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Analyzing autophagosomes and mitophagosomes in the mouse brain using electron microscopy

Electron microscopy (EM) is considered the gold standard for studying macroautophagy and mitophagy, essential cellular processes for brain health. Here, we present a protocol using EM to analyze autophagosomes and mitophagosomes in the mouse amygdala. We describe the preparation of brain sections, f...

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Detalles Bibliográficos
Autores principales: Duan, Kaizheng, Petralia, Ronald S., Wang, Ya-Xian, Li, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8829798/
https://www.ncbi.nlm.nih.gov/pubmed/35169716
http://dx.doi.org/10.1016/j.xpro.2022.101154
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author Duan, Kaizheng
Petralia, Ronald S.
Wang, Ya-Xian
Li, Zheng
author_facet Duan, Kaizheng
Petralia, Ronald S.
Wang, Ya-Xian
Li, Zheng
author_sort Duan, Kaizheng
collection PubMed
description Electron microscopy (EM) is considered the gold standard for studying macroautophagy and mitophagy, essential cellular processes for brain health. Here, we present a protocol using EM to analyze autophagosomes and mitophagosomes in the mouse amygdala. We describe the preparation of brain sections, followed by staining and EM imaging. We then detail the steps to identify and analyze autophagosome-like and mitophagosome-like structures. This protocol can be easily adapted to analyze autophagosomes and mitophagosomes in other mouse brain regions. For complete details on the use and execution of this protocol, please refer to Duan et al. (2021).
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spelling pubmed-88297982022-02-14 Analyzing autophagosomes and mitophagosomes in the mouse brain using electron microscopy Duan, Kaizheng Petralia, Ronald S. Wang, Ya-Xian Li, Zheng STAR Protoc Protocol Electron microscopy (EM) is considered the gold standard for studying macroautophagy and mitophagy, essential cellular processes for brain health. Here, we present a protocol using EM to analyze autophagosomes and mitophagosomes in the mouse amygdala. We describe the preparation of brain sections, followed by staining and EM imaging. We then detail the steps to identify and analyze autophagosome-like and mitophagosome-like structures. This protocol can be easily adapted to analyze autophagosomes and mitophagosomes in other mouse brain regions. For complete details on the use and execution of this protocol, please refer to Duan et al. (2021). Elsevier 2022-02-03 /pmc/articles/PMC8829798/ /pubmed/35169716 http://dx.doi.org/10.1016/j.xpro.2022.101154 Text en © 2022. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Duan, Kaizheng
Petralia, Ronald S.
Wang, Ya-Xian
Li, Zheng
Analyzing autophagosomes and mitophagosomes in the mouse brain using electron microscopy
title Analyzing autophagosomes and mitophagosomes in the mouse brain using electron microscopy
title_full Analyzing autophagosomes and mitophagosomes in the mouse brain using electron microscopy
title_fullStr Analyzing autophagosomes and mitophagosomes in the mouse brain using electron microscopy
title_full_unstemmed Analyzing autophagosomes and mitophagosomes in the mouse brain using electron microscopy
title_short Analyzing autophagosomes and mitophagosomes in the mouse brain using electron microscopy
title_sort analyzing autophagosomes and mitophagosomes in the mouse brain using electron microscopy
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8829798/
https://www.ncbi.nlm.nih.gov/pubmed/35169716
http://dx.doi.org/10.1016/j.xpro.2022.101154
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