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Analyzing autophagosomes and mitophagosomes in the mouse brain using electron microscopy.
Duan, Kaizheng; Petralia, Ronald S; Wang, Ya-Xian; Li, Zheng.
Afiliação
  • Duan K; Section on Synapse Development Plasticity, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA.
  • Petralia RS; Advanced Imaging Core, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA.
  • Wang YX; Advanced Imaging Core, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA.
  • Li Z; Section on Synapse Development Plasticity, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA.
STAR Protoc ; 3(1): 101154, 2022 03 18.
Article em En | MEDLINE | ID: mdl-35169716
ABSTRACT
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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mitofagia / Autofagossomos Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mitofagia / Autofagossomos Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article