Evidence map›Paper›PMID 21811556›Full record

ArticlePloS one2011

Eosinophils increase neuron branching in human and murine skin and in vitro.

Erin L Foster, Eric L Simpson, Lorna J Fredrikson, James J Lee, Nancy A Lee, Allison D Fryer, David B Jacoby

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
6.1field-weighted citation impact, top 4% 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

51 citing papers in PubMed, 94 citations in OpenAlex.

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  16. Neurotrophins: Neuroimmune Interactions in Human Atopic Diseases.International journal of molecular sciences · 2023
    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

7 authors at 2 institutions in 1 country.

Erin L FosterDepartment of Molecular Microbiology and Immunology, Oregon Health & Science University, Portland, Oregon, United States of America.
Eric L Simpson
Lorna J Fredrikson
James J Lee
Nancy A Lee
Allison D Fryer
David B Jacoby
Oregon Health & Science University · USMayo Clinic in Arizona · US

Funding

EOSINOPHIL ACTIVITIES IN MURINE MODELS OF LUNG DISEASER01HL065228 · NHLBI · MAYO CLINIC COLL OF MED, MAYO CLINIC AZ · PI JACOBSEN, ELIZABETH A · 2000 to 2017
$6.7M
INTERACTIONS AT THE MICROBE/HOST INTERFACET32AI007472 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI LANDFEAR, SCOTT M · 1995 to 2019
$6.7M
MOUSE MODELS OF EOSINOPHIL ASSOCIATED LUNG DYSFUNCTIONR01HL058723 · NHLBI · MAYO CLINIC COLL OF MED, MAYO CLINIC AZ · PI LEE, NANCY A. · 1998 to 2013
$4.2M
Eosinophil-nerve Interactions in Mouse Models of DermatitisR01AR061567 · NIAMS · MAYO CLINIC ARIZONA · PI JACOBSEN, ELIZABETH A, JACOBY, DAVID B · 2012 to 2016
$2.9M
Ozone inhibition of Neuronal m2 receptor functionR01HL055543 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI FRYER, ALLISON DEBORAH · 1996 to 2008
$2.6M
Asthma Exacerbation by Organophosphate PesticidesR01ES014601 · NIEHS · OREGON HEALTH & SCIENCE UNIVERSITY · PI FRYER, ALLISON DEBORAH · 2007 to 2011
$1.7M
Mechanisms of Virus-Induced Hyperreactivity in AtopicsR01HL061013 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOBY, DAVID B · 1998 to 2010
$1.6M
ANTIVIRAL EFFECTS OF EOSINOPHILS IN THE LUNGSR01HL071795 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOBY, DAVID B · 2004 to 2007
$1.5M
Airway Eosinophil Activation by Anticholinergic TherapyR21AI075064 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOBY, DAVID B · 2008 to 2009
$424k
Mouse Models of Eosinophil-Associated Lung DysfunctionR56HL058723 · NHLBI · MAYO CLINIC ARIZONA · PI LEE, NANCY A. · 2008 to 2008
$400k
NCRR NIH HHS RR109709NHLBI NIH HHS HL058723NHLBI NIH HHS HL065228NHLBI NIH HHS HL55543NHLBI NIH HHS HL61013NHLBI NIH HHS HL71795NHLBI NIH HHS R01 HL055543NHLBI NIH HHS R01 HL058723NHLBI NIH HHS R01 HL061013NHLBI NIH HHS R01 HL065228NHLBI NIH HHS R01 HL071795NHLBI NIH HHS R56 HL058723NIAID NIH HHS AI75064NIAID NIH HHS R21 AI075064NIAID NIH HHS T32 AI007472NIAID NIH HHS T32AI007472NIAMS NIH HHS R01 AR061567NIEHS NIH HHS ES14601NIEHS NIH HHS R01 ES014601
6 · The paper itself

Abstract

Cutaneous nerves are increased in atopic dermatitis, and itch is a prominent symptom. We studied the functional interactions between eosinophils and nerves in human and mouse skin and in culture. We demonstrated that human atopic dermatitis skin has eosinophil granule proteins present in the same region as increased nerves. Transgenic mice in which interleukin-5 (IL-5) expression is driven by a keratin-14 (K14) promoter had many eosinophils in the epidermis, and the number of nerves was also significantly increased in the epidermis. In co-cultures, eosinophils dramatically increased branching of sensory neurons isolated from the dorsal root ganglia (DRG) of mice. This effect did not occur in DRG neurons co-cultured with mast cells or with dead eosinophils. Physical contact of the eosinophils with the neurons was not required, and the effect was not blocked by an antibody to nerve growth factor. DRG neurons express eotaxin-1, ICAM-1 and VCAM-1, which may be important in the recruitment, binding, and activation of eosinophils in the region of cutaneous nerves. These data indicate a pathophysiological role for eosinophils in cutaneous nerve growth in atopic dermatitis, and suggest they may present a therapeutic target in atopic dermatitis and other eosinophilic skin conditions with neuronal symptoms such as itch.

Indexed as

AnimalsBiopsyCell CommunicationCell CountCell SurvivalChemokine CCL11Dermatitis, AtopicDermisEosinophil Granule ProteinsEosinophil PeroxidaseEosinophilsEpidermisGanglia, SpinalHealthHumansIntercellular Adhesion Molecule-1Chemokine CCL11Eosinophil Granule ProteinsEosinophil PeroxidaseIntercellular Adhesion Molecule-1Interleukin-5Nerve Growth FactorsVascular Cell Adhesion Molecule-1

Identifiers

PMID21811556
PMCPMC3140999
OpenAlexW2071282917

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Registered trials

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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.