Evidence map›Paper›PMID 34214097›Full record

ArticlePloS one2021

Alpha and beta adrenergic receptors modulate keratinocyte migration.

Hsin-Ya Yang, Pieter Steenhuis, Aaron M Glucksman, Zhanna Gurenko, Thi Dinh La, R Rivkah Isseroff

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Immunomodulatory Tissue-Engineering Strategies for Diabetic Foot Ulcer Management: A Systematic Review.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Synthesis,Journal of enzyme inhibition and medicinal chemistry · 2023
    Article
  8. Review
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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

6 authors at 2 institutions in 1 country.

Hsin-Ya YangDepartment of Dermatology, University of California, Davis, Davis, California, United States of America.ORCID 0000-0002-5325-494X
Pieter SteenhuisDepartment of Dermatology, University of California, Davis, Davis, California, United States of America.
Aaron M GlucksmanDepartment of Dermatology, University of California, Davis, Davis, California, United States of America.
Zhanna GurenkoDepartment of Dermatology, University of California, Davis, Davis, California, United States of America.
Thi Dinh LaDepartment of Dermatology, University of California, Davis, Davis, California, United States of America.
R Rivkah IsseroffDepartment of Dermatology, University of California, Davis, Davis, California, United States of America.ORCID 0000-0001-7813-0858
University of California, Davis · USVA Northern California Health Care System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Keratinocyte migration into skin wounds is the step of the healing process that correlates with the wound closure rate. Keratinocyte migration, and wound epithelialization are decreased when beta 2-adrenergic receptors (B2AR) are activated by 1 μM epinephrine/adrenaline, resulting in delayed wound healing in human and mouse skin. In the present study, we found paradoxically, that in a subset of keratinocyte strains exposure to low concentrations of epinephrine (0.1 nM) increased, rather than decreased, their migratory rate. We find that both the alpha- and the beta-adrenergic receptors are expressed in human keratinocytes, and expression of alpha-2 AR subtypes demonstrated for the first time. Therefore, we tested if the alpha-AR could be modulating the increased migratory response observed in these cell strains. By using specific inhibitors to alpha-AR, we demonstrated that blocking A2B-AR could reverse the rapid cell migration induced by the 0.1 nM epinephrine. Phosphorylation of ERK was elevated after 1-10 minutes of the low epinephrine treatment and the A2B-AR inhibitor blocked the ERK phosphorylation. The results suggest that both the A2B-AR and B2AR mediate keratinocyte migration, in which with a low level of epinephrine treatment, A2B-AR could alter the B2AR signals and regulate the migration rate.

Indexed as

Cell MovementHumansInfant, NewbornKeratinocytesMaleReceptors, Adrenergic, alphaReceptors, Adrenergic, betaWound HealingReceptors, Adrenergic, alphaReceptors, Adrenergic, beta

Identifiers

PMID34214097
PMCPMC8253387
OpenAlexW3174266874

What Socratic holds

Textmetadata
LicenceCC0
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 Socratic graph.