Evidence map›Paper›PMID 34172580›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

Molecular design of the γδT cell receptor ectodomain encodes biologically fit ligand recognition in the absence of mechanosensing.

Robert J Mallis, Jonathan S Duke-Cohan, Dibyendu Kumar Das, Aoi Akitsu, Adrienne M Luoma, Debasis Banik, Hannah M Stephens, Paul W Tetteh, Caitlin D Castro, Sophie Krahnke and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Development of αβ and γδ T Cells in the Thymus and Methods of Analysis.International journal of molecular sciences · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Cancer immunotherapy by γδ T cells.Science (New York, N.Y.) · 2024
    Review
  11. Article
  12. Article
  13. Mechanical force matters in early T cell activation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  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

18 authors at 6 institutions in 3 countries.

Robert J MallisLaboratory of Immunobiology, Dana-Farber Cancer Institute, Boston, MA 02115.ORCID 0000-0002-2087-9468
Jonathan S Duke-CohanLaboratory of Immunobiology, Dana-Farber Cancer Institute, Boston, MA 02115.ORCID 0000-0002-9478-9609
Dibyendu Kumar DasDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN 37235.
Aoi AkitsuLaboratory of Immunobiology, Dana-Farber Cancer Institute, Boston, MA 02115.
Adrienne M LuomaDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637.
Debasis BanikDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN 37235.ORCID 0000-0003-1065-991X
Hannah M StephensDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN 37235.ORCID 0000-0002-9191-0303
Paul W TettehLaboratory of Immunobiology, Dana-Farber Cancer Institute, Boston, MA 02115.ORCID 0000-0003-4381-498X
Caitlin D CastroDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637.
Sophie KrahnkeDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637.
Rebecca E HusseyLaboratory of Immunobiology, Dana-Farber Cancer Institute, Boston, MA 02115.ORCID 0000-0002-8870-4111
Brian LawneyDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115.
Kristine N BrazinLaboratory of Immunobiology, Dana-Farber Cancer Institute, Boston, MA 02115.
Pedro A RecheDepartment of Immunology, Faculty of Medicine, Universidad Complutense de Madrid, 28040 Madrid, Spain.ORCID 0000-0003-3966-5838
Wonmuk HwangDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843; hwm@tamu.edu ejadams@uchicago.edu matt.lang@vanderbilt.edu ellis_reinherz@dfci.harvard.edu.ORCID 0000-0001-7514-3186
Erin J AdamsDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637; hwm@tamu.edu ejadams@uchicago.edu matt.lang@vanderbilt.edu ellis_reinherz@dfci.harvard.edu.ORCID 0000-0002-6271-8574
Matthew J LangDepartment of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN 37235; hwm@tamu.edu ejadams@uchicago.edu matt.lang@vanderbilt.edu ellis_reinherz@dfci.harvard.edu.ORCID 0000-0002-8198-144X
Ellis L ReinherzLaboratory of Immunobiology, Dana-Farber Cancer Institute, Boston, MA 02115; hwm@tamu.edu ejadams@uchicago.edu matt.lang@vanderbilt.edu ellis_reinherz@dfci.harvard.edu.ORCID 0000-0003-1048-5526
Harvard University · USUniversity of Chicago · USVanderbilt University · USDana-Farber Cancer Institute · USKorea Institute for Advanced Study · KRUniversidad Complutense de Madrid · ES

Funding

Protein Production CoreP01AI143565 · NIAID · DANA-FARBER CANCER INST · PI ELLIS L REINHERZ · 2020 to 2026
$19.9M
Understanding the structural basis of T cell receptor (TCR) and preTCR mechanosensing: single molecule, NMR and molecular dynamics studiesR01AI136301 · NIAID · VANDERBILT UNIVERSITY · PI LANG, MATTHEW J. · 2018 to 2022
$3.9M
Molecular Recognition of Ligand by the Gamma Delta T Cell ReceptorR01AI073922 · NIAID · UNIVERSITY OF CHICAGO · PI ADAMS, ERIN JUNE · 2007 to 2016
$3.8M
Thymocyte integrin regulation by plexinD1R01AI115698 · NIAID · DANA-FARBER CANCER INST · PI REINHERZ, ELLIS L · 2015 to 2018
$1.7M
NIAID NIH HHS P01 AI143565NIAID NIH HHS R01 AI073922NIAID NIH HHS R01 AI115698NIAID NIH HHS R01 AI136301
6 · The paper itself

Abstract

High-acuity αβT cell receptor (TCR) recognition of peptides bound to major histocompatibility complex molecules (pMHCs) requires mechanosensing, a process whereby piconewton (pN) bioforces exert physical load on αβTCR-pMHC bonds to dynamically alter their lifetimes and foster digital sensitivity cellular signaling. While mechanotransduction is operative for both αβTCRs and pre-TCRs within the αβT lineage, its role in γδT cells is unknown. Here, we show that the human DP10.7 γδTCR specific for the sulfoglycolipid sulfatide bound to CD1d only sustains a significant load and undergoes force-induced structural transitions when the binding interface-distal γδ constant domain (C) module is replaced with that of αβ. The chimeric γδ-αβTCR also signals more robustly than does the wild-type (WT) γδTCR, as revealed by RNA-sequencing (RNA-seq) analysis of TCR-transduced

Indexed as

Mechanotransduction, CellularAmino Acid SequenceAnimalsGene Expression ProfilingHumansLigandsMiceProtein DomainsProtein StabilityProtein Structure, SecondaryReceptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-deltaSignal TransductionSingle Molecule ImagingThymocytesThymus GlandLigandsReceptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-deltamechanosensoroptical tweezersT cell activationT cell receptorγδT cells

Identifiers

PMID34172580
PMCPMC8256041
OpenAlexW3175444873

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.