Evidence map›Paper›PMID 18759278›Full record

ArticleArthritis and rheumatism2008

Rho kinase-dependent CCL20 induced by dynamic compression of human chondrocytes.

Dominik R Haudenschild, Bao Nguyen, Jianfen Chen, Darryl D D'Lima, Martin K Lotz

Open access · greenAbstract read
In one paragraph

Article in Arthritis and rheumatism, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 47 citations in OpenAlex.

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  12. RhoA/ROCK pathway: implication in osteoarthritis and therapeutic targets.American journal of translational research · 2019
    Review
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  17. Cyclic compression-induced p38 activation and subsequent MMP13 expression requires Rho/ROCK activity in bovine cartilage explants.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2012
    Article
  18. Article
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  20. Vimentin contributes to changes in chondrocyte stiffness in osteoarthritis.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2011
    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 at 2 institutions in 1 country.

Dominik R HaudenschildScripps Research Institute, and Scripps Clinic, La Jolla, California 92037, USA.
Bao Nguyen
Jianfen Chen
Darryl D D'Lima
Martin K Lotz
Scripps Health · USScripps Research Institute · US

Funding

TISSUE ACQUISITION, MORPHOLOGY, AND CELL CULTUREP01AG007996 · NIA · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI SAH, ROBERT L · 1989 to 2016
$26.0M
NIA NIH HHS AG-07996NIA NIH HHS P01 AG007996
6 · The paper itself

Abstract

objectiveMechanical stimulation of cartilage affects tissue homeostasis and chondrocyte function. The chondrocyte phenotype is dependent on cell shape, which is largely determined by the actin cytoskeleton. Reorganization of the actin cytoskeleton results from Rho GTPase activation. The purpose of this study was to examine the roles of both actin and Rho in mechanotransduction in chondrocytes.

methodsWe embedded human articular chondrocytes in 2 x 6-mm agarose discs at 5 x 10(6) cells/ml and subjected the discs to unconfined dynamic compression at 0.5 Hz. By comparing samples with and without dynamic compression, we identified Rho activation according to the GTP-bound active RhoA measured in cell lysates. We identified rearrangements in filamentous actin structures using fluorescence-labeled phalloidin and confocal microscopy of fixed samples. We identified altered gene expression using TaqMan quantitative reverse transcription-polymerase chain reaction analysis. We tested for a requirement for Rho signaling by performing the dynamic compression in the presence of Rho kinase inhibitors.

resultsRhoA activation occurred within 5-10 minutes of dynamic compression. Rho kinase-dependent actin reorganization occurred within 20 minutes after application of dynamic compression and was apparent as "punctate" F-actin structures that were visible under confocal microscopy. We identified early-phase mechanoresponsive genes (CCL20 and inducible nitric oxide synthase) that were highly up-regulated within 1 hour of dynamic compression in a Rho kinase-dependent and actin-dependent manner.

conclusionTogether, these results are the first demonstration that the Rho-Rho kinase pathway and actin cytoskeletal reorganization are required for changes in the expression of genes involved in human chondrocyte mechanotransduction.

Indexed as

1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineActinsAdolescentAdultCell Culture TechniquesCells, CulturedCell ShapeChemokine CCL20ChondrocytesCytoskeletonFemaleGene ExpressionHumansInterleukin-1betaMaleMechanotransduction, Cellular1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineActinsCCL20 protein, humanChemokine CCL20hydroxyfasudilInterleukin-1betaNitric Oxide Synthase Type IIrho-Associated KinasesRNA, Messenger

Identifiers

PMID18759278
PMCPMC2562294
OpenAlexW2088124208

What OpenQuestion holds

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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.