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Ultrasound triggered topical delivery of Bmp7 mRNA for white fat browning induction via engineered smart exosomes

BACKGROUND: Efficient and topical delivery of drugs is essential for maximized efficacy and minimized toxicity. In this study, we aimed to design an exosome-based drug delivery platform endowed with the ability of escaping from phagocytosis at non-target organs and controllably releasing drugs at ta...

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Autores principales: Guo, Yitong, Wan, Zhuo, Zhao, Ping, Wei, Mengying, Liu, Yunnan, Bu, Te, Sun, Wenqi, Li, Zhelong, Yuan, Lijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645082/
https://www.ncbi.nlm.nih.gov/pubmed/34863187
http://dx.doi.org/10.1186/s12951-021-01145-3
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author Guo, Yitong
Wan, Zhuo
Zhao, Ping
Wei, Mengying
Liu, Yunnan
Bu, Te
Sun, Wenqi
Li, Zhelong
Yuan, Lijun
author_facet Guo, Yitong
Wan, Zhuo
Zhao, Ping
Wei, Mengying
Liu, Yunnan
Bu, Te
Sun, Wenqi
Li, Zhelong
Yuan, Lijun
author_sort Guo, Yitong
collection PubMed
description BACKGROUND: Efficient and topical delivery of drugs is essential for maximized efficacy and minimized toxicity. In this study, we aimed to design an exosome-based drug delivery platform endowed with the ability of escaping from phagocytosis at non-target organs and controllably releasing drugs at targeted location. RESULTS: The swtichable stealth coat CP05-TK-mPEG was synthesized and anchored onto exosomes through the interaction between peptide CP05 and exosomal surface marker CD63. Chlorin e6 (Ce6) was loaded into exosomes by direct incubation. Controllable removal of PEG could be achieved by breaking thioketal (TK) through reactive oxygen species (ROS), which was produced by Ce6 under ultrasound irradiation. The whole platform was called SmartExo. The stealth effects were analyzed in RAW264.7 cells and C57BL/6 mice via tracing the exosomes. To confirm the efficacy of the engineered smart exosomes, Bone morphogenetic protein 7 (Bmp7) mRNA was encapsulated into exosomes by transfection of overexpressing plasmid, followed by stealth coating, with the exosomes designated as SmartExo@Bmp7. Therapeutic advantages of SmartExo@Bmp7 were proved by targeted delivering Bmp7 mRNA to omental adipose tissue (OAT) of obese C57BL/6 mice for browning induction. SmartExo platform was successfully constructed without changing the basic characteristics of exosomes. The engineered exosomes effectively escaped from the phagocytosis by RAW264.7 and non-target organs. In addition, the SmartExo could be uptaken locally on-demand by ultrasound mediated removal of the stealth coat. Compared with control exosomes, SmartExo@Bmp7 effectively delivered Bmp7 mRNA into OAT upon ultrasound irradiation, and induced OAT browning, as evidenced by the histology of OAT and increased expression of uncoupling protein 1 (Ucp1). CONCLUSIONS: The proposed SmartExo-based delivery platform, which minimizes side effects and maximizing drug efficacy, offers a novel safe and efficient approach for targeted drug delivery. As a proof, the SmartExo@Bmp7 induced local white adipose tissue browning, and it would be a promising strategy for anti-obesity therapy. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-01145-3.
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spelling pubmed-86450822021-12-06 Ultrasound triggered topical delivery of Bmp7 mRNA for white fat browning induction via engineered smart exosomes Guo, Yitong Wan, Zhuo Zhao, Ping Wei, Mengying Liu, Yunnan Bu, Te Sun, Wenqi Li, Zhelong Yuan, Lijun J Nanobiotechnology Research BACKGROUND: Efficient and topical delivery of drugs is essential for maximized efficacy and minimized toxicity. In this study, we aimed to design an exosome-based drug delivery platform endowed with the ability of escaping from phagocytosis at non-target organs and controllably releasing drugs at targeted location. RESULTS: The swtichable stealth coat CP05-TK-mPEG was synthesized and anchored onto exosomes through the interaction between peptide CP05 and exosomal surface marker CD63. Chlorin e6 (Ce6) was loaded into exosomes by direct incubation. Controllable removal of PEG could be achieved by breaking thioketal (TK) through reactive oxygen species (ROS), which was produced by Ce6 under ultrasound irradiation. The whole platform was called SmartExo. The stealth effects were analyzed in RAW264.7 cells and C57BL/6 mice via tracing the exosomes. To confirm the efficacy of the engineered smart exosomes, Bone morphogenetic protein 7 (Bmp7) mRNA was encapsulated into exosomes by transfection of overexpressing plasmid, followed by stealth coating, with the exosomes designated as SmartExo@Bmp7. Therapeutic advantages of SmartExo@Bmp7 were proved by targeted delivering Bmp7 mRNA to omental adipose tissue (OAT) of obese C57BL/6 mice for browning induction. SmartExo platform was successfully constructed without changing the basic characteristics of exosomes. The engineered exosomes effectively escaped from the phagocytosis by RAW264.7 and non-target organs. In addition, the SmartExo could be uptaken locally on-demand by ultrasound mediated removal of the stealth coat. Compared with control exosomes, SmartExo@Bmp7 effectively delivered Bmp7 mRNA into OAT upon ultrasound irradiation, and induced OAT browning, as evidenced by the histology of OAT and increased expression of uncoupling protein 1 (Ucp1). CONCLUSIONS: The proposed SmartExo-based delivery platform, which minimizes side effects and maximizing drug efficacy, offers a novel safe and efficient approach for targeted drug delivery. As a proof, the SmartExo@Bmp7 induced local white adipose tissue browning, and it would be a promising strategy for anti-obesity therapy. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-01145-3. BioMed Central 2021-12-04 /pmc/articles/PMC8645082/ /pubmed/34863187 http://dx.doi.org/10.1186/s12951-021-01145-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Guo, Yitong
Wan, Zhuo
Zhao, Ping
Wei, Mengying
Liu, Yunnan
Bu, Te
Sun, Wenqi
Li, Zhelong
Yuan, Lijun
Ultrasound triggered topical delivery of Bmp7 mRNA for white fat browning induction via engineered smart exosomes
title Ultrasound triggered topical delivery of Bmp7 mRNA for white fat browning induction via engineered smart exosomes
title_full Ultrasound triggered topical delivery of Bmp7 mRNA for white fat browning induction via engineered smart exosomes
title_fullStr Ultrasound triggered topical delivery of Bmp7 mRNA for white fat browning induction via engineered smart exosomes
title_full_unstemmed Ultrasound triggered topical delivery of Bmp7 mRNA for white fat browning induction via engineered smart exosomes
title_short Ultrasound triggered topical delivery of Bmp7 mRNA for white fat browning induction via engineered smart exosomes
title_sort ultrasound triggered topical delivery of bmp7 mrna for white fat browning induction via engineered smart exosomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645082/
https://www.ncbi.nlm.nih.gov/pubmed/34863187
http://dx.doi.org/10.1186/s12951-021-01145-3
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