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Targeted delivery to macrophages and dendritic cells by chemically modified mannose ligand-conjugated siRNA

Extrahepatic delivery of small interfering RNAs (siRNAs) may have applications in the development of novel therapeutic approaches. However, reports on such approaches are limited, and the scarcity of reports concerning the systemically targeted delivery of siRNAs with effective gene silencing activi...

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Autores principales: Uehara, Keiji, Harumoto, Toshimasa, Makino, Asana, Koda, Yasuo, Iwano, Junko, Suzuki, Yasuhiro, Tanigawa, Mari, Iwai, Hiroto, Asano, Kana, Kurihara, Kana, Hamaguchi, Akinori, Kodaira, Hiroshi, Atsumi, Toshiyuki, Yamada, Yoji, Tomizuka, Kazuma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122583/
https://www.ncbi.nlm.nih.gov/pubmed/35524566
http://dx.doi.org/10.1093/nar/gkac308
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author Uehara, Keiji
Harumoto, Toshimasa
Makino, Asana
Koda, Yasuo
Iwano, Junko
Suzuki, Yasuhiro
Tanigawa, Mari
Iwai, Hiroto
Asano, Kana
Kurihara, Kana
Hamaguchi, Akinori
Kodaira, Hiroshi
Atsumi, Toshiyuki
Yamada, Yoji
Tomizuka, Kazuma
author_facet Uehara, Keiji
Harumoto, Toshimasa
Makino, Asana
Koda, Yasuo
Iwano, Junko
Suzuki, Yasuhiro
Tanigawa, Mari
Iwai, Hiroto
Asano, Kana
Kurihara, Kana
Hamaguchi, Akinori
Kodaira, Hiroshi
Atsumi, Toshiyuki
Yamada, Yoji
Tomizuka, Kazuma
author_sort Uehara, Keiji
collection PubMed
description Extrahepatic delivery of small interfering RNAs (siRNAs) may have applications in the development of novel therapeutic approaches. However, reports on such approaches are limited, and the scarcity of reports concerning the systemically targeted delivery of siRNAs with effective gene silencing activity presents a challenge. We herein report for the first time the targeted delivery of CD206-targetable chemically modified mannose–siRNA (CMM–siRNA) conjugates to macrophages and dendritic cells (DCs). CMM–siRNA exhibited a strong binding ability to CD206 and selectively delivered contents to CD206-expressing macrophages and DCs. Furthermore, the conjugates demonstrated strong gene silencing ability with long-lasting effects and protein downregulation in CD206-expressing cells in vivo. These findings could broaden the use of siRNA technology, provide additional therapeutic opportunities, and establish a basis for further innovative approaches for the targeted delivery of siRNAs to not only macrophages and DCs but also other cell types.
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spelling pubmed-91225832022-05-23 Targeted delivery to macrophages and dendritic cells by chemically modified mannose ligand-conjugated siRNA Uehara, Keiji Harumoto, Toshimasa Makino, Asana Koda, Yasuo Iwano, Junko Suzuki, Yasuhiro Tanigawa, Mari Iwai, Hiroto Asano, Kana Kurihara, Kana Hamaguchi, Akinori Kodaira, Hiroshi Atsumi, Toshiyuki Yamada, Yoji Tomizuka, Kazuma Nucleic Acids Res Chemical Biology and Nucleic Acid Chemistry Extrahepatic delivery of small interfering RNAs (siRNAs) may have applications in the development of novel therapeutic approaches. However, reports on such approaches are limited, and the scarcity of reports concerning the systemically targeted delivery of siRNAs with effective gene silencing activity presents a challenge. We herein report for the first time the targeted delivery of CD206-targetable chemically modified mannose–siRNA (CMM–siRNA) conjugates to macrophages and dendritic cells (DCs). CMM–siRNA exhibited a strong binding ability to CD206 and selectively delivered contents to CD206-expressing macrophages and DCs. Furthermore, the conjugates demonstrated strong gene silencing ability with long-lasting effects and protein downregulation in CD206-expressing cells in vivo. These findings could broaden the use of siRNA technology, provide additional therapeutic opportunities, and establish a basis for further innovative approaches for the targeted delivery of siRNAs to not only macrophages and DCs but also other cell types. Oxford University Press 2022-05-07 /pmc/articles/PMC9122583/ /pubmed/35524566 http://dx.doi.org/10.1093/nar/gkac308 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemical Biology and Nucleic Acid Chemistry
Uehara, Keiji
Harumoto, Toshimasa
Makino, Asana
Koda, Yasuo
Iwano, Junko
Suzuki, Yasuhiro
Tanigawa, Mari
Iwai, Hiroto
Asano, Kana
Kurihara, Kana
Hamaguchi, Akinori
Kodaira, Hiroshi
Atsumi, Toshiyuki
Yamada, Yoji
Tomizuka, Kazuma
Targeted delivery to macrophages and dendritic cells by chemically modified mannose ligand-conjugated siRNA
title Targeted delivery to macrophages and dendritic cells by chemically modified mannose ligand-conjugated siRNA
title_full Targeted delivery to macrophages and dendritic cells by chemically modified mannose ligand-conjugated siRNA
title_fullStr Targeted delivery to macrophages and dendritic cells by chemically modified mannose ligand-conjugated siRNA
title_full_unstemmed Targeted delivery to macrophages and dendritic cells by chemically modified mannose ligand-conjugated siRNA
title_short Targeted delivery to macrophages and dendritic cells by chemically modified mannose ligand-conjugated siRNA
title_sort targeted delivery to macrophages and dendritic cells by chemically modified mannose ligand-conjugated sirna
topic Chemical Biology and Nucleic Acid Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122583/
https://www.ncbi.nlm.nih.gov/pubmed/35524566
http://dx.doi.org/10.1093/nar/gkac308
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