Evidence map›Paper›PMID 38077328›Full record

ArticleFrontiers in immunology2023

The Rac-GEF Tiam1 controls integrin-dependent neutrophil responses.

Kirsti Hornigold, Martin J Baker, Polly A Machin, Stephen A Chetwynd, Anna-Karin Johnsson, Chiara Pantarelli, Priota Islam, Melanie Stammers, Laraine Crossland, David Oxley and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. 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

17 authors at 3 institutions in 2 countries.

Kirsti Hornigold *Signalling Programme, Babraham Institute, Cambridge, United Kingdom.
Martin J Baker *Signalling Programme, Babraham Institute, Cambridge, United Kingdom.
Polly A Machin *Signalling Programme, Babraham Institute, Cambridge, United Kingdom.
Stephen A ChetwyndSignalling Programme, Babraham Institute, Cambridge, United Kingdom.
Anna-Karin JohnssonSignalling Programme, Babraham Institute, Cambridge, United Kingdom.
Chiara PantarelliSignalling Programme, Babraham Institute, Cambridge, United Kingdom.
Priota IslamSignalling Programme, Babraham Institute, Cambridge, United Kingdom.
Melanie StammersBabraham Institute, Cambridge, United Kingdom.
Laraine CrosslandSignalling Programme, Babraham Institute, Cambridge, United Kingdom.
David OxleyMass Spectrometry Facility, Babraham Institute, Cambridge, United Kingdom.
Hanneke OkkenhaugImaging Facility, Babraham Institute, Cambridge, United Kingdom.
Simon WalkerImaging Facility, Babraham Institute, Cambridge, United Kingdom.
Rachael WalkerFlow Cytometry Facility, Babraham Institute, Cambridge, United Kingdom.
Anne Segonds-PichonBioinformatics Facility, Babraham Institute, Cambridge, United Kingdom.
Yoshinori FukuiDivision of Immunogenetics, Department of Immunobiology and Neuroscience, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
Angeliki MalliriCell Signalling Group, Cancer Research UK Manchester Institute, University of Manchester, Macclesfield, United Kingdom.
Heidi C E WelchSignalling Programme, Babraham Institute, Cambridge, United Kingdom.
Babraham Institute · GBCancer Research UK Manchester Institute · GBKyushu University · JP

Funding

Cancer Research UK 20410
6 · The paper itself

Abstract

Rac GTPases are required for neutrophil adhesion and migration, and for the neutrophil effector responses that kill pathogens. These Rac-dependent functions are impaired when neutrophils lack the activators of Rac, Rac-GEFs from the Prex, Vav, and Dock families. In this study, we demonstrate that Tiam1 is also expressed in neutrophils, governing focal complexes, actin cytoskeletal dynamics, polarisation, and migration, in a manner depending on the integrin ligand to which the cells adhere. Tiam1 is dispensable for the generation of reactive oxygen species but mediates degranulation and NETs release in adherent neutrophils, as well as the killing of bacteria.

Indexed as

IntegrinsNeutrophils14-3-3 ProteinsCD18 AntigensHumansrac GTP-Binding Proteins14-3-3 ProteinsCD18 AntigensIntegrinsrac GTP-Binding ProteinsDock2neutrophilsPrex1RacRac-GEFsmall GTPaseTiam1Vav

Identifiers

PMID38077328
PMCPMC10703174
OpenAlexW4388940436

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.