A new method for quantifying mitochondrial axonal transport

ABSTRACT Axonal transport of mitochondria is critical for neuronal survival and function. Automatically quantifying and analyzing mitochondrial movement in a large quantity remain challenging. Here, we report an efficient method for imaging and quantifying axonal mitochondrial transport using microf...

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Main Authors: Mengmeng Chen, Yang Li, Mengxue Yang, Xiaoping Chen, Yemeng Chen, Fan Yang, Sheng Lu, Shengyu Yao, Timothy Zhou, Jianghong Liu, Li Zhu, Sidan Du, Jane Y. Wu
Format: Article
Language:English
Published: Oxford University Press 2016-05-01
Series:Protein & Cell
Subjects:
Online Access:http://link.springer.com/article/10.1007/s13238-016-0268-3
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author Mengmeng Chen
Yang Li
Mengxue Yang
Xiaoping Chen
Yemeng Chen
Fan Yang
Sheng Lu
Shengyu Yao
Timothy Zhou
Jianghong Liu
Li Zhu
Sidan Du
Jane Y. Wu
author_facet Mengmeng Chen
Yang Li
Mengxue Yang
Xiaoping Chen
Yemeng Chen
Fan Yang
Sheng Lu
Shengyu Yao
Timothy Zhou
Jianghong Liu
Li Zhu
Sidan Du
Jane Y. Wu
author_sort Mengmeng Chen
collection DOAJ
description ABSTRACT Axonal transport of mitochondria is critical for neuronal survival and function. Automatically quantifying and analyzing mitochondrial movement in a large quantity remain challenging. Here, we report an efficient method for imaging and quantifying axonal mitochondrial transport using microfluidic-chamber-cultured neurons together with a newly developed analysis package named “MitoQuant”. This tool-kit consists of an automated program for tracking mitochondrial movement inside live neuronal axons and a transient-velocity analysis program for analyzing dynamic movement patterns of mitochondria. Using this method, we examined axonal mitochondrial movement both in cultured mammalian neurons and in motor neuron axons of Drosophila in vivo. In 3 different paradigms (temperature changes, drug treatment and genetic manipulation) that affect mitochondria, we have shown that this new method is highly efficient and sensitive for detecting changes in mitochondrial movement. The method significantly enhanced our ability to quantitatively analyze axonal mitochondrial movement and allowed us to detect dynamic changes in axonal mitochondrial transport that were not detected by traditional kymographic analyses.
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spelling doaj.art-64aa2bbe10a84a03b2d9fc6dd95174102023-09-02T09:53:01ZengOxford University PressProtein & Cell1674-800X1674-80182016-05-0171180481910.1007/s13238-016-0268-3A new method for quantifying mitochondrial axonal transportMengmeng Chen0Yang Li1Mengxue Yang2Xiaoping Chen3Yemeng Chen4Fan Yang5Sheng Lu6Shengyu Yao7Timothy Zhou8Jianghong Liu9Li Zhu10Sidan Du11Jane Y. Wu12University of Chinese Academy of SciencesSchool of Electronic Science & Engineering, Nanjing UniversityUniversity of Chinese Academy of SciencesDepartment of Neurology, Center for Genetic Medicine, Lurie Cancer Center, Northwestern University Feinberg School of MedicineSchool of Electronic Science & Engineering, Nanjing UniversitySchool of Electronic Science & Engineering, Nanjing UniversitySchool of Electronic Science & Engineering, Nanjing UniversityDepartment of Neurology, Center for Genetic Medicine, Lurie Cancer Center, Northwestern University Feinberg School of MedicineDepartment of Neurology, Center for Genetic Medicine, Lurie Cancer Center, Northwestern University Feinberg School of MedicineState Key Laboratory for Brain & Cognitive Science, Institute of Biophysics, Chinese Academy of SciencesState Key Laboratory for Brain & Cognitive Science, Institute of Biophysics, Chinese Academy of SciencesSchool of Electronic Science & Engineering, Nanjing UniversityState Key Laboratory for Brain & Cognitive Science, Institute of Biophysics, Chinese Academy of SciencesABSTRACT Axonal transport of mitochondria is critical for neuronal survival and function. Automatically quantifying and analyzing mitochondrial movement in a large quantity remain challenging. Here, we report an efficient method for imaging and quantifying axonal mitochondrial transport using microfluidic-chamber-cultured neurons together with a newly developed analysis package named “MitoQuant”. This tool-kit consists of an automated program for tracking mitochondrial movement inside live neuronal axons and a transient-velocity analysis program for analyzing dynamic movement patterns of mitochondria. Using this method, we examined axonal mitochondrial movement both in cultured mammalian neurons and in motor neuron axons of Drosophila in vivo. In 3 different paradigms (temperature changes, drug treatment and genetic manipulation) that affect mitochondria, we have shown that this new method is highly efficient and sensitive for detecting changes in mitochondrial movement. The method significantly enhanced our ability to quantitatively analyze axonal mitochondrial movement and allowed us to detect dynamic changes in axonal mitochondrial transport that were not detected by traditional kymographic analyses.http://link.springer.com/article/10.1007/s13238-016-0268-3mitochondrial transportimage processing and analysisFUS proteinopathy and mitochondrial transport defect
spellingShingle Mengmeng Chen
Yang Li
Mengxue Yang
Xiaoping Chen
Yemeng Chen
Fan Yang
Sheng Lu
Shengyu Yao
Timothy Zhou
Jianghong Liu
Li Zhu
Sidan Du
Jane Y. Wu
A new method for quantifying mitochondrial axonal transport
Protein & Cell
mitochondrial transport
image processing and analysis
FUS proteinopathy and mitochondrial transport defect
title A new method for quantifying mitochondrial axonal transport
title_full A new method for quantifying mitochondrial axonal transport
title_fullStr A new method for quantifying mitochondrial axonal transport
title_full_unstemmed A new method for quantifying mitochondrial axonal transport
title_short A new method for quantifying mitochondrial axonal transport
title_sort new method for quantifying mitochondrial axonal transport
topic mitochondrial transport
image processing and analysis
FUS proteinopathy and mitochondrial transport defect
url http://link.springer.com/article/10.1007/s13238-016-0268-3
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