Evidence map›Paper›PMID 34255742›Full record

ArticleJCI insight2021

CD40L modulates transcriptional signatures of neutrophils in the bone marrow associated with development and trafficking.

Tábata Takahashi França, Ashraf Al-Sbiei, Ghada Bashir, Yassir Awad Mohamed, Ranieri Coelho Salgado, Lucila Akune Barreiros, Sarah Maria da Silva Napoleão, Cristina Worm Weber, Janaíra Fernandes Severo Ferreira, Carolina Sanchez Aranda and 8 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Inhibition of IP6K1 suppresses NPA formation via platelet short-chain polyphosphate polymers in necrotizing enterocolitis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
  2. Article
  3. Review
  4. CD40 Ligand Potentiates Immunogenecity ofCurrent issues in molecular biology · 2025
    Article
  5. Article
  6. Article
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

18 authors at 10 institutions in 7 countries.

Tábata Takahashi FrançaDepartment of Immunology, Institute of Biomedical Science, University of São Paulo, São Paulo, São Paulo, Brazil.
Ashraf Al-SbieiDepartment of Medical Microbiology and Immunology, College of Medicine and Health Sciences, United Arab Emirates (UAE) University, Al Ain, Abu Dhabi, United Arab Emirates.
Ghada BashirDepartment of Medical Microbiology and Immunology, College of Medicine and Health Sciences, United Arab Emirates (UAE) University, Al Ain, Abu Dhabi, United Arab Emirates.
Yassir Awad MohamedDepartment of Medical Microbiology and Immunology, College of Medicine and Health Sciences, United Arab Emirates (UAE) University, Al Ain, Abu Dhabi, United Arab Emirates.
Ranieri Coelho SalgadoDepartment of Immunology, Institute of Biomedical Science, University of São Paulo, São Paulo, São Paulo, Brazil.
Lucila Akune BarreirosDepartment of Immunology, Institute of Biomedical Science, University of São Paulo, São Paulo, São Paulo, Brazil.
Sarah Maria da Silva NapoleãoDepartment of Immunology, Institute of Biomedical Science, University of São Paulo, São Paulo, São Paulo, Brazil.
Cristina Worm WeberPediatric Allergy & Immunology Clinic, Caxias do Sul, Rio Grande do Sul, Brazil.
Janaíra Fernandes Severo FerreiraAlbert Sabin Hospital, Fortaleza, Ceará, Brazil.
Carolina Sanchez ArandaDivision of Allergy, Immunology, and Rheumatology, Department of Pediatrics, Federal University of São Paulo, São Paulo, São Paulo, Brazil.
Carolina PrandoFaculdades Pequeno Príncipe, Pelé Pequeno Principe Research Intitute, Curitiba, Paraná, Brazil.
Mayra B de Barros DornaDivision of Allergy and Immunology, Department of Pediatrics, Children's Institute, Hospital das Clínicas, São Paulo, São Paulo, Brazil.
Igor JurisicaOsteoarthritis Research Program, Division of Orthopedic Surgery, Schroeder Arthritis Institute, University Health Network, Krembil Research Institute, University Health Network, Departments of Medical Biophysics and Computer Science, University of Toronto, Toronto, Ontaro, Canada.
Maria J Fernandez-CabezudoDepartment of Biochemistry and Molecular Biology, College of Medicine and Health Sciences, UAE University, Al Ain, Abu Dhabi, United Arab Emirates.
Hans D OchsDepartment of Pediatrics, University of Washington School of Medicine, and Seattle Children's Research Institute, Seattle, Washington, USA.
Antonio Condino-NetoDepartment of Immunology, Institute of Biomedical Science, University of São Paulo, São Paulo, São Paulo, Brazil.
Basel K Al-RamadiDepartment of Medical Microbiology and Immunology, College of Medicine and Health Sciences, United Arab Emirates (UAE) University, Al Ain, Abu Dhabi, United Arab Emirates.
Otavio Cabral-MarquesDepartment of Immunology, Institute of Biomedical Science, University of São Paulo, São Paulo, São Paulo, Brazil.
Institute of Biomedical Science · GBUnited Arab Emirates University · AECentro Universitário Franciscano do Paraná · BRHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRHospital Infantil Albert Sabin · BRSeattle Children's Hospital · USUniversidade de Caxias do Sul · BRUniversidade de São Paulo · BRUniversidade Federal de São Paulo · BRUniversity Health Network · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutrophils are produced in the BM in a process called granulopoiesis, in which progenitor cells sequentially develop into mature neutrophils. During the developmental process, which is finely regulated by distinct transcription factors, neutrophils acquire the ability to exit the BM, properly distribute throughout the body, and migrate to infection sites. Previous studies have demonstrated that CD40 ligand (CD40L) influences hematopoiesis and granulopoiesis. Here, we investigate the effect of CD40L on neutrophil development and trafficking by performing functional and transcriptome analyses. We found that CD40L signaling plays an essential role in the early stages of neutrophil generation and development in the BM. Moreover, CD40L modulates transcriptional signatures, indicating that this molecule enables neutrophils to traffic throughout the body and to migrate in response to inflammatory signals. Thus, our study provides insights into the complex relationships between CD40L signaling and granulopoiesis, and it suggests a potentially novel and nonredundant role of CD40L signaling in neutrophil development and function.

Indexed as

AnimalsBone MarrowCD40 AntigensCD40 LigandCell DifferentiationCell MovementCells, CulturedFemaleGene Expression Regulation, DevelopmentalHematopoiesisMiceMice, KnockoutModels, AnimalNeutrophilsRNA-SeqSignal TransductionCD40 AntigensCD40 LigandBone marrow differentiationCell BiologyImmunologyNeutrophils

Identifiers

PMID34255742
PMCPMC8410015
OpenAlexW3178154641

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.