Evidence map›Paper›PMID 32601597›Full record

ArticleFrontiers in physics2019

T-Cell Mechanobiology: Force Sensation, Potentiation, and Translation.

Devin L Harrison, Yun Fang, Jun Huang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

45 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Biomaterial-EnabledCell biomaterials · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Acute priming using elevated fluid viscosity recovers 'bioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Mechanical force matters in early T cell activation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  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

3 authors at 1 institution in 1 country.

Devin L HarrisonThe Graduate Program in Biophysical Sciences, The University of Chicago, Chicago, IL, United States.
Yun FangThe Graduate Program in Biophysical Sciences, The University of Chicago, Chicago, IL, United States.
Jun HuangThe Graduate Program in Biophysical Sciences, The University of Chicago, Chicago, IL, United States.
University of Chicago · US

Funding

MULTIDISCIPLINARY CARDIAC SCIENCEST32HL007381 · NHLBI · UNIVERSITY OF CHICAGO · PI JEANNE M DECARA, Yoav Gilad · 1985 to 2026
$12.5M
Graduate Program in Biophysical Sciences at the University of Chicago - Renewal 0T32EB009412 · NIBIB · UNIVERSITY OF CHICAGO · PI ENGEL, GREGORY S, SOSNICK, TOBIN R · 2009 to 2023
$4.9M
Molecular mechanism of natural killer cell recognitionDP2AI144245 · NIAID · UNIVERSITY OF CHICAGO · PI HUANG, JUN · 2018 to 2022
$2.9M
Coronary artery disease locus 1p32.2 and miR92a-PPAP2B signaling in endothelial mechanobiologyR01HL136765 · NHLBI · UNIVERSITY OF CHICAGO · PI FANG, YUN · 2017 to 2021
$2.0M
Spatial Delivery of MicroRNA Inhibitor via Targeted Polyelectrolyte Complex Micelles to Treat Atherosclerosis.R01HL138223 · NHLBI · UNIVERSITY OF CHICAGO · PI FANG, YUN · 2017 to 2021
$2.0M
Recognition of cross-reactive antigens by human CD4+ T cellsR00AI106941 · NIAID · UNIVERSITY OF CHICAGO · PI HUANG, JUN · 2015 to 2016
$497k
Direct visualization of serial engagement by T cell receptorsR21AI120010 · NIAID · UNIVERSITY OF CHICAGO · PI HUANG, JUN · 2015 to 2016
$425k
NHLBI NIH HHS R01 HL136765NHLBI NIH HHS R01 HL138223NHLBI NIH HHS T32 HL007381NIAID NIH HHS DP2 AI144245NIAID NIH HHS R00 AI106941NIAID NIH HHS R21 AI120010NIBIB NIH HHS T32 EB009412
6 · The paper itself

Abstract

A T cell is a sensitive self-referential mechanical sensor. Mechanical forces influence the recognition, activation, differentiation, and function throughout the lifetime of a T cell. T cells constantly perceive and respond to physical stimuli through their surface receptors, cytoskeleton, and subcellular structures. Surface receptors receive physical cues in the form of forces generated through receptor-ligand binding events, which are dynamically regulated by contact tension, shear stress, and substrate rigidity. The resulting mechanotransduction not only influences T-cell recognition and signaling but also possibly modulates cell metabolism and gene expression. Moreover, forces also dynamically regulate the deformation, organization, and translocation of cytoskeleton and subcellular structures, leading to changes in T-cell mobility, migration, and infiltration. However, the roles and mechanisms of how mechanical forces modulate T-cell recognition, signaling, metabolism, and gene expression, are largely unknown and underappreciated. Here, we review recent technological and scientific advances in T-cell mechanobiology, discuss possible roles and mechanisms of T-cell mechanotransduction, and propose new research directions of this emerging field in health and disease.

Indexed as

forcemechanotransductionmetabolismreceptor-ligand interactionT cellT-cell activationT-cell differentiationT-cell recognition

Identifiers

PMID32601597
PMCPMC7323161
OpenAlexW2933229048

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.