Evidence map›Paper›PMID 24275437›Full record

ArticleJournal of biomechanics2014

The mechanical microenvironment of high concentration agarose for applying deformation to primary chondrocytes.

Donald L Zignego, Aaron A Jutila, Martin K Gelbke, Daniel M Gannon, Ronald K June

Abstract read
In one paragraph

Article in Journal of biomechanics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

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  7. A 3-D constitutive model for finite element analyses of agarose with a range of gel concentrations.Journal of the mechanical behavior of biomedical materials · 2021
    Article
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  11. [Study on the effect of artificial cartilage with different elastic modulus on the mechanical environment of the chondrocyte in defect cartilage repaired area].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2017
    Article
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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

5 authors at 2 institutions in 1 country.

Donald L ZignegoDepartment of Mechanical and Industrial Engineering, Montana State University, Bozeman, MT 59718-3800, USA.
Aaron A JutilaDepartment of Mechanical and Industrial Engineering, Montana State University, Bozeman, MT 59718-3800, USA.
Martin K GelbkeBridger Orthopedic and Sports Medicine, Bozeman, MT 59715, USA.
Daniel M GannonBridger Orthopedic and Sports Medicine, Bozeman, MT 59715, USA.
Ronald K JuneDepartment of Mechanical and Industrial Engineering, Montana State University, Bozeman, MT 59718-3800, USA; Department of Cell Biology and Neuroscience, Montana State University, Bozeman, MT 59718-3800, USA. Electronic address: rjune@me.montana.edu.
Montana State University · USBridger Photonics (United States) · US

Funding

Center for the Analysis of Cellular Mechanisms and Systems BiologyP20GM103394 · NIGMS · MONTANA STATE UNIVERSITY - BOZEMAN · PI DRATZ, EDWARD A · 2012 to 2013
$3.2M
NIGMS NIH HHS P20 GM103394NIGMS NIH HHS P20GM103394
6 · The paper itself

Abstract

Cartilage and chondrocytes experience loading that causes alterations in chondrocyte biological activity. In vivo chondrocytes are surrounded by a pericellular matrix with a stiffness of ~25-200kPa. Understanding the mechanical loading environment of the chondrocyte is of substantial interest for understanding chondrocyte mechanotransduction. The first objective of this study was to analyze the spatial variability of applied mechanical deformations in physiologically stiff agarose on cellular and sub-cellular length scales. Fluorescent microspheres were embedded in physiologically stiff agarose hydrogels. Microsphere positions were measured via confocal microscopy and used to calculate displacement and strain fields as a function of spatial position. The second objective was to assess the feasibility of encapsulating primary human chondrocytes in physiologically stiff agarose. The third objective was to determine if primary human chondrocytes could deform in high-stiffness agarose gels. Primary human chondrocyte viability was assessed using live-dead imaging following 24 and 72h in tissue culture. Chondrocyte shape was measured before and after application of 10% compression. These data indicate that (1) displacement and strain precision are ~1% and 6.5% respectively, (2) high-stiffness agarose gels can maintain primary human chondrocyte viability of >95%, and (3) compression of chondrocytes in 4.5% agarose can induce shape changes indicative of cellular compression. Overall, these results demonstrate the feasibility of using high-concentration agarose for applying in vitro compression to chondrocytes as a model for understanding how chondrocytes respond to in vivo loading.

Indexed as

SepharoseCells, CulturedCell SurvivalChondrocytesHumansMechanotransduction, CellularMicroscopy, ConfocalStress, MechanicalSepharoseChondrocyteConfocal microscopyFinite deformationMechanotransductionOsteoarthritis

Identifiers

PMID24275437
PMCPMC4014520
OpenAlexW2032713074

What OpenQuestion holds

Textmetadata
LicenceTDM
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.