Evidence map›Paper›PMID 25494999›Full record

ArticleBMC immunology2014

Lipid raft-based membrane order is important for antigen-specific clonal expansion of CD4(+) T lymphocytes.

Daniel Schieffer, Sanya Naware, Walter Bakun, Anil K Bamezai

Open access · goldAbstract read
In one paragraph

Article in BMC immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

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  13. Effects of Omega-3 Fatty Acids on Immune Cells.International journal of molecular sciences · 2019
    Review
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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

4 authors at 1 institution in 1 country.

Daniel SchiefferDepartment of Biology, Villanova University, 800 Lancaster Avenue, Villanova, PA, 19085, USA. schiefda@gmail.com.
Sanya NawareDepartment of Biology, Villanova University, 800 Lancaster Avenue, Villanova, PA, 19085, USA. Sanya.naware@gmail.com.
Walter BakunDepartment of Biology, Villanova University, 800 Lancaster Avenue, Villanova, PA, 19085, USA. wbakun@villanova.edu.
Anil K BamezaiDepartment of Biology, Villanova University, 800 Lancaster Avenue, Villanova, PA, 19085, USA. anil.bamezai@villanova.edu.
Villanova University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLipid rafts are cholesterol and saturated lipid-rich, nanometer sized membrane domains that are hypothesized to play an important role in compartmentalization and spatiotemporal regulation of cellular signaling. Lipid rafts contribute to the plasma membrane order and to its spatial asymmetry, as well. The raft nanodomains on the surface of CD4(+) T lymphocytes coalesce during their interaction with antigen presenting cells (APCs). Sensing of foreign antigen by the antigen receptor on CD4(+) T cells occurs during these cell-cell interactions. In response to foreign antigen the CD4(+) T cells proliferate, allowing the expansion of few antigen-specific primary CD4(+) T cell clones. Proliferating CD4(+) T cells specialize in their function by undergoing differentiation into appropriate effectors tailored to mount an effective adaptive immune response against the invading pathogen.

resultsTo investigate the role of lipid raft-based membrane order in the clonal expansion phase of primary CD4(+) T cells, we have disrupted membrane order by incorporating an oxysterol, 7-ketocholesterol (7-KC), into the plasma membrane of primary CD4(+) T cells expressing a T cell receptor specific to chicken ovalbumin323-339 peptide sequence and tested their antigen-specific response. We report that 7-KC, at concentrations that disrupt lipid rafts, significantly diminish the c-Ovalbumin323-339 peptide-specific clonal expansion of primary CD4(+) T cells.

conclusionsOur findings suggest that lipid raft-based membrane order is important for clonal expansion of CD4(+) T cells in response to a model peptide.

Indexed as

Cell ProliferationAnimalsAntigensCD4-Positive T-LymphocytesGene Expression RegulationMembrane MicrodomainsMiceMice, TransgenicReceptors, Antigen, T-CellAntigensReceptors, Antigen, T-Cell

Identifiers

PMID25494999
PMCPMC4270042
OpenAlexW1973309243

What OpenQuestion holds

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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.