Your browser doesn't support javascript.
loading
Labeling and measuring stressed mitochondria using a PINK1-based ratiometric fluorescent sensor.
Uesugi, Rie; Ishii, Shunsuke; Matsuura, Akira; Itakura, Eisuke.
Afiliação
  • Uesugi R; Department of Biology, Graduate School of Science and Engineering, Chiba University, Chiba, Japan.
  • Ishii S; Department of Biology, Graduate School of Science and Engineering, Chiba University, Chiba, Japan.
  • Matsuura A; Department of Biology, Graduate School of Science, Chiba University, Chiba, Japan.
  • Itakura E; Department of Biology, Graduate School of Science, Chiba University, Chiba, Japan. Electronic address: eitakura@chiba-u.jp.
J Biol Chem ; 297(5): 101279, 2021 11.
Article em En | MEDLINE | ID: mdl-34624312
ABSTRACT
Mitochondria are essential organelles that carry out a number of pivotal metabolic processes and maintain cellular homeostasis. Mitochondrial dysfunction caused by various stresses is associated with many diseases such as type 2 diabetes, obesity, cancer, heart failure, neurodegenerative disorders, and aging. Therefore, it is important to understand the stimuli that induce mitochondrial stress. However, broad analysis of mitochondrial stress has not been carried out to date. Here, we present a set of fluorescent tools, called mito-Pain (mitochondrial PINK1 accumulation index), which enable the labeling of stressed mitochondria. Mito-Pain uses PTEN-induced putative kinase 1 (PINK1) stabilization on mitochondria and quantifies mitochondrial stress levels by comparison with PINK1-GFP, which is stabilized under mitochondrial stress, and RFP-Omp25, which is constitutively localized on mitochondria. To identify compounds that induce mitochondrial stress, we screened a library of 3374 compounds using mito-Pain and identified 57 compounds as mitochondrial stress inducers. Furthermore, we classified each compound into several categories based on mitochondrial response depolarization, mitochondrial morphology, or Parkin recruitment. Parkin recruitment to mitochondria was often associated with mitochondrial depolarization and aggregation, suggesting that Parkin is recruited to heavily damaged mitochondria. In addition, many of the compounds led to various mitochondrial morphological changes, including fragmentation, aggregation, elongation, and swelling, with or without Parkin recruitment or mitochondrial depolarization. We also found that several compounds induced an ectopic response of Parkin, leading to the formation of cytosolic puncta dependent on PINK1. Thus, mito-Pain enables the detection of stressed mitochondria under a wide variety of conditions and provides insights into mitochondrial quality control systems.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Quinases / Estresse Fisiológico / Proteínas Mitocondriais / Bibliotecas de Moléculas Pequenas / Fluorescência / Corantes Fluorescentes / Mitocôndrias Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Quinases / Estresse Fisiológico / Proteínas Mitocondriais / Bibliotecas de Moléculas Pequenas / Fluorescência / Corantes Fluorescentes / Mitocôndrias Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article