Evidence map›Paper›PMID 38532626›Full record

ArticleBiophysical journal2024

Increased vesicular dynamics and nanoscale clustering of IL-2 after T cell activation.

Badeia Saed, Neal T Ramseier, Thilini Perera, Jesse Anderson, Jacob Burnett, Hirushi Gunasekara, Alyssa Burgess, Haoran Jing, Ying S Hu

Open access · greenAbstract read
In one paragraph

Article in Biophysical journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Biophysics of immune cell signaling.Biophysical journal · 2024
    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

9 authors at 3 institutions in 1 country.

Badeia SaedDepartment of Chemistry, College of Liberal Arts and Sciences, University of Illinois Chicago, Chicago, Illinois.
Neal T RamseierDepartment of Chemistry, College of Liberal Arts and Sciences, University of Illinois Chicago, Chicago, Illinois.
Thilini PereraDepartment of Chemistry, College of Liberal Arts and Sciences, University of Illinois Chicago, Chicago, Illinois.
Jesse AndersonDepartment of Chemical Engineering, College of Engineering, University of Illinois Chicago, Chicago, Illinois.
Jacob BurnettNikon Instruments Inc, Melville, New York.
Hirushi GunasekaraDepartment of Chemistry, College of Liberal Arts and Sciences, University of Illinois Chicago, Chicago, Illinois.
Alyssa BurgessDepartment of Chemistry, College of Liberal Arts and Sciences, University of Illinois Chicago, Chicago, Illinois.
Haoran JingDepartment of Chemistry, College of Liberal Arts and Sciences, University of Illinois Chicago, Chicago, Illinois.
Ying S HuDepartment of Chemistry, College of Liberal Arts and Sciences, University of Illinois Chicago, Chicago, Illinois. Electronic address: yshu@uic.edu.
University of Illinois Chicago · USIllinois College · USNikon (United States) · US

Funding

Ultrasensitive quantification of cytokine release from T cellsR35GM146786 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Ying Samuel Hu · 2022 to 2026
$2.2M
NIGMS NIH HHS R35 GM146786
6 · The paper itself

Abstract

T cells coordinate intercellular communication through the meticulous regulation of cytokine secretion. Direct visualization of vesicular transport and intracellular distribution of cytokines provides valuable insights into the temporal and spatial mechanisms involved in regulation. Employing Jurkat E6-1 T cells and interleukin-2 (IL-2) as a model system, we investigated vesicular dynamics using single-particle tracking and the nanoscale distribution of intracellular IL-2 in fixed T cells using superresolution microscopy. Live-cell imaging revealed that in vitro activation resulted in increased vesicular dynamics. Direct stochastic optical reconstruction microscopy and 3D structured illumination microscopy revealed nanoscale clustering of IL-2. In vitro activation correlated with spatial accumulation of IL-2 nanoclusters into more pronounced and elongated clusters. These observations provide visual evidence that accelerated vesicular transport and spatial concatenation of IL-2 clusters at the nanoscale may constitute a potential mechanism for modulating cytokine release by Jurkat T cells.

Indexed as

Interleukin-2Lymphocyte ActivationT-LymphocytesHumansJurkat CellsInterleukin-2

Identifiers

PMID38532626
PMCPMC11331045
OpenAlexW4393195515

What Socratic holds

Textmetadata
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 Socratic graph.