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.

Highlights

  • Size, and distribution in response to various stimuli

  • Development of a novel fluorescent sensor for quantification of mitochondrial stress To quantify mitochondrial stress, we generated a plasmidbased ratiometric fluorescent sensor constructed with PTEN-induced putative kinase 1 (PINK1)-GFP, which is stabilized on mitochondria in a stressdependent manner

  • PINK1-GFP was linked with the T2A “self-cleaving” peptide sequence [29, 30] and fused with RFP and the transmembrane domain (TMD) of Omp25 [31], which is a tail-anchored protein that is inserted into the outer mitochondrial membrane (OMM) in a stress-independent manner to compensate for its expression level

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Summary

RESEARCH ARTICLE

Labeling and measuring stressed mitochondria using a PINK1-based ratiometric fluorescent sensor.

Edited by Ursula Jakob
Mitochondrial stress sensor
Results
Elongation Fragmentation Elongation Elongation
Ua Ub Ua Ub Ub Ub Ub
Discussion
Cell culture
Generation of stable cell lines by lentiviral and retroviral infection
Immunocytochemistry and fluorescence microscopy
Flow cytometry
Compound screening
Full Text
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