Evidence map›Paper›PMID 22266908›Full record

ArticleJournal of cell science2012

Periostin modulates myofibroblast differentiation during full-thickness cutaneous wound repair.

Christopher G Elliott, Jian Wang, Xiaolei Guo, Shi-wen Xu, Mark Eastwood, Jianjun Guan, Andrew Leask, Simon J Conway, Douglas W Hamilton

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
14.4field-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

80 citing papers in PubMed, 142 citations in OpenAlex.

  1. Article
  2. CRISPR-MediatedCells · 2026
    Article
  3. Article
  4. BMP2-induced Adam12International journal of biological sciences · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Clock gene Per2 modulates epidermal tissue repair in vivo.Journal of cellular biochemistry · 2024
    Article
  14. The role of periostin in cardiac fibrosis.Heart failure reviews · 2024
    Review
  15. Identification of Periostin as a critical niche for myofibroblast dynamics and fibrosis during tendon healing.Matrix biology : journal of the International Society for Matrix Biology · 2024
    Article
  16. Article
  17. Matricellular Proteins in the Homeostasis, Regeneration, and Aging of Skin.International journal of molecular sciences · 2023
    Review
  18. Article
  19. Matricellular proteins in cutaneous wound healing.Frontiers in cell and developmental biology · 2022
    Review
  20. Article

20 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 5 institutions in 3 countries.

Christopher G ElliottDepartment of Anatomy and Cell Biology, Schulich School of Medicine and Dentistry, The University of Western Ontario, London, Ontario, Canada.
Jian Wang
Xiaolei Guo
Shi-wen Xu
Mark Eastwood
Jianjun Guan
Andrew Leask
Simon J Conway
Douglas W Hamilton
Western University · CAIndiana University School of MedicineThe Ohio State University · USUniversity College London · GBUniversity of Westminster · GB

Funding

Regulation of Periostin by TGFbeta and BMP in Heart DevelopmentR01HL092508 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI CONWAY, SIMON JAMES, DOETSCHMAN, THOMAS · 2009 to 2010
$929k
Arthritis Research UKCIHR IMH-94010NHLBI NIH HHS HL092508NHLBI NIH HHS R01 HL092508
6 · The paper itself

Abstract

The matricellular protein periostin is expressed in the skin. Although periostin has been hypothesized to contribute to dermal homeostasis and repair, this has not been directly tested. To assess the contribution of periostin to dermal healing, 6 mm full-thickness excisional wounds were created in the skin of periostin-knockout and wild-type, sex-matched control mice. In wild-type mice, periostin was potently induced 5-7 days after wounding. In the absence of periostin, day 7 wounds showed a significant reduction in myofibroblasts, as visualized by expression of α-smooth muscle actin (α-SMA) within the granulation tissue. Delivery of recombinant human periostin by electrospun collagen scaffolds restored α-SMA expression. Isolated wild-type and knockout dermal fibroblasts did not differ in in vitro assays of adhesion or migration; however, in 3D culture, periostin-knockout fibroblasts showed a significantly reduced ability to contract a collagen matrix, and adopted a dendritic phenotype. Recombinant periostin restored the defects in cell morphology and matrix contraction displayed by periostin-deficient fibroblasts in a manner that was sensitive to a neutralizing anti-β1-integrin and to the FAK and Src inhibitor PP2. We propose that periostin promotes wound contraction by facilitating myofibroblast differentiation and contraction.

Indexed as

Cell DifferentiationWound HealingActinsAnimalsCell Adhesion MoleculesCell ShapeCollagenFocal Adhesion Kinase 1Granulation TissueIntegrin beta1KineticsMiceMice, KnockoutMuscle, SmoothMyofibroblastsSignal TransductionActinsCell Adhesion MoleculesCollagenFocal Adhesion Kinase 1Integrin beta1Postn protein, mousePtk2 protein, mousesrc-Family KinasesTransforming Growth Factor beta

Identifiers

PMID22266908
PMCPMC3269025
OpenAlexW2061627817

What OpenQuestion holds

Textmetadata
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.