Evidence map›Paper›PMID 31511609›Full record

ArticleScientific reports2019

Heterogeneity in The Mechanical Properties of Integrins Determines Mechanotransduction Dynamics in Bone Osteoblasts.

Aban Shuaib, Daniyal Motan, Pinaki Bhattacharya, Alex McNabb, Timothy M Skerry, Damien Lacroix

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

28 citing papers in PubMed, 33 citations in OpenAlex.

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  19. Treatment of ischemic stroke with modified mesenchymal stem cells.International journal of medical sciences · 2022
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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

6 authors at 2 institutions in 1 country.

Aban ShuaibDepartment of Oncology and Metabolism, University of Sheffield, Sheffield, UK. aban.shuaib@sheffield.ac.uk.
Daniyal MotanDepartment of Mechanical Engineering, University of Sheffield, Sheffield, UK.
Pinaki BhattacharyaInsigneo Institute for in silico Medicine, University of Sheffield, Sheffield, UK.
Alex McNabbDepartment of Mechanical Engineering, University of Sheffield, Sheffield, UK.
Timothy M SkerryDepartment of Oncology and Metabolism, University of Sheffield, Sheffield, UK.
Damien LacroixInsigneo Institute for in silico Medicine, University of Sheffield, Sheffield, UK.
University of Sheffield · GBInsigneo · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone cells are exposed to dynamic mechanical stimulation that is transduced into cellular responses by mechanotransduction mechanisms. The extracellular matrix (ECM) provides a physical link between loading and bone cells, where mechanoreceptors, such as integrins, initiate mechanosensation. Though this relationship is well studied, the dynamic interplay between mechanosensation, mechanotransduction and cellular responses is unclear. A hybrid-multiscale model combining molecular, cellular and tissue interactions was developed to examine links between integrins' mechanosensation and effects on mechanotransduction, ECM modulation and cell-ECM interaction. The model shows that altering integrin mechanosensitivity threshold (MT) increases mechanotransduction durations from hours to beyond 4 days, where bone formation starts. This is relevant to bone, where it is known that a brief stimulating period provides persistent influences for over 24 hours. Furthermore, the model forecasts that integrin heterogeneity, with respect to MT, would be able to induce sustained increase in pERK baseline > 15% beyond 4 days. This is analogous to the emergence of molecular mechanical memory signalling dynamics. Therefore, the model can provide a greater understanding of mechanical adaptation to differential mechanical responses at different times. Given reduction of bone sensitivity to mechanical stimulation with age, these findings may lead towards useful therapeutic targets for upregulation of bone mass.

Indexed as

Mechanotransduction, CellularModels, TheoreticalStress, MechanicalAnimalsBone and BonesCells, CulturedExtracellular MatrixHumansIntegrinsMechanoreceptorsOsteoblastsSignal TransductionIntegrins

Identifiers

PMID31511609
PMCPMC6739315
OpenAlexW2973047143

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.