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In Vitro and In Vivo Detection of Mitophagy in Human Cells, C. Elegans, and Mice.
Fang, Evandro F; Palikaras, Konstantinos; Sun, Nuo; Fivenson, Elayne M; Spangler, Ryan D; Kerr, Jesse S; Cordonnier, Stephanie A; Hou, Yujun; Dombi, Eszter; Kassahun, Henok; Tavernarakis, Nektarios; Poulton, Joanna; Nilsen, Hilde; Bohr, Vilhelm A.
Affiliation
  • Fang EF; Laboratory of Molecular Gerontology, National Institute on Aging, National Institutes of Health; Department of Clinical Molecular Biology, University of Oslo and Akershus University Hospital; evandrofeifang@yahoo.com; e.f.fang@medisin.uio.no.
  • Palikaras K; Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology - Hellas.
  • Sun N; Center for Molecular Medicine, National Heart Lung and Blood Institute, National Institutes of Health.
  • Fivenson EM; Laboratory of Molecular Gerontology, National Institute on Aging, National Institutes of Health.
  • Spangler RD; Laboratory of Neurosciences, National Institute on Aging, National Institutes of Health.
  • Kerr JS; Laboratory of Molecular Gerontology, National Institute on Aging, National Institutes of Health.
  • Cordonnier SA; Laboratory of Molecular Gerontology, National Institute on Aging, National Institutes of Health.
  • Hou Y; Laboratory of Molecular Gerontology, National Institute on Aging, National Institutes of Health.
  • Dombi E; Nuffield Department of Obstetrics and Gynaecology, University of Oxford.
  • Kassahun H; Department of Clinical Molecular Biology, University of Oslo and Akershus University Hospital.
  • Tavernarakis N; Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology - Hellas; Department of Basic Sciences, Faculty of Medicine, University of Crete.
  • Poulton J; Nuffield Department of Obstetrics and Gynaecology, University of Oxford.
  • Nilsen H; Department of Clinical Molecular Biology, University of Oslo and Akershus University Hospital.
  • Bohr VA; Laboratory of Molecular Gerontology, National Institute on Aging, National Institutes of Health; Danish Center for Healthy Aging, University of Copenhagen; BohrV@grc.nia.nih.gov.
J Vis Exp ; (129)2017 11 22.
Article in En | MEDLINE | ID: mdl-29286376
Mitochondria are the powerhouses of cells and produce cellular energy in the form of ATP. Mitochondrial dysfunction contributes to biological aging and a wide variety of disorders including metabolic diseases, premature aging syndromes, and neurodegenerative diseases such as Alzheimer's disease (AD) and Parkinson's disease (PD). Maintenance of mitochondrial health depends on mitochondrial biogenesis and the efficient clearance of dysfunctional mitochondria through mitophagy. Experimental methods to accurately detect autophagy/mitophagy, especially in animal models, have been challenging to develop. Recent progress towards the understanding of the molecular mechanisms of mitophagy has enabled the development of novel mitophagy detection techniques. Here, we introduce several versatile techniques to monitor mitophagy in human cells, Caenorhabditis elegans (e.g., Rosella and DCT-1/ LGG-1 strains), and mice (mt-Keima). A combination of these mitophagy detection techniques, including cross-species evaluation, will improve the accuracy of mitophagy measurements and lead to a better understanding of the role of mitophagy in health and disease.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Caenorhabditis elegans / Caenorhabditis elegans Proteins / Mitophagy / Mitochondria Type of study: Diagnostic_studies Limits: Animals / Female / Humans / Male Language: En Journal: J Vis Exp Year: 2017 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Caenorhabditis elegans / Caenorhabditis elegans Proteins / Mitophagy / Mitochondria Type of study: Diagnostic_studies Limits: Animals / Female / Humans / Male Language: En Journal: J Vis Exp Year: 2017 Document type: Article Country of publication: United States