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Mitophagy

Overview of attention for book
Cover of 'Mitophagy'

Table of Contents

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    Book Overview
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    Chapter 7 Induction of PINK1/Parkin-Mediated Mitophagy
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    Chapter 8 The Use of Correlative Light-Electron Microscopy (CLEM) to Study PINK1/Parkin-Mediated Mitophagy
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    Chapter 9 Monitoring Mitochondrial Changes by Alteration of the PINK1-Parkin Signaling in Drosophila
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    Chapter 10 Assessment of Mitophagy in iPS Cell-Derived Neurons
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    Chapter 11 Investigation of Yeast Mitophagy with Fluorescence Microscopy and Western Blotting
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    Chapter 12 MitoPho8Δ60 Assay as a Tool to Quantitatively Measure Mitophagy Activity
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    Chapter 13 Mitophagy in Yeast: A Screen of Mitophagy-Deficient Mutants
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    Chapter 14 Flow Cytometer Monitoring of Bnip3- and Bnip3L/Nix-Dependent Mitophagy
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    Chapter 15 Exploring MicroRNAs on NIX-Dependent Mitophagy
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    Chapter 16 Monitoring of Atg5-Independent Mitophagy
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    Chapter 17 Monitoring of Paternal Mitochondrial Degradation in Caenorhabditis elegans
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    Chapter 18 Monitoring Mitophagy During Aging in Caenorhabditis elegans
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    Chapter 19 Detection of Hypoxia-Induced and Iron Depletion-Induced Mitophagy in Mammalian Cells
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    Chapter 20 Immunocytochemical Monitoring of PINK1/Parkin-Mediated Mitophagy in Cultured Cells
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    Chapter 38 Short Overview
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    Chapter 39 Observation of Parkin-Mediated Mitophagy in Pancreatic β-Cells
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    Chapter 40 Monitoring of Iron Depletion-Induced Mitophagy in Pathogenic Yeast
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    Chapter 156 Dopaminergic Neuron-Specific Autophagy-Deficient Mice
Attention for Chapter 8: The Use of Correlative Light-Electron Microscopy (CLEM) to Study PINK1/Parkin-Mediated Mitophagy
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Chapter title
The Use of Correlative Light-Electron Microscopy (CLEM) to Study PINK1/Parkin-Mediated Mitophagy
Chapter number 8
Book title
Mitophagy
Published in
Methods in molecular biology, March 2017
DOI 10.1007/7651_2017_8
Pubmed ID
Book ISBNs
978-1-4939-7749-9, 978-1-4939-7750-5
Authors

Kishi-Itakura, Chieko, Buss, Folma, Chieko Kishi-Itakura, Folma Buss

Abstract

In this chapter we describe the use of correlative light-electron microscopy (CLEM) to study, in cultured cells, the turnover of damaged mitochondria by PINK1/Parkin-dependent mitophagy. CLEM combines the advantages of light microscopy, which allows to image and rapidly screen a large number of the cells, while electron microscopy provides high-resolution imaging of these selected cells and a detailed structural analysis of their cellular organelles. We describe in detail how to prepare the cell cultures for optimum preservation of their cellular ultrastructure for CLEM using the most suitable buffers, fixatives, and embedding resins. These protocols are applicable for detailed ultrastructural analysis in a wide variety of organisms and cells, ranging from prokaryotic bacteria to mammalian cells.

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Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 15 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 3 20%
Researcher 2 13%
Student > Ph. D. Student 2 13%
Unspecified 1 7%
Professor > Associate Professor 1 7%
Other 1 7%
Unknown 5 33%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 33%
Agricultural and Biological Sciences 3 20%
Unspecified 1 7%
Neuroscience 1 7%
Unknown 5 33%