Evidence map›Paper›PMID 29472541›Full record

ArticleNature communications2018

Periosteum contains skeletal stem cells with high bone regenerative potential controlled by Periostin.

Oriane Duchamp de Lageneste, Anaïs Julien, Rana Abou-Khalil, Giulia Frangi, Caroline Carvalho, Nicolas Cagnard, Corinne Cordier, Simon J Conway, Céline Colnot

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 328 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
328citing papers in PubMed, 1 pooled it
48.5field-weighted citation impact, top 1% 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

328 citing papers in PubMed, 1 synthesis or guideline pooled it, 541 citations in OpenAlex.

  1. Pooled it
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  7. Identification and characterization of POSTNJournal of orthopaedic translation · 2026
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  12. Clec3bBone research · 2026
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268 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 2 countries.

Oriane Duchamp de LagenesteINSERM UMR1163, Imagine Institute, Paris Descartes University, 75015, Paris, France.
Anaïs JulienINSERM UMR1163, Imagine Institute, Paris Descartes University, 75015, Paris, France.
Rana Abou-KhalilINSERM UMR1163, Imagine Institute, Paris Descartes University, 75015, Paris, France.
Giulia FrangiINSERM UMR1163, Imagine Institute, Paris Descartes University, 75015, Paris, France.
Caroline CarvalhoINSERM UMR1163, Imagine Institute, Paris Descartes University, 75015, Paris, France.
Nicolas CagnardParis-Descartes Bioinformatics Platform, 75015, Paris, France.
Corinne CordierINSERM US24 - CNRS UMS3633 Cytometry Platform, Paris Descartes University, 75015, Paris, France.
Simon J ConwayHerman B. Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Céline ColnotINSERM UMR1163, Imagine Institute, Paris Descartes University, 75015, Paris, France. celine.colnot@inserm.fr.ORCID http://orcid.org/0000-0001-8423-8718
Inserm · FRDélégation Paris 5 · FRIndiana University School of Medicine

Funding

Functional roles of muscle in bone repairR01AR057344 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MICLAU, THEODORE · 2010 to 2014
$1.7M
NIAMS NIH HHS R01 AR057344
6 · The paper itself

Abstract

Bone regeneration relies on the activation of skeletal stem cells (SSCs) that still remain poorly characterized. Here, we show that periosteum contains SSCs with high bone regenerative potential compared to bone marrow stromal cells/skeletal stem cells (BMSCs) in mice. Although periosteal cells (PCs) and BMSCs are derived from a common embryonic mesenchymal lineage, postnatally PCs exhibit greater clonogenicity, growth and differentiation capacity than BMSCs. During bone repair, PCs can efficiently contribute to cartilage and bone, and integrate long-term after transplantation. Molecular profiling uncovers genes encoding Periostin and other extracellular matrix molecules associated with the enhanced response to injury of PCs. Periostin gene deletion impairs PC functions and fracture consolidation. Periostin-deficient periosteum cannot reconstitute a pool of PCs after injury demonstrating the presence of SSCs within periosteum and the requirement of Periostin in maintaining this pool. Overall our results highlight the importance of analyzing periosteum and PCs to understand bone phenotypes.

Indexed as

Bone RegenerationAnimalsCell Adhesion MoleculesFemaleMaleMiceMice, Inbred C57BLMice, KnockoutOsteogenesisPeriosteumStem CellsStromal CellsCell Adhesion MoleculesPostn protein, mouse

Identifiers

PMID29472541
PMCPMC5823889
OpenAlexW2790664419

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.