Evidence map›Paper›PMID 32457763›Full record

ArticleFrontiers in immunology2020

Smad2/4 Signaling Pathway Is Critical for Epidermal Langerhans Cell Repopulation Under Inflammatory Condition but Not Required for Their Homeostasis at Steady State.

Linting Huang, Gui-Hua Li, Qian Yu, Yingping Xu, Steven Cvetkovski, Xuan Wang, Nirmal Parajuli, Imo Udo-Inyang, Daniel Kaplan, Li Zhou and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. The roles of tissue resident macrophages in health and cancer.Experimental hematology & oncology · 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

12 authors at 3 institutions in 2 countries.

Linting HuangDepartment of Dermatology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Gui-Hua LiCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health System, Detroit, MI, United States.
Qian YuCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health System, Detroit, MI, United States.
Yingping XuCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health System, Detroit, MI, United States.
Steven CvetkovskiCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health System, Detroit, MI, United States.
Xuan WangCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health System, Detroit, MI, United States.
Nirmal ParajuliCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health System, Detroit, MI, United States.
Imo Udo-InyangCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health System, Detroit, MI, United States.
Daniel KaplanDepartment of Dermatology, University of Pittsburgh, Pittsburgh, PA, United States.
Li ZhouCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health System, Detroit, MI, United States.
Zhirong YaoDepartment of Dermatology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Qing-Sheng MiCenter for Cutaneous Biology and Immunology, Department of Dermatology, Henry Ford Health System, Detroit, MI, United States.
Henry Ford Health System · USShanghai Jiao Tong University · CNUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidermal Langerhans cells (LCs) are skin-resident dendritic cells that are essential for the induction of skin immunity and tolerance. Transforming growth factor-β 1 (TGFβ1) is a crucial factor for LC maintenance and function. However, the underlying TGFβ1 signaling pathways remain unclear. Our previous research has shown that the TGFβ1/Smad3 signaling pathway does not impact LC homeostasis and maturation. In this study, we generated mice with conditional deletions of either individual Smad2, Smad4, or both Smad2 and Smad4 in the LC lineage or myeloid lineage, to further explore the impact of TGFβ1/Smad signaling pathways on LCs. We found that interruption of Smad2 or Smad4 individually or simultaneously in the LC lineage did not significantly impact the maintenance, maturation, antigen uptake, and migration of LCs

Indexed as

Cell ProliferationAnimalsBone Marrow CellsCell LineageCell MovementCells, CulturedDermatitisDisease Models, AnimalEpidermisFemaleLangerhans CellsLymph NodesMaleMice, Inbred C57BLMice, KnockoutPhagocytosisCsf1r protein, mouseReceptors, Granulocyte-Macrophage Colony-Stimulating FactorSmad2 ProteinSmad2 protein, mouseSmad4 ProteinSmad4 protein, mouseTgfb1 protein, mouseTransforming Growth Factor beta1Langerhans cellsSmad2Smad3Smad4transforming growth factor-β1

Identifiers

PMID32457763
PMCPMC7221176
OpenAlexW3023209657

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.