Evidence map›Paper›PMID 27887728›Full record

ArticleJournal of biomechanics2016

Novel multi-functional fluid flow device for studying cellular mechanotransduction.

James S Lyons, Shama R Iyer, Richard M Lovering, Christopher W Ward, Joseph P Stains

Abstract read
In one paragraph

Article in Journal of biomechanics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Nitric oxide contributes to rapid sclerostin protein loss following mechanical load.Biochemical and biophysical research communications · 2024
    Article
  2. Article
  3. Bio-protocol · 2021
    Article
  4. Article
  5. Article
  6. Review
  7. The lymph node stromal laminin α5 shapes alloimmunity.The Journal of clinical investigation · 2020
    Article
  8. 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.

James S LyonsDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Shama R IyerDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Richard M LoveringDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Christopher W WardUniversity of Maryland School of Nursing, Baltimore, MD 21201, USA.
Joseph P StainsDepartment of Orthopaedics, University of Maryland School of Medicine, Baltimore, MD 21201, USA. Electronic address: jstains@som.umaryland.edu.

Funding

Interdisciplinary Training Program Muscle BiologyT32AR007592 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Aikaterini Kontrogianni-Konstantopoulos · 1996 to 2026
$11.7M
TRAINING PROGRAM IN INTEGRATIVE MEMBRANE BIOLOGYT32GM008181 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI RIZZO, MEGAN A, TRUDEAU, MATTHEW C · 1987 to 2022
$4.9M
Spatial Control of Bone Remodeling by Gap Junction-Communicated cAMPR01AR063631 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI STAINS, JOSEPH P. · 2013 to 2024
$3.3M
Mechanisms of Force Loss in Injured and Dystrophic Skeletal MuscleR01AR059179 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI LOVERING, RICHARD M · 2010 to 2014
$1.4M
Stretch Dependent Signaling in Dystrophic Skeletal MuscleR01AR062554 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI WARD, CHRISTOPHER WILLIAM · 2013 to 2014
$675k
NIAMS NIH HHS R01 AR059179NIAMS NIH HHS R01 AR062554NIAMS NIH HHS R01 AR063631NIAMS NIH HHS T32 AR007592NIGMS NIH HHS T32 GM008181
6 · The paper itself

Abstract

Cells respond to their mechanical environment by initiating multiple mechanotransduction signaling pathways. Defects in mechanotransduction have been implicated in a number of pathologies; thus, there is need for convenient and efficient methods for studying the mechanisms underlying these processes. A widely used and accepted technique for mechanically stimulating cells in culture is the introduction of fluid flow on cell monolayers. Here, we describe a novel, multifunctional fluid flow device for exposing cells to fluid flow in culture. This device integrates with common lab equipment including routine cell culture plates and peristaltic pumps. Further, it allows the fluid flow treated cells to be examined with outcomes at the cell and molecular level. We validated the device using the biologic response of cultured UMR-106 osteoblast-like cells in comparison to a commercially available system of laminar sheer stress to track live cell calcium influx in response to fluid flow. In addition, we demonstrate the fluid flow-dependent activation of phospho-ERK in these cells, consistent with the findings in other fluid flow devices. This device provides a low cost, multi-functional alternative to currently available systems, while still providing the ability to generate physiologically relevant conditions for studying processes involved in mechanotransduction in vitro.

Indexed as

Mechanotransduction, CellularAnimalsCalcium SignalingCell Culture TechniquesCells, CulturedCytophotometryHydrodynamicsOsteoblastsRatsSingle-Cell AnalysisBone cellsFluid shear stressIntracellular calciumMechanotransductionOsteoblastOsteocyteSignal transduction

Identifiers

PMID27887728
PMCPMC5164981

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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.