Evidence map›Paper›PMID 26617489›Full record

ArticleFrontiers in cellular neuroscience2015

Force Generation by Molecular-Motor-Powered Microtubule Bundles; Implications for Neuronal Polarization and Growth.

Maximilian Jakobs, Kristian Franze, Assaf Zemel

Abstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. The role of mechanics in axonal stability and development.Seminars in cell & developmental biology · 2023
    Review
  3. Article
  4. Mathematical models of neuronal growth.Biomechanics and modeling in mechanobiology · 2022
    Review
  5. Article
  6. Manipulation of Axonal Outgrowth via Exogenous Low Forces.International journal of molecular sciences · 2020
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. An Integrated Cytoskeletal Model of Neurite Outgrowth.Frontiers in cellular neuroscience · 2018
    Review
  13. Physical Biology of Axonal Damage.Frontiers in cellular neuroscience · 2018
    Article
  14. Article
  15. Modeling molecular mechanisms in the axon.Computational mechanics · 2017
    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

3 authors.

Maximilian JakobsDepartment of Physiology, Development and Neuroscience, University of Cambridge Cambridge, UK ; Bonn Cologne Graduate School of Physics and Astronomy, University of Cologne Cologne, Germany.
Kristian FranzeDepartment of Physiology, Development and Neuroscience, University of Cambridge Cambridge, UK.
Assaf ZemelInstitute of Dental Sciences and Fritz Haber Research Center for Molecular Dynamics, Hebrew University of Jerusalem Jerusalem, Israel.

Funding

Medical Research Council G1100312
6 · The paper itself

Abstract

The heavily cross-linked microtubule (MT) bundles found in neuronal processes play a central role in the initiation, growth and maturation of axons and dendrites; however, a quantitative understanding of their mechanical function is still lacking. We here developed computer simulations to investigate the dynamics of force generation in 1D bundles of MTs that are cross-linked and powered by molecular motors. The motion of filaments and the forces they exert are investigated as a function of the motor type (unipolar or bipolar), MT density and length, applied load, and motor connectivity. We demonstrate that only unipolar motors (e.g., kinesin-1) can provide the driving force for bundle expansion, while bipolar motors (e.g., kinesin-5) oppose it. The force generation capacity of the bundles is shown to depend sharply on the fraction of unipolar motors due to a percolation transition that must occur in the bundle. Scaling laws between bundle length, force, MT length and motor fraction are presented. In addition, we investigate the dynamics of growth in the presence of a constant influx of MTs. Beyond a short equilibration period, the bundles grow linearly in time. In this growth regime, the bundle extends as one mass forward with most filaments sliding with the growth velocity. The growth velocity is shown to be dictated by the inward flux of MTs, to inversely scale with the load and to be independent of the free velocity of the motors. These findings provide important molecular-level insights into the mechanical function of the MT cytoskeleton in normal axon growth and regeneration after injury.

Indexed as

axon outgrowthforce generationmicrotubulesmolecular motorsneuronal polarization

Identifiers

PMID26617489
PMCPMC4639704

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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.