADMSC-EXOs, the repair of lesioned skin became faster and the expression of inflammatory cytokines were decreased. DISCUSSION: Overall, this study establishes a feasible therapeutic strategy for skin injury, which may offer an alternative to conventional biological therapies requiring two or more independent compounds. Frontiers Media S.A. 2023-02-08 /pmc/articles/PMC9945116/ /pubmed/36845116 http://dx.doi.org/10.3389/fimmu.2023.1109381 Text en Copyright © 2023 Lu, Zhang, Wu, Sun, Jiang and Luo https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Lu, Wei Zhang, Jinzhong Wu, Yungang Sun, Wenxue Jiang, Zipei Luo, Xu Engineered NF-κB siRNA-encapsulating exosomes as a modality for therapy of skin lesions |
title | Engineered NF-κB siRNA-encapsulating exosomes as a modality for therapy of skin lesions |
title_full | Engineered NF-κB siRNA-encapsulating exosomes as a modality for therapy of skin lesions |
title_fullStr | Engineered NF-κB siRNA-encapsulating exosomes as a modality for therapy of skin lesions |
title_full_unstemmed | Engineered NF-κB siRNA-encapsulating exosomes as a modality for therapy of skin lesions |
title_short | Engineered NF-κB siRNA-encapsulating exosomes as a modality for therapy of skin lesions |
title_sort | engineered nf-κb sirna-encapsulating exosomes as a modality for therapy of skin lesions |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945116/ https://www.ncbi.nlm.nih.gov/pubmed/36845116 http://dx.doi.org/10.3389/fimmu.2023.1109381 |
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