Evidence map›Paper›PMID 31654035›Full record

ArticleCell death and differentiation2020

Autologous micrograft accelerates endogenous wound healing response through ERK-induced cell migration.

Martina Balli, Francesca Vitali, Adrian Janiszewski, Ellen Caluwé, Alvaro Cortés-Calabuig, Sebastien Carpentier, Robin Duelen, Flavio Ronzoni, Lukas Marcelis, Francesca Maria Bosisio and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.3field-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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. From Time to Timer in Wound Healing Through the Regeneration.Advances in experimental medicine and biology · 2024
    Review
  8. Article
  9. FastSkinJournal of clinical medicine · 2023
    Article
  10. Review
  11. Article
  12. Analytical cellular pathology (Amsterdam) · 2023
    Article
  13. Sprayed PAA-CaORegenerative biomaterials · 2023
    Article
  14. Article
  15. Mechanistic Wound Healing and Antioxidant Potential ofAntioxidants (Basel, Switzerland) · 2022
    Article
  16. Article
  17. Article
  18. 3D bioprinting and RigeneraFrontiers in bioengineering and biotechnology · 2022
    Article
  19. Article
  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

16 authors at 4 institutions in 3 countries.

Martina BalliDepartment of Development and Regeneration, Stem Cell Institute, KU Leuven, B-3000, Leuven, Belgium.
Francesca VitaliCenter for Biomedical Informatics and Biostatistics, The University of Arizona Health Sciences, Tucson, AZ, USA.
Adrian JaniszewskiDepartment of Development and Regeneration, Stem Cell Institute, KU Leuven, B-3000, Leuven, Belgium.
Ellen CaluwéDepartment of Cardiovascular Sciences, Centre for Molecular and Vascular Biology, KU Leuven, B-3000, Leuven, Belgium.
Alvaro Cortés-CalabuigGenomics Core Leuven, Centre for Human Genetics KU Leuven, 3000, Leuven, Belgium.
Sebastien CarpentierFacility for SYstems BIOlogy based MAss sepctrometry, KU Leuven, 3000, Leuven, Belgium.
Robin DuelenDepartment of Development and Regeneration, Stem Cell Institute, KU Leuven, B-3000, Leuven, Belgium.ORCID http://orcid.org/0000-0003-0904-1215
Flavio RonzoniHuman Anatomy Unit, Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.
Lukas MarcelisTranslational Cell and Tissue Research Lab, Department of Imaging and Pathology, KU Leuven, Leuven, Belgium.
Francesca Maria BosisioTranslational Cell and Tissue Research Lab, Department of Imaging and Pathology, KU Leuven, Leuven, Belgium.
Riccardo BellazziCenter for Health Technologies (CHT), University of Pavia, Pavia, Italy.
Aernout LuttunDepartment of Cardiovascular Sciences, Centre for Molecular and Vascular Biology, KU Leuven, B-3000, Leuven, Belgium.
Maria G Cusella De AngelisHuman Anatomy Unit, Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.
Gabriele CeccarelliHuman Anatomy Unit, Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.
Frederic Lluis *Department of Development and Regeneration, Stem Cell Institute, KU Leuven, B-3000, Leuven, Belgium. frederic.lluisvinas@kuleuven.be.
Maurilio Sampaolesi *Department of Development and Regeneration, Stem Cell Institute, KU Leuven, B-3000, Leuven, Belgium. maurilio.sampaolesi@kuleuven.be.ORCID http://orcid.org/0000-0002-2422-3757
KU Leuven · BEUniversity of Pavia · ITRega Institute for Medical Research · BEUniversity of Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defective cell migration causes delayed wound healing (WH) and chronic skin lesions. Autologous micrograft (AMG) therapies have recently emerged as a new effective and affordable treatment able to improve wound healing capacity. However, the precise molecular mechanism through which AMG exhibits its beneficial effects remains unrevealed. Herein we show that AMG improves skin re-epithelialization by accelerating the migration of fibroblasts and keratinocytes. More specifically, AMG-treated wounds showed improvement of indispensable events associated with successful wound healing such as granulation tissue formation, organized collagen content, and newly formed blood vessels. We demonstrate that AMG is enriched with a pool of WH-associated growth factors that may provide the starting signal for a faster endogenous wound healing response. This work links the increased cell migration rate to the activation of the extracellular signal-regulated kinase (ERK) signaling pathway, which is followed by an increase in matrix metalloproteinase expression and their extracellular enzymatic activity. Overall we reveal the AMG-mediated wound healing transcriptional signature and shed light on the AMG molecular mechanism supporting its potential to trigger a highly improved wound healing process. In this way, we present a framework for future improvements in AMG therapy for skin tissue regeneration applications.

Indexed as

Cell MovementSkin TransplantationWound HealingAnimalsCells, CulturedExtracellular Signal-Regulated MAP KinasesFemaleFibroblastsGene Expression ProfilingGene Regulatory NetworksKeratinocytesMAP Kinase Signaling SystemMatrix MetalloproteinasesMice, Inbred C57BLSolubilityTranscription, GeneticExtracellular Signal-Regulated MAP KinasesMatrix Metalloproteinases

Identifiers

PMID31654035
PMCPMC7206041
OpenAlexW2981555932

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.