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Axonal transport of Frizzled5 by Alcadein α-containing vesicles is associated with kinesin-1

Alcadein α (Alcα) and amyloid-β protein precursor (APP) are cargo receptors that associate vesicles with kinesin-1. These vesicles, which contain either Alcα or APP, transport various proteins/cargo molecules into axon nerve terminals. Here, we analyzed immune-isolated Alcα- and APP-containing vesic...

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Autores principales: Shiraki, Yuzuha, Mitsuma, Monet, Takada, Ritsuko, Hata, Saori, Kitamura, Akira, Takada, Shinji, Kinjo, Masataka, Taru, Hidenori, Müller, Ulrike C., Yamamoto, Tohru, Sobu, Yuriko, Suzuki, Toshiharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10559311/
https://www.ncbi.nlm.nih.gov/pubmed/37585286
http://dx.doi.org/10.1091/mbc.E22-10-0495
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author Shiraki, Yuzuha
Mitsuma, Monet
Takada, Ritsuko
Hata, Saori
Kitamura, Akira
Takada, Shinji
Kinjo, Masataka
Taru, Hidenori
Müller, Ulrike C.
Yamamoto, Tohru
Sobu, Yuriko
Suzuki, Toshiharu
author_facet Shiraki, Yuzuha
Mitsuma, Monet
Takada, Ritsuko
Hata, Saori
Kitamura, Akira
Takada, Shinji
Kinjo, Masataka
Taru, Hidenori
Müller, Ulrike C.
Yamamoto, Tohru
Sobu, Yuriko
Suzuki, Toshiharu
author_sort Shiraki, Yuzuha
collection PubMed
description Alcadein α (Alcα) and amyloid-β protein precursor (APP) are cargo receptors that associate vesicles with kinesin-1. These vesicles, which contain either Alcα or APP, transport various proteins/cargo molecules into axon nerve terminals. Here, we analyzed immune-isolated Alcα- and APP-containing vesicles of adult mouse brains with LC–MS/MS and identified proteins present in vesicles that contained either Alcα or APP. Among these proteins, Frizzled-5 (Fzd5), a Wnt receptor, was detected mainly in Alcα vesicles. Although colocalization ratios of Fzd5 with Alcα are low in the neurites of differentiating neurons by a low expression of Fzd5 in embryonic brains, the suppression of Alcα expression decreased the localization of Fzd5 in neurites of primary cultured neurons. Furthermore, Fzd5-EGFP expressed in primary cultured neurons was preferentially transported in axons with the transport velocities of Alcα vesicles. In synaptosomal fractions of adult-mice brains that express higher levels of Fzd5, the amount of Fzd5 and the phosphorylation level of calcium/calmodulin-dependent protein kinase-II were reduced in the Alcα-deficient mice. These results suggest that reduced transport of Fzd5 by Alcα-containing vesicles associated with kinesin-1 in axon terminals may impair the response to Wnt ligands in the noncanonical Ca(2+)-dependent signal transduction pathway at nerve terminals of mature neurons.
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spelling pubmed-105593112023-12-06 Axonal transport of Frizzled5 by Alcadein α-containing vesicles is associated with kinesin-1 Shiraki, Yuzuha Mitsuma, Monet Takada, Ritsuko Hata, Saori Kitamura, Akira Takada, Shinji Kinjo, Masataka Taru, Hidenori Müller, Ulrike C. Yamamoto, Tohru Sobu, Yuriko Suzuki, Toshiharu Mol Biol Cell Articles Alcadein α (Alcα) and amyloid-β protein precursor (APP) are cargo receptors that associate vesicles with kinesin-1. These vesicles, which contain either Alcα or APP, transport various proteins/cargo molecules into axon nerve terminals. Here, we analyzed immune-isolated Alcα- and APP-containing vesicles of adult mouse brains with LC–MS/MS and identified proteins present in vesicles that contained either Alcα or APP. Among these proteins, Frizzled-5 (Fzd5), a Wnt receptor, was detected mainly in Alcα vesicles. Although colocalization ratios of Fzd5 with Alcα are low in the neurites of differentiating neurons by a low expression of Fzd5 in embryonic brains, the suppression of Alcα expression decreased the localization of Fzd5 in neurites of primary cultured neurons. Furthermore, Fzd5-EGFP expressed in primary cultured neurons was preferentially transported in axons with the transport velocities of Alcα vesicles. In synaptosomal fractions of adult-mice brains that express higher levels of Fzd5, the amount of Fzd5 and the phosphorylation level of calcium/calmodulin-dependent protein kinase-II were reduced in the Alcα-deficient mice. These results suggest that reduced transport of Fzd5 by Alcα-containing vesicles associated with kinesin-1 in axon terminals may impair the response to Wnt ligands in the noncanonical Ca(2+)-dependent signal transduction pathway at nerve terminals of mature neurons. The American Society for Cell Biology 2023-09-21 /pmc/articles/PMC10559311/ /pubmed/37585286 http://dx.doi.org/10.1091/mbc.E22-10-0495 Text en © 2023 Shiraki et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial-Share Alike 4.0 International Creative Commons License.
spellingShingle Articles
Shiraki, Yuzuha
Mitsuma, Monet
Takada, Ritsuko
Hata, Saori
Kitamura, Akira
Takada, Shinji
Kinjo, Masataka
Taru, Hidenori
Müller, Ulrike C.
Yamamoto, Tohru
Sobu, Yuriko
Suzuki, Toshiharu
Axonal transport of Frizzled5 by Alcadein α-containing vesicles is associated with kinesin-1
title Axonal transport of Frizzled5 by Alcadein α-containing vesicles is associated with kinesin-1
title_full Axonal transport of Frizzled5 by Alcadein α-containing vesicles is associated with kinesin-1
title_fullStr Axonal transport of Frizzled5 by Alcadein α-containing vesicles is associated with kinesin-1
title_full_unstemmed Axonal transport of Frizzled5 by Alcadein α-containing vesicles is associated with kinesin-1
title_short Axonal transport of Frizzled5 by Alcadein α-containing vesicles is associated with kinesin-1
title_sort axonal transport of frizzled5 by alcadein α-containing vesicles is associated with kinesin-1
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10559311/
https://www.ncbi.nlm.nih.gov/pubmed/37585286
http://dx.doi.org/10.1091/mbc.E22-10-0495
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