Evidence map›Paper›PMID 36493773›Full record

ArticleDevelopmental cell2022

Langerhans cells are essential components of the angiogenic niche during murine skin repair.

Renee Wasko, Kate Bridges, Rebecca Pannone, Ikjot Sidhu, Yue Xing, Shruti Naik, Kathryn Miller-Jensen, Valerie Horsley

Open access · greenAbstract read
In one paragraph

Article in Developmental cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.8field-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

31 citing papers in PubMed, 49 citations in OpenAlex.

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  19. Transcriptional analysis of efferocytosis in mouse skin wounds.bioRxiv : the preprint server for biology · 2024
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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

8 authors at 2 institutions in 1 country.

Renee WaskoDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, USA.
Kate BridgesDepartment of Biomedical Engineering, Yale University, New Haven, CT, USA.
Rebecca PannoneDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, USA.
Ikjot SidhuDepartment of Pathology, NYU Langone Health, New York, NY, USA.
Yue XingDepartment of Pathology, NYU Langone Health, New York, NY, USA.
Shruti NaikDepartment of Pathology, NYU Langone Health, New York, NY, USA.
Kathryn Miller-JensenDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, USA; Department of Biomedical Engineering, Yale University, New Haven, CT, USA. Electronic address: kathryn.miller-jensen@yale.edu.
Valerie HorsleyDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, USA; Department of Dermatology, Yale School of Medicine, New Haven, CT, USA. Electronic address: valerie.horsley@yale.edu.
Yale University · USNYU Langone Health · US

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007499 · NIGMS · YALE UNIVERSITY · PI CARLSON, JOHN R, REINKE, VALERIE J · 1985 to 2022
$13.9M
Structure of the HIV-1 GenomeR01AI068462 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WEEKS, KEVIN M · 2006 to 2020
$7.4M
Systems analysis of cell-cell communication networks and immune activity in the melanoma tumor microenvironmentU01CA238728 · NCI · YALE UNIVERSITY · PI BOSENBERG, MARCUS W, MILLER-JENSEN, KATHRYN · 2020 to 2024
$2.9M
Systems analysis of cell-to-cell variability and signaling-transcription factor motifs regulating macrophage responses to conflicting environmental cuesR01GM123011 · NIGMS · YALE UNIVERSITY · PI MILLER-JENSEN, KATHRYN · 2017 to 2025
$2.5M
Defining the role of lymphatic vessels in wound healingR01AR079232 · NIAMS · YALE UNIVERSITY · PI HORSLEY, VALERIE · 2021 to 2025
$2.5M
Mechanism and Impact of Dermal adipocyte remodeling in skin fibrosisR01AR076938 · NIAMS · YALE UNIVERSITY · PI ATIT, RADHIKA P, HORSLEY, VALERIE · 2020 to 2024
$2.4M
Adipocyte lipolysis regulates skin repairR01AR075412 · NIAMS · YALE UNIVERSITY · PI HORSLEY, VALERIE · 2019 to 2023
$2.3M
Dissecting the contributions of Langerhans cell to cutaneous wound healingF31AR073094 · NIAMS · YALE UNIVERSITY · PI WASKO, RENEE · 2019 to 2021
$137k
NCI NIH HHS U01 CA238728NIAID NIH HHS R01 AI068462NIAMS NIH HHS F31 AR073094NIAMS NIH HHS R01 AR075412NIAMS NIH HHS R01 AR076938NIAMS NIH HHS R01 AR079232NIGMS NIH HHS R01 GM123011NIGMS NIH HHS T32 GM007499
6 · The paper itself

Abstract

Angiogenesis, the growth of new blood vessels from pre-existing vessels, occurs during development, injury repair, and tumorigenesis to deliver oxygen, immune cells, and nutrients to tissues. Defects in angiogenesis occur in cardiovascular and inflammatory diseases, and chronic, non-healing wounds, yet treatment options are limited. Here, we provide a map of the early angiogenic niche by analyzing single-cell RNA sequencing of mouse skin wound healing. Our data implicate Langerhans cells (LCs), phagocytic, skin-resident immune cells, in driving angiogenesis during skin repair. Using lineage-driven reportersw, three-dimensional (3D) microscopy, and mouse genetics, we show that LCs are situated at the endothelial cell leading edge in mouse skin wounds and are necessary for angiogenesis during repair. These data provide additional future avenues for the control of angiogenesis to treat disease and chronic wounds and extend the function of LCs beyond their canonical role in antigen presentation and T cell immunity.

Indexed as

Langerhans CellsWound HealingAnimalsMiceNeovascularization, PhysiologicSkinangiogenesisEndothelial cellsLangerhans cellssingle-cell RNA sequencingskintissue repairwound healing

Identifiers

PMID36493773
PMCPMC10848275
OpenAlexW4312094010

What OpenQuestion holds

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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.