Evidence map›Paper›PMID 26110906›Full record

ArticlePloS one2015

The BMP Pathway Participates in Human Naive CD4+ T Cell Activation and Homeostasis.

Víctor G Martínez, Rosa Sacedón, Laura Hidalgo, Jaris Valencia, Lidia M Fernández-Sevilla, Carmen Hernández-López, Angeles Vicente, Alberto Varas

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

28 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
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  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Bone Morphogenetic Proteins Shape TFrontiers in immunology · 2022
    Review
  14. Specific Blockade of Bone Morphogenetic Protein-2/4 Induces Oligodendrogenesis and Remyelination in Demyelinating Disorders.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021
    Article
  15. Article
  16. Review
  17. Article
  18. Inhibition of the BMP Signaling Pathway Ameliorated Established Clinical Symptoms of Experimental Autoimmune Encephalomyelitis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2020
    Article
  19. Article
  20. 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

8 authors at 1 institution in 1 country.

Víctor G MartínezDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Rosa SacedónDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Laura HidalgoDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Jaris ValenciaDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Lidia M Fernández-SevillaDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Carmen Hernández-LópezDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Angeles VicenteDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Alberto VarasDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Universidad Complutense de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone Morphogenetic Proteins (BMPs) form a group of secreted factors that belongs to the TGF-β superfamily. Among different roles in a number of immune cell types, BMPs are known to regulate T cell development within the thymus, although the role of BMP signaling in human mature T cells remains elusive. In this study, we demonstrate that canonical BMP signaling is necessary during two critical events that regulate the size and function of human naive CD4+ T cell population: activation and homeostasis. Upon stimulation via TCR, naive CD4+ T cells upregulate the expression of BMP ligands triggering canonical BMP signaling in CD25+ cells. Blockade of BMP signaling severely impairs CD4+ T cell proliferation after activation mainly through regulation of IL-2, since the addition of this cytokine recuperates normal T cell expansion after inhibition of BMP signaling. Similarly, activation of canonical BMP pathway is required for both the maintenance of cell survival and the homeostatic proliferation induced by IL-7, a key factor for T cell homeostasis. Moreover, upregulation of two critical receptors for T cell homeostasis, CXCR4 and CCR9, triggered by IL-7 is also abrogated in the absence of BMP signaling. Collectively, we describe important roles of the canonical BMP signaling in human naive CD4+ T cell activation and homeostasis that could be valuable for clinical application.

Indexed as

Activin Receptors, Type IIApoptosisBone Morphogenetic Protein Receptors, Type IBone Morphogenetic ProteinsCD4-Positive T-LymphocytesCell DifferentiationCell ProliferationCells, CulturedGene Expression RegulationHumansInterleukin-2Interleukin-7Lymphocyte ActivationActivin Receptors, Type IIACVRL1 protein, humanBone Morphogenetic Protein Receptors, Type IBone Morphogenetic ProteinsIL2 protein, humanIL7 protein, humanInterleukin-2Interleukin-7

Identifiers

PMID26110906
PMCPMC4481406
OpenAlexW1923387937

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.