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Nanoresolution real-time 3D orbital tracking for studying mitochondrial trafficking in vertebrate axons in vivo
We present the development and in vivo application of a feedback-based tracking microscope to follow individual mitochondria in sensory neurons of zebrafish larvae with nanometer precision and millisecond temporal resolution. By combining various technical improvements, we tracked individual mitocho...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6579510/ https://www.ncbi.nlm.nih.gov/pubmed/31180320 http://dx.doi.org/10.7554/eLife.46059 |
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author | Wehnekamp, Fabian Plucińska, Gabriela Thong, Rachel Misgeld, Thomas Lamb, Don C |
author_facet | Wehnekamp, Fabian Plucińska, Gabriela Thong, Rachel Misgeld, Thomas Lamb, Don C |
author_sort | Wehnekamp, Fabian |
collection | PubMed |
description | We present the development and in vivo application of a feedback-based tracking microscope to follow individual mitochondria in sensory neurons of zebrafish larvae with nanometer precision and millisecond temporal resolution. By combining various technical improvements, we tracked individual mitochondria with unprecedented spatiotemporal resolution over distances of >100 µm. Using these nanoscopic trajectory data, we discriminated five motional states: a fast and a slow directional motion state in both the anterograde and retrograde directions and a stationary state. The transition pattern revealed that, after a pause, mitochondria predominantly persist in the original direction of travel, while transient changes of direction often exhibited longer pauses. Moreover, mitochondria in the vicinity of a second, stationary mitochondria displayed an increased probability to pause. The capability of following and optically manipulating a single organelle with high spatiotemporal resolution in a living organism offers a new approach to elucidating their function in its complete physiological context. |
format | Online Article Text |
id | pubmed-6579510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-65795102019-06-19 Nanoresolution real-time 3D orbital tracking for studying mitochondrial trafficking in vertebrate axons in vivo Wehnekamp, Fabian Plucińska, Gabriela Thong, Rachel Misgeld, Thomas Lamb, Don C eLife Physics of Living Systems We present the development and in vivo application of a feedback-based tracking microscope to follow individual mitochondria in sensory neurons of zebrafish larvae with nanometer precision and millisecond temporal resolution. By combining various technical improvements, we tracked individual mitochondria with unprecedented spatiotemporal resolution over distances of >100 µm. Using these nanoscopic trajectory data, we discriminated five motional states: a fast and a slow directional motion state in both the anterograde and retrograde directions and a stationary state. The transition pattern revealed that, after a pause, mitochondria predominantly persist in the original direction of travel, while transient changes of direction often exhibited longer pauses. Moreover, mitochondria in the vicinity of a second, stationary mitochondria displayed an increased probability to pause. The capability of following and optically manipulating a single organelle with high spatiotemporal resolution in a living organism offers a new approach to elucidating their function in its complete physiological context. eLife Sciences Publications, Ltd 2019-06-10 /pmc/articles/PMC6579510/ /pubmed/31180320 http://dx.doi.org/10.7554/eLife.46059 Text en © 2019, Wehnekamp et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Physics of Living Systems Wehnekamp, Fabian Plucińska, Gabriela Thong, Rachel Misgeld, Thomas Lamb, Don C Nanoresolution real-time 3D orbital tracking for studying mitochondrial trafficking in vertebrate axons in vivo |
title | Nanoresolution real-time 3D orbital tracking for studying mitochondrial trafficking in vertebrate axons in vivo |
title_full | Nanoresolution real-time 3D orbital tracking for studying mitochondrial trafficking in vertebrate axons in vivo |
title_fullStr | Nanoresolution real-time 3D orbital tracking for studying mitochondrial trafficking in vertebrate axons in vivo |
title_full_unstemmed | Nanoresolution real-time 3D orbital tracking for studying mitochondrial trafficking in vertebrate axons in vivo |
title_short | Nanoresolution real-time 3D orbital tracking for studying mitochondrial trafficking in vertebrate axons in vivo |
title_sort | nanoresolution real-time 3d orbital tracking for studying mitochondrial trafficking in vertebrate axons in vivo |
topic | Physics of Living Systems |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6579510/ https://www.ncbi.nlm.nih.gov/pubmed/31180320 http://dx.doi.org/10.7554/eLife.46059 |
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