Evidence map›Paper›PMID 34581667›Full record

ArticleeLife2021

Age-dependent changes in protein incorporation into collagen-rich tissues of mice by in vivo pulsed SILAC labelling.

Yoanna Ariosa-Morejon, Alberto Santos, Roman Fischer, Simon Davis, Philip Charles, Rajesh Thakker, Angus Kt Wann, Tonia L Vincent

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

  1. Mass spectrometry proteomics for studying mitostasis.Protein science : a publication of the Protein Society · 2026
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  9. Mechanisms of assembly and remodelling of the extracellular matrix.Nature reviews. Molecular cell biology · 2024
    Review
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  11. A quantitativeMethodsX · 2023
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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

8 authors at 4 institutions in 3 countries.

Yoanna Ariosa-MorejonKennedy Institute of Rheumatology, Arthritis Research UK Centre for OA Pathogenesis, University of Oxford, Oxford, United Kingdom.
Alberto SantosBig Data Institute, Li-Ka Shing Centre for Health Information and Discovery, University of Oxford, Oxford, United Kingdom.
Roman FischerNuffield Department of Medicine, Target Discovery Institute, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-9715-5951
Simon DavisNuffield Department of Medicine, Target Discovery Institute, University of Oxford, Oxford, United Kingdom.
Philip CharlesNuffield Department of Medicine, Target Discovery Institute, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-5278-5354
Rajesh ThakkerAcademic Endocrine Unit, OCDEM, Churchill Hospital, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-1438-3220
Angus Kt WannKennedy Institute of Rheumatology, Arthritis Research UK Centre for OA Pathogenesis, University of Oxford, Oxford, United Kingdom.
Tonia L VincentKennedy Institute of Rheumatology, Arthritis Research UK Centre for OA Pathogenesis, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-3412-5712
Target (United States) · USUniversity of Oxford · GBChurchill Hospital · GBUniversity of Copenhagen · DK

Funding

Versus Arthritis 20205Versus Arthritis 21621
6 · The paper itself

Abstract

Collagen-rich tissues have poor reparative capacity that predisposes to common age-related disorders such as osteoporosis and osteoarthritis. We used in vivo pulsed SILAC labelling to quantify new protein incorporation into cartilage, bone, and skin of mice across the healthy life course. We report dynamic turnover of the matrisome, the proteins of the extracellular matrix, in bone and cartilage during skeletal maturation, which was markedly reduced after skeletal maturity. Comparing young adult with older adult mice, new protein incorporation was reduced in all tissues. STRING clustering revealed changes in epigenetic modulators across all tissues, a decline in chondroprotective growth factors such as FGF2 and TGFβ in cartilage, and clusters indicating mitochondrial dysregulation and reduced collagen synthesis in bone. Several pathways were implicated in age-related disease. Fewer changes were observed for skin. This methodology provides dynamic protein data at a tissue level, uncovering age-related molecular changes that may predispose to disease.

Indexed as

Age FactorsAnimalsBone and BonesBone DevelopmentCartilage, ArticularCollagenEpigenesis, GeneticFibroblast Growth Factor 2MaleMass SpectrometryMiceMice, Inbred C57BLProteinsProteomeSkinTransforming Growth Factor betaCollagenFibroblast Growth Factor 2ProteinsProteomeTransforming Growth Factor betaAgecell biologycollagen-rich tissuesmatrisomemouseprotein dynamicsproteomicsSILAC

Identifiers

PMID34581667
PMCPMC8478409
OpenAlexW3204621535

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.