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Techniques to Investigate Mitochondrial Function in Neurons

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Cover of 'Techniques to Investigate Mitochondrial Function in Neurons'

Table of Contents

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    Book Overview
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    Chapter 1 Three-Dimensional Reconstruction of Neuronal Mitochondria by Electron Tomography
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    Chapter 2 Measuring Mitochondrial Shape with ImageJ
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    Chapter 3 Live Imaging Mitochondrial Transport in Neurons
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    Chapter 4 Techniques to Investigate Bioenergetics of Mitochondria
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    Chapter 5 Respirometry in Neurons
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    Chapter 6 Measuring ATP in Axons with FRET
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    Chapter 7 Characterizing Metabolic States Using Fluorescence Lifetime Imaging Microscopy (FLIM) of NAD(P)H
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    Chapter 8 Techniques for Simultaneous Mitochondrial and Cytosolic Ca 2+ Imaging in Neurons
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    Chapter 9 Live Imaging of Mitochondrial ROS Production and Dynamic Redox Balance in Neurons
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    Chapter 10 Monitoring of Permeability Transition Pore Openings in Isolated Individual Brain Mitochondria
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    Chapter 11 Examination of Mitochondrial Ion Conductance by Patch Clamp in Intact Neurons and Mitochondrial Membrane Preparations
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    Chapter 12 Monitoring of Permeability Transition Pore Openings in Mitochondria of Cultured Neurons
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    Chapter 13 Protocols for Assessing Mitophagy in Neuronal Cell Lines and Primary Neurons
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    Chapter 14 Examining Mitochondrial Function at Synapses In Situ
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    Chapter 15 Proteomic Analysis of Neuronal Mitochondria
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    Chapter 16 Measuring Mitochondrial Pyruvate Oxidation
Attention for Chapter 13: Protocols for Assessing Mitophagy in Neuronal Cell Lines and Primary Neurons
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Chapter title
Protocols for Assessing Mitophagy in Neuronal Cell Lines and Primary Neurons
Chapter number 13
Book title
Techniques to Investigate Mitochondrial Function in Neurons
Published in
Neuromethods, January 2017
DOI 10.1007/978-1-4939-6890-9_13
Pubmed ID
Book ISBNs
978-1-4939-6888-6, 978-1-4939-6890-9, 978-1-4939-6888-6, 978-1-4939-6890-9
Authors

Ruben K. Dagda, Monica Rice, Dagda, Ruben K., Rice, Monica

Abstract

Mitochondria are organelles that regulate essential eukaryotic functions including generating energy, sequestering excess calcium, and modulating cell survival. In order for neurons to thrive, mitochondria have to be continuously replenished by maintaining autophagic-lysosomal mediated degradation of mitochondria (mitophagy) and mitochondrial biogenesis. While a plethora of image- and biochemical-based techniques have been developed for measuring autophagy (macroautophagy) in eukaryotic cells, the molecular toolbox for quantifying and assessing mitophagy in neurons continues to evolve. Compared to proliferating cells, quantifying mitophagy in neurons poses a technical challenge given that mitochondria are predominantly present in neurites (axons and dendrites) and are highly dynamic. In this chapter, we provide a brief overview on mitophagy and provide a list of validated fluorescence- and biochemistry-based techniques used for assessing mitophagy in neuronal cells and primary neurons. Secondly, we provide comprehensive guidelines for interpreting steady-state levels of mitophagy and mitophagic flux in neurons using modern fluorescence- and biochemistry-based techniques. Finally, we provide a comprehensive list of common pitfalls to avoid when assessing mitophagy and offer practical solutions to overcome technical issues.

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Mendeley readers

The data shown below were compiled from readership statistics for 25 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 25 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 4 16%
Student > Ph. D. Student 3 12%
Unspecified 2 8%
Student > Bachelor 2 8%
Student > Master 2 8%
Other 2 8%
Unknown 10 40%
Readers by discipline Count As %
Neuroscience 6 24%
Biochemistry, Genetics and Molecular Biology 4 16%
Unspecified 2 8%
Immunology and Microbiology 1 4%
Psychology 1 4%
Other 0 0%
Unknown 11 44%