Evidence map›Paper›PMID 20398806›Full record

ArticleActa biomaterialia2010

Regulation of keratinocyte signaling and function via changes in epidermal growth factor presentation.

Tracy J Puccinelli, Paul J Bertics, Kristyn S Masters

Abstract read
In one paragraph

Article in Acta biomaterialia, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.2field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Statistic Copolymers Working as Growth Factor-Binding Mimics of Fibronectin.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Article
  6. Chemical Composition ofPlants (Basel, Switzerland) · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Engineering Approaches to Study Cellular Decision Making.Annual review of biomedical engineering · 2018
    Review
  12. Article
  13. Immobilized epidermal growth factor stimulates persistent, directed keratinocyte migration via activation of PLCγ1.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. 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

3 authors at 1 institution in 1 country.

Tracy J PuccinelliMaterials Science Program, University of Wisconsin, Madison, WI 53706, USA.
Paul J Bertics
Kristyn S Masters
University of Wisconsin–Madison · US

Funding

Micropatterned EGF of Accelerated Wound HealingR21EB005440 · NIBIB · UNIVERSITY OF WISCONSIN-MADISON · PI MASTERS, KRISTYN S · 2006 to 2007
$379k
NIBIB NIH HHS 1R21-EB005440NIBIB NIH HHS R21 EB005440
6 · The paper itself

Abstract

Motivated by the need for bioactive materials that can accelerate dermal wound healing, this work describes the responses of keratinocytes to covalently immobilized epidermal growth factor (EGF) and how differences in the physical presentation of this growth factor affect cell function. Specifically, human keratinocytes were cultured with EGF delivered in soluble form, immobilized in a homogeneous pattern or immobilized in a gradient pattern, followed by analysis of cellular signaling, proliferation and migration. By changing the manner in which EGF was presented, keratinocyte behavior was dramatically altered. Keratinocytes responded to immobilized EGF patterns with high EGF receptor (EGFR) but low ERK1/2 and Akt phosphorylation, accompanied by low proliferation, high migratory activity and coordinated cell alignment. In contrast, keratinocytes treated with soluble EGF experienced lower EGFR but higher ERK1/2 and Akt phosphorylation and displayed a highly proliferative, rather than migratory, phenotype. Keratinocytes also responded to differences in immobilized EGF patterns, as migration was fastest upon immobilized gradients of EGF. A better understanding the interaction of cells with soluble vs. immobilized growth factors can help elucidate native healing events and achieve greater control over cell function, which may be useful in the development of wound repair treatments for many types of tissues.

Indexed as

Cell MovementCell ProliferationCells, CulturedEpidermal Growth FactorErbB ReceptorsExtracellular Signal-Regulated MAP KinasesHumansImmobilized ProteinsKeratinocytesLightPhosphorylationProto-Oncogene Proteins c-aktSignal TransductionSolubilityEpidermal Growth FactorErbB ReceptorsExtracellular Signal-Regulated MAP KinasesImmobilized ProteinsProto-Oncogene Proteins c-akt

Identifiers

PMID20398806
PMCPMC2910130
OpenAlexW2018609083

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.