Evidence map›Paper›PMID 25900674›Full record

ArticleJournal of dermatological science2015

Connexin 43 deficiency accelerates skin wound healing and extracellular matrix remodeling in mice.

Bruno Cogliati, Mathieu Vinken, Tereza C Silva, Cintia M M Araújo, Thiago P A Aloia, Lucas M Chaible, Cláudia M C Mori, Maria L Z Dagli

Open access · greenAbstract read
In one paragraph

Article in Journal of dermatological science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. The connexin 43 carboxyl terminal mimetic peptide αCT1 prompts differentiation of a collagen scar matrix in humans resembling unwounded skin.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Trial
  3. Trial
  4. Macrophage-Fibroblast Crosstalk Shapes Wound Repair Signaling In Vitro.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  5. Macrophages sense and follow physiologically relevant KCell communication and signaling : CCS · 2026
    Article
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  9. Review
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  15. Review
  16. Article
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  18. Article
  19. Connexin 43-Based Therapeutics for Dermal Wound Healing.International journal of molecular sciences · 2018
    Review
  20. 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

8 authors at 2 institutions in 2 countries.

Bruno Cogliati *Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo (USP), Brazil.
Mathieu Vinken *Department of In Vitro Toxicology and Dermato-Cosmetology, Vrije Universiteit Brussel (VUB), Brussels, Belgium.
Tereza C SilvaDepartment of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo (USP), Brazil.
Cintia M M AraújoDepartment of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo (USP), Brazil.
Thiago P A AloiaDepartment of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo (USP), Brazil.
Lucas M ChaibleDepartment of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo (USP), Brazil.
Cláudia M C MoriDepartment of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo (USP), Brazil.
Maria L Z DagliDepartment of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo (USP), Brazil.
Universidade de São Paulo · BRVrije Universiteit Brussel · BE

Funding

European Research Council 335476
6 · The paper itself

Abstract

backgroundCellular channels composed of connexin 43 are known to act as key players in the life cycle of the skin and consequently to underlie skin repair.

objectiveThis study was specifically set up to investigate the suite of molecular mechanisms driven by connexin 43-based channels on wound healing.

methodsTo this end, a battery of parameters, including re-epithelialization, neovascularization, collagen deposition and extracellular matrix remodeling, was monitored over time during experimentally induced skin repair in heterozygous connexin 43 knockout mice.

resultsIt was found that connexin 43 deficiency accelerates re-epithelialization and wound closure, increases proliferation and activation of dermal fibroblasts, and enhances the expression of extracellular matrix remodeling mediators.

conclusionThese data substantiate the notion that connexin 43 may represent an interesting therapeutic target in dermal wound healing.

Indexed as

AnimalsCell ProliferationCollagenConnexin 43Extracellular MatrixFibroblastsHeterozygoteMaleMiceMice, KnockoutNeovascularization, PhysiologicRe-EpithelializationCollagenConnexin 43Connexin 43Gap junctionSkin repairWound healing

Identifiers

PMID25900674
PMCPMC4450104
OpenAlexW1977897374

What OpenQuestion holds

Textmetadata
LicenceTDM
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.