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Gadolinium-based contrast agent accelerates the migration of astrocyte via integrin αvβ3 signaling pathway

Gadolinium (Gd)-based contrast agents (GBCAs) are chemicals injected intravenously during magnetic resonance imaging to enhance the diagnostic yield. Repeated use of GBCAs causes their deposition in the brain. Such deposition may affect various neuronal cells, including astrocytes. In this study, we...

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Autores principales: Ariyani, Winda, Miyazaki, Wataru, Tsushima, Yoshito, Koibuchi, Noriyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8990080/
https://www.ncbi.nlm.nih.gov/pubmed/35393504
http://dx.doi.org/10.1038/s41598-022-09882-7
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author Ariyani, Winda
Miyazaki, Wataru
Tsushima, Yoshito
Koibuchi, Noriyuki
author_facet Ariyani, Winda
Miyazaki, Wataru
Tsushima, Yoshito
Koibuchi, Noriyuki
author_sort Ariyani, Winda
collection PubMed
description Gadolinium (Gd)-based contrast agents (GBCAs) are chemicals injected intravenously during magnetic resonance imaging to enhance the diagnostic yield. Repeated use of GBCAs causes their deposition in the brain. Such deposition may affect various neuronal cells, including astrocytes. In this study, we examined the effect of GBCAs (Omniscan, Magnescope, Magnevist, and Gadovist) on astrocyte migration, which is critical for formation of neurons during development and maintaining brain homeostasis. All GBCAs increased cell migration and adhesion with increased actin remodelling. Knockdown of integrin αvβ3 by RNAi or exposure to integrin αvβ3 inhibitor reduced astrocyte migration. GBCAs increased phosphorylation of downstream factors of αvβ3, such as FAK, ERK1/2, and Akt. The phosphorylation of all these factors were reduced by RNAi or integrin αvβ3 inhibitor. GBCAs also increased the phosphorylation of their downstream factor, Rac1/cdc42, belonging to the RhoGTPases family. Coexposure to the selective RhoGTPases inhibitors, decreased the effects of GBCAs on cell migration. These findings indicate that GBCAs exert their action via integrin αvβ3 to activate the signaling pathway, resulting in increased astrocyte migration. Thus, the findings of the study suggest that it is important to avoid the repeated use of GBCAs to prevent adverse side effects in the brain, particularly during development.
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spelling pubmed-89900802022-04-11 Gadolinium-based contrast agent accelerates the migration of astrocyte via integrin αvβ3 signaling pathway Ariyani, Winda Miyazaki, Wataru Tsushima, Yoshito Koibuchi, Noriyuki Sci Rep Article Gadolinium (Gd)-based contrast agents (GBCAs) are chemicals injected intravenously during magnetic resonance imaging to enhance the diagnostic yield. Repeated use of GBCAs causes their deposition in the brain. Such deposition may affect various neuronal cells, including astrocytes. In this study, we examined the effect of GBCAs (Omniscan, Magnescope, Magnevist, and Gadovist) on astrocyte migration, which is critical for formation of neurons during development and maintaining brain homeostasis. All GBCAs increased cell migration and adhesion with increased actin remodelling. Knockdown of integrin αvβ3 by RNAi or exposure to integrin αvβ3 inhibitor reduced astrocyte migration. GBCAs increased phosphorylation of downstream factors of αvβ3, such as FAK, ERK1/2, and Akt. The phosphorylation of all these factors were reduced by RNAi or integrin αvβ3 inhibitor. GBCAs also increased the phosphorylation of their downstream factor, Rac1/cdc42, belonging to the RhoGTPases family. Coexposure to the selective RhoGTPases inhibitors, decreased the effects of GBCAs on cell migration. These findings indicate that GBCAs exert their action via integrin αvβ3 to activate the signaling pathway, resulting in increased astrocyte migration. Thus, the findings of the study suggest that it is important to avoid the repeated use of GBCAs to prevent adverse side effects in the brain, particularly during development. Nature Publishing Group UK 2022-04-07 /pmc/articles/PMC8990080/ /pubmed/35393504 http://dx.doi.org/10.1038/s41598-022-09882-7 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 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/) .
spellingShingle Article
Ariyani, Winda
Miyazaki, Wataru
Tsushima, Yoshito
Koibuchi, Noriyuki
Gadolinium-based contrast agent accelerates the migration of astrocyte via integrin αvβ3 signaling pathway
title Gadolinium-based contrast agent accelerates the migration of astrocyte via integrin αvβ3 signaling pathway
title_full Gadolinium-based contrast agent accelerates the migration of astrocyte via integrin αvβ3 signaling pathway
title_fullStr Gadolinium-based contrast agent accelerates the migration of astrocyte via integrin αvβ3 signaling pathway
title_full_unstemmed Gadolinium-based contrast agent accelerates the migration of astrocyte via integrin αvβ3 signaling pathway
title_short Gadolinium-based contrast agent accelerates the migration of astrocyte via integrin αvβ3 signaling pathway
title_sort gadolinium-based contrast agent accelerates the migration of astrocyte via integrin αvβ3 signaling pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8990080/
https://www.ncbi.nlm.nih.gov/pubmed/35393504
http://dx.doi.org/10.1038/s41598-022-09882-7
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