Evidence map›Paper›PMID 35437611›Full record

ArticleCellular and molecular life sciences : CMLS2022

Platelets fine-tune effector responses of naïve CD4

Yanan Min, Long Hao, Xinguang Liu, Shuai Tan, Hui Song, Hao Ni, Zi Sheng, Natalie Jooss, Xuena Liu, Rickard E Malmström and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.7field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 21 citations in OpenAlex.

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  11. The Duality of Collagens in Metastases of Solid Tumors.International journal of molecular sciences · 2025
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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

18 authors at 6 institutions in 2 countries.

Yanan MinDepartment of Medicine-Solna, Cardiovascular Medicine Unit, J8:20, Karolinska Institute, Karolinska University Hospital-Solna, 171 76, Stockholm, Sweden.
Long HaoDepartment of General Surgery, Affiliated Hospital of Jining Medical University, Jining, China.
Xinguang LiuDepartment of Hematology, Qilu Hospital of Shandong University, Jinan, China.
Shuai TanDepartment of Medicine-Solna, Cardiovascular Medicine Unit, J8:20, Karolinska Institute, Karolinska University Hospital-Solna, 171 76, Stockholm, Sweden.
Hui SongDepartment of Clinical Laboratory, Affiliated Hospital of Jining Medical University, Jining, China.
Hao NiDepartment of Medicine-Solna, Cardiovascular Medicine Unit, J8:20, Karolinska Institute, Karolinska University Hospital-Solna, 171 76, Stockholm, Sweden.
Zi ShengDepartment of Hematology, Qilu Hospital of Shandong University, Jinan, China.
Natalie JoossDepartment of Medicine-Solna, Cardiovascular Medicine Unit, J8:20, Karolinska Institute, Karolinska University Hospital-Solna, 171 76, Stockholm, Sweden.
Xuena LiuDepartment of Rheumatology, Qilu Hospital of Shandong University, Jinan, China.
Rickard E MalmströmDepartment of Medicine-Solna, Clinical Epidemiology Unit, Clinical Pharmacology Group, Karolinska Institute, Stockholm, Sweden.
Yang SunSchool of Basic Medicine, Department of Immunology and Shandong University-Karolinska Institutet Collaborative Laboratory, Shandong University Cheeloo Medical College, Jinan, China.
Jianguo LiuShandong First Medical University and Shandong Academy of Medical Science, Institute of Immunology, Taian, China.
Hua TangShandong First Medical University and Shandong Academy of Medical Science, Institute of Immunology, Taian, China.
Hao ZhangDepartment of Hematology, Affiliated Hospital of Jining Medical University, Jining, China.
Chunhong MaSchool of Basic Medicine, Department of Immunology and Shandong University-Karolinska Institutet Collaborative Laboratory, Shandong University Cheeloo Medical College, Jinan, China.
Jun PengDepartment of Hematology, Qilu Hospital of Shandong University, Jinan, China.
Ming HouDepartment of Hematology, Qilu Hospital of Shandong University, Jinan, China.
Nailin LiDepartment of Medicine-Solna, Cardiovascular Medicine Unit, J8:20, Karolinska Institute, Karolinska University Hospital-Solna, 171 76, Stockholm, Sweden. nailin.li@ki.se.ORCID http://orcid.org/0000-0002-3848-7251
Karolinska University Hospital · SEQilu Hospital of Shandong University · CNAffiliated Hospital of Jining Medical University · CNShandong First Medical University · CNShandong University · CNShandong University of Traditional Chinese Medicine · CN

Funding

National Natural Science Foundation of China project no 81700110
6 · The paper itself

Abstract

BACKGROUND AND

aimPlatelets are an able regulator of CD4

methodsPlatelet-Tn cell co-cultures of human cells, genetically modified murine models, and high-throughput bioinformatic analyses were combined to elucidate molecular mechanisms of platelet-dependent regulation.

resultsPlatelets exerted sophisticated regulation on effector responses of type 1, 2, and 17 T helper (Th1/Th2/Th17) and regulatory T (Treg) cells, in time-, concentration-, and organ-dependent manners and with close cooperation of transforming growth factor β (TGFβ) and platelet factor 4 (PF4). PF4 at low concentrations reinforced TGFβ signaling by heteromerizing with type III TGFβ receptor (TGFBRIII), and subsequently enhanced TGFBRII expression and TGFβ signaling. High-concentration PF4 had, however, opposite effects by directly binding to TGFBRII, blocking TGFβ-TGFBRII ligation, and thus inhibiting TGFβ signaling. Furthermore, platelet depletion markedly hampered Treg and Th17 responses in the spleen but not in the lymph nodes, blockade of platelet-Tn cell contact diminished platelet effects, while spleen injection of PF4-immobilized microparticles in PF4-deficient mice mimicked platelet effects, suggesting the importance of direct platelet-Tn contact and platelet-bound PF4 for the optimal regulatory effects by platelets.

conclusionPlatelets exert context-dependent regulations on effector responses of Tn cells via PF4-TGFβ duet, suggesting new possibilities of platelet-targeted interventions of T cell immunity.

Indexed as

Platelet Factor 4Transforming Growth Factor betaAnimalsBlood PlateletsCD4-Positive T-LymphocytesMiceT-Lymphocytes, RegulatoryPlatelet Factor 4Transforming Growth Factor betaEffector cell responsesNaïve CD4+ T cellsPlatelet factor 4PlateletsPlatelet–T cell interactionsTransforming growth factor βType III TGFβ receptorType II TGFβ receptor

Identifiers

PMID35437611
PMCPMC9016031
OpenAlexW4224267697

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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.