Evidence map›Paper›PMID 32658450›Full record

ArticleACS nano2020

Nanovibrational Stimulation of Mesenchymal Stem Cells Induces Therapeutic Reactive Oxygen Species and Inflammation for Three-Dimensional Bone Tissue Engineering.

Wich Orapiriyakul, Monica P Tsimbouri, Peter Childs, Paul Campsie, Julia Wells, Marc A Fernandez-Yague, Karl Burgess, K Elizabeth Tanner, Manlio Tassieri, Dominic Meek and 6 more

Abstract read
In one paragraph

Article in ACS nano, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

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  19. Static and Dynamic Biomaterial Engineering for Cell Modulation.Nanomaterials (Basel, Switzerland) · 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

16 authors.

Wich OrapiriyakulCentre for the Cellular Microenvironment, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary, and Life Sciences, University of Glasgow, Glasgow G12 8QQ, United Kingdom.
Monica P TsimbouriCentre for the Cellular Microenvironment, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary, and Life Sciences, University of Glasgow, Glasgow G12 8QQ, United Kingdom.
Peter ChildsCentre for the Cellular Microenvironment, Division of Biomedical Engineering, School of Engineering, University of Glasgow, Glasgow G12 8LT, United Kingdom.
Paul CampsieSUPA Department of Biomedical Engineering, University of Strathclyde, Glasgow G1 1QE, United Kingdom.
Julia WellsBone and Joint Research Group, Centre for Human Development, Stem Cells and Regeneration, Institute of Developmental Sciences, University of Southampton, Southampton SO16 6YD, United Kingdom.
Marc A Fernandez-YagueCentre for Research in Medical Devices (CÚRAM), National University of Ireland Galway, Galway, Ireland.
Karl BurgessGlasgow Polyomics, College of Medical, Veterinary, and Life Sciences, University of Glasgow, Switchback Rd, Bearsden, Glasgow G61 1BD, United Kingdom.
K Elizabeth TannerCentre for the Cellular Microenvironment, Division of Biomedical Engineering, School of Engineering, University of Glasgow, Glasgow G12 8LT, United Kingdom.ORCID 0000-0003-2257-0218
Manlio TassieriCentre for the Cellular Microenvironment, Division of Biomedical Engineering, School of Engineering, University of Glasgow, Glasgow G12 8LT, United Kingdom.ORCID 0000-0002-6807-0385
Dominic MeekDepartment of Orthopedics, Queen Elizabeth II University Hospital, Glasgow G51 4TF, United Kingdom.
Massimo VassalliCentre for the Cellular Microenvironment, Division of Biomedical Engineering, School of Engineering, University of Glasgow, Glasgow G12 8LT, United Kingdom.ORCID 0000-0002-3063-4376
Manus J P BiggsCentre for Research in Medical Devices (CÚRAM), National University of Ireland Galway, Galway, Ireland.
Manuel Salmeron-SanchezCentre for the Cellular Microenvironment, Division of Biomedical Engineering, School of Engineering, University of Glasgow, Glasgow G12 8LT, United Kingdom.ORCID 0000-0002-8112-2100
Richard O C OreffoBone and Joint Research Group, Centre for Human Development, Stem Cells and Regeneration, Institute of Developmental Sciences, University of Southampton, Southampton SO16 6YD, United Kingdom.
Stuart ReidSUPA Department of Biomedical Engineering, University of Strathclyde, Glasgow G1 1QE, United Kingdom.
Matthew J DalbyCentre for the Cellular Microenvironment, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary, and Life Sciences, University of Glasgow, Glasgow G12 8QQ, United Kingdom.ORCID 0000-0002-0528-3359

Funding

Biotechnology and Biological Sciences Research Council BB/P00220X/1Biotechnology and Biological Sciences Research Council BB/S018808/1
6 · The paper itself

Abstract

There is a pressing clinical need to develop cell-based bone therapies due to a lack of viable, autologous bone grafts and a growing demand for bone grafts in musculoskeletal surgery. Such therapies can be tissue engineered and cellular, such as osteoblasts, combined with a material scaffold. Because mesenchymal stem cells (MSCs) are both available and fast growing compared to mature osteoblasts, therapies that utilize these progenitor cells are particularly promising. We have developed a nanovibrational bioreactor that can convert MSCs into bone-forming osteoblasts in two- and three-dimensional, but the mechanisms involved in this osteoinduction process remain unclear. Here, to elucidate this mechanism, we use increasing vibrational amplitude, from 30 nm (N30) to 90 nm (N90) amplitudes at 1000 Hz and assess MSC metabolite, gene, and protein changes. These approaches reveal that dose-dependent changes occur in MSCs' responses to increased vibrational amplitude, particularly in adhesion and mechanosensitive ion channel expression and that energetic metabolic pathways are activated, leading to low-level reactive oxygen species (ROS) production and to low-level inflammation as well as to ROS- and inflammation-balancing pathways. These events are analogous to those that occur in the natural bone-healing processes. We have also developed a tissue engineered MSC-laden scaffold designed using cells' mechanical memory, driven by the stronger N90 stimulation. These mechanistic insights and cell-scaffold design are underpinned by a process that is free of inductive chemicals.

Indexed as

Mesenchymal Stem CellsCell DifferentiationHumansInflammationOsteogenesisReactive Oxygen SpeciesTissue EngineeringTissue ScaffoldsReactive Oxygen Speciesbioreactorbone tissue engineeringmechanotransductionmesenchymal stem cellsnanovibration

Identifiers

PMID32658450
PMCPMC7458485

What OpenQuestion holds

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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.