Evidence map›Paper›PMID 31180320›Full record

ArticleeLife2019

Nanoresolution real-time 3D orbital tracking for studying mitochondrial trafficking in vertebrate axons in vivo.

Fabian Wehnekamp, Gabriela Plucińska, Rachel Thong, Thomas Misgeld, Don C Lamb

Abstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Real-Time Feedback-Driven Single-Particle Tracking: A Survey and Perspective.Small (Weinheim an der Bergstrasse, Germany) · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Pleiotropic Mitochondria: The Influence of Mitochondria on Neuronal Development and Disease.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Review
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Fabian Wehnekamp *Department of Chemistry, Center for Nano Science (CENS), Center for Integrated Protein Science (CIPSM) and Nanosystems Initiative München (NIM), Ludwig Maximilians-Universität München, Munich, Germany.
Gabriela Plucińska *Munich Cluster for Systems Neurology (SNergy), Center for Integrated Protein Science (CIPSM), German Center for Neurodegenerative Diseases (DZNE), Institute of Neuronal Cell Biology, Technische Universität München, Munich, Germany.
Rachel ThongMunich Cluster for Systems Neurology (SNergy), Center for Integrated Protein Science (CIPSM), German Center for Neurodegenerative Diseases (DZNE), Institute of Neuronal Cell Biology, Technische Universität München, Munich, Germany.
Thomas MisgeldMunich Cluster for Systems Neurology (SNergy), Center for Integrated Protein Science (CIPSM), German Center for Neurodegenerative Diseases (DZNE), Institute of Neuronal Cell Biology, Technische Universität München, Munich, Germany.ORCID 0000-0001-9875-6794
Don C LambDepartment of Chemistry, Center for Nano Science (CENS), Center for Integrated Protein Science (CIPSM) and Nanosystems Initiative München (NIM), Ludwig Maximilians-Universität München, Munich, Germany.ORCID 0000-0002-0232-1903

Funding

Deutsche Forschungsgemeinschaft Munich Cluster for Systems Neurology (SyNergy) EXC 2145Deutsche Forschungsgemeinschaft Priority Program SPP1710Deutsche Forschungsgemeinschaft research grants Mi 694/7Deutsche Forschungsgemeinschaft Research grants Mi 694/7+8Deutsche Forschungsgemeinschaft SFB1032 (Project B3)Deutsche Forschungsgemeinschaft SFB870 15 (Project A11)Fakultät für Chemie und Pharmazie, Ludwig-Maximilians-Universität München Center for NanoScience (CeNS) and the BioImaging Network (BIN)H2020 European Research Council ERC Grant Agreement n. 616791
6 · The paper itself

Abstract

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.

Indexed as

AnimalsAxonsBiological TransportCell TrackingImaging, Three-DimensionalLarvaMicroscopy, ConfocalMitochondriaNanotechnologySensory Receptor CellsVertebratesZebrafishfluorescencemitochondria traffickingmolecular biophysicsphysics of living systemssingle particle trackingstructural biologyzebrafish

Identifiers

PMID31180320
PMCPMC6579510

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.