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Development of microglia-targeting adeno-associated viral vectors as tools to study microglial behavior in vivo

Here we describe the microglia-targeting adeno-associated viral (AAV) vectors containing a 1.7-kb putative promoter region of microglia/macrophage-specific ionized calcium-binding adaptor molecule 1 (Iba1), along with repeated miRNA target sites for microRNA (miR)-9 and miR-129-2-3p. The 1.7-kb geno...

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Autores principales: Okada, Yukihiro, Hosoi, Nobutake, Matsuzaki, Yasunori, Fukai, Yuuki, Hiraga, Akito, Nakai, Junichi, Nitta, Keisuke, Shinohara, Yoichiro, Konno, Ayumu, Hirai, Hirokazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652230/
https://www.ncbi.nlm.nih.gov/pubmed/36369525
http://dx.doi.org/10.1038/s42003-022-04200-3
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author Okada, Yukihiro
Hosoi, Nobutake
Matsuzaki, Yasunori
Fukai, Yuuki
Hiraga, Akito
Nakai, Junichi
Nitta, Keisuke
Shinohara, Yoichiro
Konno, Ayumu
Hirai, Hirokazu
author_facet Okada, Yukihiro
Hosoi, Nobutake
Matsuzaki, Yasunori
Fukai, Yuuki
Hiraga, Akito
Nakai, Junichi
Nitta, Keisuke
Shinohara, Yoichiro
Konno, Ayumu
Hirai, Hirokazu
author_sort Okada, Yukihiro
collection PubMed
description Here we describe the microglia-targeting adeno-associated viral (AAV) vectors containing a 1.7-kb putative promoter region of microglia/macrophage-specific ionized calcium-binding adaptor molecule 1 (Iba1), along with repeated miRNA target sites for microRNA (miR)-9 and miR-129-2-3p. The 1.7-kb genomic sequence upstream of the start codon in exon 1 of the Iba1 (Aif1) gene, functions as microglia preferential promoter in the striatum and cerebellum. Furthermore, ectopic transgene expression in non-microglial cells is markedly suppressed upon adding two sets of 4-repeated miRNA target sites for miR-9 and miR-129-2-3p, which are expressed exclusively in non-microglial cells and sponged AAV-derived mRNAs. Our vectors transduced ramified microglia in healthy tissues and reactive microglia in lipopolysaccharide-treated mice and a mouse model of neurodegenerative disease. Moreover, live fluorescent imaging allowed the monitoring of microglial motility and intracellular Ca(2+) mobilization. Thus, microglia-targeting AAV vectors are valuable for studying microglial pathophysiology and therapies, particularly in the striatum and cerebellum.
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spelling pubmed-96522302022-11-15 Development of microglia-targeting adeno-associated viral vectors as tools to study microglial behavior in vivo Okada, Yukihiro Hosoi, Nobutake Matsuzaki, Yasunori Fukai, Yuuki Hiraga, Akito Nakai, Junichi Nitta, Keisuke Shinohara, Yoichiro Konno, Ayumu Hirai, Hirokazu Commun Biol Article Here we describe the microglia-targeting adeno-associated viral (AAV) vectors containing a 1.7-kb putative promoter region of microglia/macrophage-specific ionized calcium-binding adaptor molecule 1 (Iba1), along with repeated miRNA target sites for microRNA (miR)-9 and miR-129-2-3p. The 1.7-kb genomic sequence upstream of the start codon in exon 1 of the Iba1 (Aif1) gene, functions as microglia preferential promoter in the striatum and cerebellum. Furthermore, ectopic transgene expression in non-microglial cells is markedly suppressed upon adding two sets of 4-repeated miRNA target sites for miR-9 and miR-129-2-3p, which are expressed exclusively in non-microglial cells and sponged AAV-derived mRNAs. Our vectors transduced ramified microglia in healthy tissues and reactive microglia in lipopolysaccharide-treated mice and a mouse model of neurodegenerative disease. Moreover, live fluorescent imaging allowed the monitoring of microglial motility and intracellular Ca(2+) mobilization. Thus, microglia-targeting AAV vectors are valuable for studying microglial pathophysiology and therapies, particularly in the striatum and cerebellum. Nature Publishing Group UK 2022-11-11 /pmc/articles/PMC9652230/ /pubmed/36369525 http://dx.doi.org/10.1038/s42003-022-04200-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Okada, Yukihiro
Hosoi, Nobutake
Matsuzaki, Yasunori
Fukai, Yuuki
Hiraga, Akito
Nakai, Junichi
Nitta, Keisuke
Shinohara, Yoichiro
Konno, Ayumu
Hirai, Hirokazu
Development of microglia-targeting adeno-associated viral vectors as tools to study microglial behavior in vivo
title Development of microglia-targeting adeno-associated viral vectors as tools to study microglial behavior in vivo
title_full Development of microglia-targeting adeno-associated viral vectors as tools to study microglial behavior in vivo
title_fullStr Development of microglia-targeting adeno-associated viral vectors as tools to study microglial behavior in vivo
title_full_unstemmed Development of microglia-targeting adeno-associated viral vectors as tools to study microglial behavior in vivo
title_short Development of microglia-targeting adeno-associated viral vectors as tools to study microglial behavior in vivo
title_sort development of microglia-targeting adeno-associated viral vectors as tools to study microglial behavior in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9652230/
https://www.ncbi.nlm.nih.gov/pubmed/36369525
http://dx.doi.org/10.1038/s42003-022-04200-3
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