Evidence map›Paper›PMID 27796302›Full record

ArticleNature communications2016

Thick filament mechano-sensing is a calcium-independent regulatory mechanism in skeletal muscle.

L Fusi, E Brunello, Z Yan, M Irving

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
9.0field-weighted citation impact, top 2% 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

89 citing papers in PubMed, 127 citations in OpenAlex.

  1. Article
  2. Article
  3. Subsarcomeric regulation of thin and thick filaments in skeletal muscle myofibrils.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Consecutive SSCs increase the SSC effect in skinned rat muscle fibres.Pflugers Archiv : European journal of physiology · 2025
    Article
  9. The distinctive mechanical and structural signatures of residual force enhancement in myofibers.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Dynamic control of contractile resistance to iPSC-derived micro-heart muscle arrays.Journal of biomedical materials research. Part A · 2024
    Article
  18. Article
  19. Structure of mavacamten-free human cardiac thick filaments within the sarcomere by cryoelectron tomography.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  20. CaScientific reports · 2024
    Article

29 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

L FusiRandall Division of Cell and Molecular Biophysics and BHF Centre of Research Excellence, King's College London, London SE1 1UL UK.ORCID 0000-0003-3992-0114
E BrunelloRandall Division of Cell and Molecular Biophysics and BHF Centre of Research Excellence, King's College London, London SE1 1UL UK.ORCID 0000-0003-3167-4828
Z YanRandall Division of Cell and Molecular Biophysics and BHF Centre of Research Excellence, King's College London, London SE1 1UL UK.
M IrvingRandall Division of Cell and Molecular Biophysics and BHF Centre of Research Excellence, King's College London, London SE1 1UL UK.
King's College London · GB

Funding

British Heart FoundationMedical Research Council MR/M026655/1
6 · The paper itself

Abstract

Recent X-ray diffraction studies on actively contracting fibres from skeletal muscle showed that the number of myosin motors available to interact with actin-containing thin filaments is controlled by the stress in the myosin-containing thick filaments. Those results suggested that thick filament mechano-sensing might constitute a novel regulatory mechanism in striated muscles that acts independently of the well-known thin filament-mediated calcium signalling pathway. Here we test that hypothesis using probes attached to the myosin regulatory light chain in demembranated muscle fibres. We show that both the extent and kinetics of thick filament activation depend on thick filament stress but are independent of intracellular calcium concentration in the physiological range. These results establish direct control of myosin motors by thick filament mechano-sensing as a general regulatory mechanism in skeletal muscle that is independent of the canonical calcium signalling pathway.

Indexed as

Calcium SignalingAnimalsCalciumKineticsMaleMuscle, SkeletalMyosinsPhosphorylationPressurePsoas MusclesRabbitsSarcomeresSignal TransductionTime FactorsX-Ray DiffractionCalciumMyosins

Identifiers

PMID27796302
PMCPMC5095582
OpenAlexW2545141121

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.