Evidence map›Paper›PMID 35830602›Full record

ArticleMolecular biology of the cell2022

Nanotopography modulates cytoskeletal organization and dynamics during T cell activation.

Brittany A Wheatley, Ivan Rey-Suarez, Matt J Hourwitz, Sarah Kerr, Hari Shroff, John T Fourkas, Arpita Upadhyaya

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. CD4International journal of molecular sciences · 2025
    Article
  3. Dynamic Plasma Membrane Topography Linked With Arp2/3 Actin Network Induction During Cell Shape Change.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
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

7 authors at 4 institutions in 1 country.

Brittany A WheatleyDepartment of Integrative Structural and Computational Biology and.
Ivan Rey-SuarezInstitute for Physical Science and Technology, University of Maryland, College Park, MD 20742.
Matt J HourwitzDepartment of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742.
Sarah KerrDepartment of Physics, University of Colorado, Boulder, CO 80302.
Hari ShroffNational Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD 20892.
John T FourkasInstitute for Physical Science and Technology, University of Maryland, College Park, MD 20742.
Arpita UpadhyayaInstitute for Physical Science and Technology, University of Maryland, College Park, MD 20742.
University of Maryland, College Park · USNational Institutes of Health · USScripps Research Institute · USUniversity of Colorado Boulder · US

Funding

Section on High Resolution Optical ImagingZIAEB000074 · NIBIB · NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING · PI SHROFF, HARI · 2010 to 2022
$15.2M
Supplement request for Microtubule regulation of actomyosin dynamics and force generation in T lymphocytesR01GM131054 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI UPADHYAYA, ARPITA · 2019 to 2022
$1.4M
NIGMS NIH HHS R01 GM131054
6 · The paper itself

Abstract

Exposure to MHC-antigen complexes on the surface of antigen-presenting cells (APCs) activates T cells, inducing the formation of the immune synapse (IS). Antigen detection at the APC surface is thus a critical step in the adaptive immune response. The physical properties of antigen-presenting surfaces encountered by T cells in vivo are believed to modulate T cell activation and proliferation. Although stiffness and ligand mobility influence IS formation, the effect of the complex topography of the APC surface on this process is not well understood. Here we investigate how nanotopography modulates cytoskeletal dynamics and signaling during the early stages of T cell activation using high-resolution fluorescence microscopy on nanofabricated surfaces with parallel nanoridges of different spacings. We find that although nanoridges reduce the maximum spread area as compared with cells on flat surfaces, the ridges enhance the accumulation of actin and the signaling kinase ZAP-70 at the IS. Actin polymerization is more dynamic in the presence of ridges, which influence the directionality of both actin flows and microtubule (MT) growth. Our results demonstrate that the topography of the activating surface exerts both global effects on T cell morphology and local changes in actin and MT dynamics, collectively influencing T cell signaling.

Indexed as

ActinsLymphocyte ActivationAntigen-Presenting CellsCytoskeletonT-LymphocytesActins

Identifiers

PMID35830602
PMCPMC9582624
OpenAlexW4285496640

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.