Evidence map›Paper›PMID 29079766›Full record

ArticleScientific reports2017

Coupled circumferential and axial tension driven by actin and myosin influences in vivo axon diameter.

Anthony Fan, Alireza Tofangchi, Mikhail Kandel, Gabriel Popescu, Taher Saif

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Review
  3. Schwann Cell Development and Myelination.Cold Spring Harbor perspectives in biology · 2024
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  5. Article
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  8. The role of mechanics in axonal stability and development.Seminars in cell & developmental biology · 2023
    Review
  9. Article
  10. Unraveling axonal mechanisms of traumatic brain injury.Acta neuropathologica communications · 2022
    Article
  11. Article
  12. Article
  13. The role of the membrane-associated periodic skeleton in axons.Cellular and molecular life sciences : CMLS · 2021
    Review
  14. Article
  15. Article
  16. Review
  17. Increased Susceptibility to Glaucomatous Damage in Microfibril Deficient Mice.Investigative ophthalmology & visual science · 2020
    Article
  18. Article
  19. Article
  20. 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 at 1 institution in 1 country.

Anthony FanDepartment of Mechanical Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Alireza TofangchiDepartment of Mechanical Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Mikhail KandelDepartment of Electrical and Computer Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA.ORCID 0000-0003-2124-7750
Gabriel PopescuDepartment of Electrical and Computer Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA.
Taher SaifDepartment of Mechanical Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA. saif@illinois.edu.
University of Illinois Urbana-Champaign · US

Funding

Mechanical Force and Neural RegenerationR01NS063405 · NINDS · UNIVERSITY OF MIAMI CORAL GABLES · PI CHIBA, AKIRA, JAKOBSSON, ERIC G · 2008 to 2011
$1.2M
NINDS NIH HHS R01 NS063405
6 · The paper itself

Abstract

It has long been known that neuronal axons are contractile. They actively maintain rest tension along the longitudinal direction both in vitro and in vivo. Here we show evidence that embryonic drosophila axons also actively maintain contractility/tension along the circumferential direction. We used confocal microscopy and spatial light interference microscopy to monitor axonal diameter along their length. We observed a decrease in diameter when microtubules are disrupted and an increase in diameter when actin filaments or myosin II are disrupted. Interestingly, active diameter reduction occurred consistently when axons were subjected to manipulations known to increase axial tension, suggesting that tension can be coupled in the axial and circumferential direction. This is further supported by the remarkably similar time constants for diameter reduction and rest tension increase of slackened axons. We infer that the actomyosin-driven circumferential contraction/hoop tension applies a squeezing force on the microtubule bundle of the axons. This hoop tension is balanced by the restoring force of the microtubule bundle. Therefore, axonal diameter increased when actin/myosin disrupting drugs relaxed the hoop tension and decreased when microtubule disrupting drug relaxed the restoring force. Circumferential tension thus can regulate axonal diameter and volume, as well as potentially microtubules alignment, inter-tubular spacing, and, by extension, axonal transport.

Indexed as

Stress, MechanicalActinsAnimalsAxonsBiomechanical PhenomenaDrosophila melanogasterKineticsMicrotubulesMyosinsActinsMyosins

Identifiers

PMID29079766
PMCPMC5660205
OpenAlexW2765516952

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.