Evidence map›Paper›PMID 31971954›Full record

ArticlePloS one2020

Tissue-resident macrophages can be generated de novo in adult human skin from resident progenitor cells during substance P-mediated neurogenic inflammation ex vivo.

Jennifer Gherardini, Youhei Uchida, Jonathan A Hardman, Jérémy Chéret, Kimberly Mace, Marta Bertolini, Ralf Paus

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. A Bispecific, Tetravalent Antibody Targeting Inflammatory and Pruritogenic Pathways in Atopic Dermatitis.JID innovations : skin science from molecules to population health · 2024
    Article
  8. Review
  9. Review
  10. Tissue-Resident Immune Cells in Humans.Annual review of immunology · 2022
    Review
  11. Review
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 4 institutions in 4 countries.

Jennifer GherardiniMonasterium Laboratory GmbH, Münster, Germany.ORCID 0000-0002-4811-8580
Youhei UchidaDepartment of Dermatology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Jonathan A HardmanCentre for Dermatology Research and NIHR Manchester Biomedical Research Centre University of Manchester, Manchester, United Kingdom.ORCID 0000-0002-1653-7908
Jérémy ChéretDr. Phillip Frost Department of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, Florida, United States of America.
Kimberly MaceDivision of Cell Matrix Biology and Regenerative Medicine, University of Manchester, Manchester, United Kingdom.ORCID 0000-0002-3184-878X
Marta BertoliniMonasterium Laboratory GmbH, Münster, Germany.
Ralf PausMonasterium Laboratory GmbH, Münster, Germany.
Monasterium Laboratory Skin & Hair Research Solutions (Germany) · DEUniversity of Manchester · GBUniversity of Miami · USKagoshima University · JP

Funding

Department of Health
6 · The paper itself

Abstract

Besides monocyte (MO)-derived macrophages (MACs), self-renewing tissue-resident macrophages (trMACs) maintain the intracutaneous MAC pool in murine skin. Here, we have asked whether the same phenomenon occurs in human skin using organ-cultured, full-thickness skin detached from blood circulation and bone marrow. Skin stimulation ex vivo with the neuropeptide substance P (SP), mimicking neurogenic skin inflammation, significantly increased the number of CD68+MACs in the papillary dermis without altering intracutaneous MAC proliferation or apoptosis. Since intraluminal CD14+MOs were undetectable in the non-perfused dermal vasculature, new MACs must have differentiated from resident intracutaneous progenitor cells in human skin. Interestingly, CD68+MACs were often seen in direct cell-cell-contact with cells expressing both, the hematopoietic stem cell marker CD34 and SP receptor (neurokinin-1 receptor [NK1R]). These cell-cell contacts and CD34+cell proliferation were up-regulated in SP-treated skin samples. Collectively, our study provides the first evidence that resident MAC progenitors, from which mature MACs can rapidly differentiate within the tissue, do exist in normal adult human skin. That these NK1R+trMAC-progenitor cells quickly respond to a key stress-associated neuroinflammatory stimulus suggests that this may satisfy increased local MAC demand under conditions of wounding/stress.

Indexed as

AdultAntigens, CDAntigens, CD34Antigens, Differentiation, MyelomonocyticApoptosisCD68 MoleculeCell DifferentiationFemaleHumansMacrophagesNeurogenic InflammationOrgan Culture TechniquesSkinStem CellsSubstance PAntigens, CDAntigens, CD34Antigens, Differentiation, MyelomonocyticCD68 antigen, humanCD68 MoleculeSubstance P

Identifiers

PMID31971954
PMCPMC6977738
OpenAlexW3001279661

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.