Evidence map›Paper›PMID 27378743›Full record

ArticleGene2016

The synovial microenvironment of osteoarthritic joints alters RNA-seq expression profiles of human primary articular chondrocytes.

Eric A Lewallen, Carolina A Bonin, Xin Li, Jay Smith, Marcel Karperien, A Noelle Larson, David G Lewallen, Simon M Cool, Jennifer J Westendorf, Aaron J Krych and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Gene, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 21 citations in OpenAlex.

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  17. Transcriptional profiling of articular cartilage in a porcine model of early post-traumatic osteoarthritis.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2018
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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

13 authors at 5 institutions in 3 countries.

Eric A LewallenDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN, United States. Electronic address: lewallen.eric@mayo.edu.
Carolina A BoninDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN, United States. Electronic address: bonin.carolina@mayo.edu.
Xin LiJesse Brown VA Medical Center, Chicago, IL, United States. Electronic address: xin_li@rush.edu.
Jay SmithDepartment of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, MN, United States. Electronic address: smith.jay@mayo.edu.
Marcel KarperienDepartment of Developmental Bioengineering, University of Twente, Enschede, The Netherlands. Electronic address: h.b.j.karperien@utwente.nl.
A Noelle LarsonDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN, United States. Electronic address: larson.noelle@mayo.edu.
David G LewallenDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN, United States. Electronic address: lewallen.david@mayo.edu.
Simon M CoolDepartment of Orthopedic Surgery, National University of Singapore, Singapore. Electronic address: simon.cool@imb.a-star.edu.sg.
Jennifer J WestendorfDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN, United States; Department of Biochemistry & Molecular Biology, Mayo Clinic, Rochester, MN, United States. Electronic address: westendorf.jennifer@mayo.edu.
Aaron J KrychDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN, United States. Electronic address: krych.aaron@mayo.edu.
Alexey A LeontovichDepartment of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, United States. Electronic address: leontovich.alexey@mayo.edu.
Hee-Jeong ImJesse Brown VA Medical Center, Chicago, IL, United States; Department of Biochemistry, Rush University, Chicago, IL, United States; Department of Orthopedic Surgery, Rush University, Chicago, IL, United States; Department of Internal Medicine, Rush University, Chicago, IL, United States. Electronic address: Hee-Jeong_Sampen@rush.edu.
Andre J van WijnenDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, MN, United States; Department of Biochemistry & Molecular Biology, Mayo Clinic, Rochester, MN, United States; Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, United States. Electronic address: vanwijnen.andre@mayo.edu.
Mayo Clinic · USJesse Brown VA Medical Center · USNational University of Singapore · SGRush University Medical Center · USUniversity of Twente · NL

Funding

Musculoskeletal Research Training ProgramT32AR056950 · NIAMS · MAYO CLINIC ROCHESTER · PI Jennifer J Westendorf · 2009 to 2026
$7.0M
Molecular Control of Bone FormationR01AR049069 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WESTENDORF, JENNIFER J · 2003 to 2021
$5.8M
Runx2 and Axin2 Interactions During Bone FormationR01DE020194 · NIDCR · MAYO CLINIC ROCHESTER · PI WESTENDORF, JENNIFER J · 2010 to 2014
$2.1M
Protein Phosphatase Phlpp1 in Cartilage Development & Osteoarthritis ProgressionR01AR068103 · NIAMS · MAYO CLINIC ROCHESTER · PI WESTENDORF, JENNIFER J · 2014 to 2018
$1.9M
Pain Mechanisms of Knee Joint OsteoarthritisR01AR062136 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI CHEN, DI · 2012 to 2016
$1.7M
Epigenetic Modulation of the Epiphyseal Growth Plate to Treat Pediatric Limb DeformitiesR03AR066342 · NIAMS · MAYO CLINIC ROCHESTER · PI LARSON, ANNALISE NOELLE · 2014 to 2016
$239k
OSTEOARTHRITIS AND KNEE JOINT PAINI01BX002647 · VA · JESSE BROWN VA MEDICAL CENTER · PI SAMPEN, HEE-JEONG IM · 2015 to 2023
–
BLRD VA I01 BX002647NIAMS NIH HHS R01 AR049069NIAMS NIH HHS R01 AR062136NIAMS NIH HHS R01 AR068103NIAMS NIH HHS R03 AR066342NIAMS NIH HHS T32 AR056950NIDCR NIH HHS R01 DE020194
6 · The paper itself

Abstract

Osteoarthritis (OA) is a disabling degenerative joint disease that prompts pain and has limited treatment options. To permit early diagnosis and treatment of OA, a high resolution mechanistic understanding of human chondrocytes in normal and diseased states is necessary. In this study, we assessed the biological effects of OA-related changes in the synovial microenvironment on chondrocytes embedded within anatomically intact cartilage from joints with different pathological grades by next generation RNA-sequencing (RNA-seq). We determined the transcriptome of primary articular chondrocytes derived from anatomically unaffected knees and ankles, as well as from joints affected by OA. The GALAXY bioinformatics platform was used to facilitate biological interpretations. Comparisons of patient samples by k-means, hierarchical clustering and principal component analyses together reveal that primary chondrocytes exhibit OA grade-related differences in gene expression, including genes involved in cell-adhesion, ECM production and immune response. We conclude that diseased synovial microenvironments in joints with different histopathological OA grades directly alter gene expression in chondrocytes. One ramification of this finding is that anatomically intact cartilage from OA joints is not an ideal source of healthy chondrocytes, nor should these specimens be used to generate a normal baseline for the molecular characterization of diseased joints.

Indexed as

AgedCartilage, ArticularChondrocytesCohort StudiesFemaleGene Expression ProfilingHumansJointsMaleMiddle AgedOsteoarthritisSequence Analysis, RNACartilageCell adhesionCollins gradeECMGalaxy

Identifiers

PMID27378743
PMCPMC5989726
OpenAlexW2469765656

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.