Evidence map›Paper›PMID 36322761›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Nano-positioning and tubulin conformation contribute to axonal transport regulation of mitochondria along microtubules.

Valérie Van Steenbergen, Flavie Lavoie-Cardinal, Youcef Kazwiny, Marianna Decet, Tobie Martens, Patrik Verstreken, Werend Boesmans, Paul De Koninck, Pieter Vanden Berghe

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Mechano-energetic uncoupling in heart failure.Nature reviews. Cardiology · 2025
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  9. Low-Dose Non-Targeted Effects and Mitochondrial Control.International journal of molecular sciences · 2023
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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

9 authors at 4 institutions in 4 countries.

Valérie Van SteenbergenLaboratory for Enteric Neuroscience, Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, 3000, Belgium.
Flavie Lavoie-CardinalCERVO Brain Research Center, Université Laval, Québec, G1J 2G3, Canada.
Youcef KazwinyLaboratory for Enteric Neuroscience, Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, 3000, Belgium.
Marianna DecetLeuven Brain Institute, KU Leuven, Leuven, 3000, Belgium.
Tobie MartensLaboratory for Enteric Neuroscience, Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, 3000, Belgium.
Patrik VerstrekenLeuven Brain Institute, KU Leuven, Leuven, 3000, Belgium.
Werend BoesmansLaboratory for Enteric Neuroscience, Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, 3000, Belgium.
Paul De KoninckCERVO Brain Research Center, Université Laval, Québec, G1J 2G3, Canada.
Pieter Vanden BergheLaboratory for Enteric Neuroscience, Department of Chronic Diseases, Metabolism and Ageing, KU Leuven, Leuven, 3000, Belgium.
Hasselt University · BEKU Leuven · BEUniversity of Vermont · USVIB-KU Leuven Center for Brain & Disease Research · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Correct spatiotemporal distribution of organelles and vesicles is crucial for healthy cell functioning and is regulated by intracellular transport mechanisms. Controlled transport of bulky mitochondria is especially important in polarized cells such as neurons that rely on these organelles to locally produce energy and buffer calcium. Mitochondrial transport requires and depends on microtubules that fill much of the available axonal space. How mitochondrial transport is affected by their position within the microtubule bundles is not known. Here, we found that anterograde transport, driven by kinesin motors, is susceptible to the molecular conformation of tubulin in neurons both in vitro and in vivo. Anterograde velocities negatively correlate with the density of elongated tubulin dimers like guanosine triphosphate (GTP)-tubulin. The impact of the tubulin conformation depends primarily on where a mitochondrion is positioned, either within or at the rim of microtubule bundle. Increasing elongated tubulin levels lowers the number of motile anterograde mitochondria within the microtubule bundle and increases anterograde transport speed at the microtubule bundle rim. We demonstrate that the increased kinesin velocity and density on microtubules consisting of elongated dimers add to the increased mitochondrial dynamics. Our work indicates that the molecular conformation of tubulin contributes to the regulation of mitochondrial motility and as such to the local distribution of mitochondria along axons.

Indexed as

Axonal TransportTubulinAxonsKinesinsMicrotubulesMitochondriaMolecular ConformationKinesinsTubulinmicrotubulesmitochondrianeuronal axonSTEDtransport

Identifiers

PMID36322761
PMCPMC9659393
OpenAlexW4308145472

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.