Evidence map›Paper›PMID 19136961›Full record

ArticleNature immunology2009

Regulation of conformer-specific activation of the integrin LFA-1 by a chemokine-triggered Rho signaling module.

Matteo Bolomini-Vittori, Alessio Montresor, Cinzia Giagulli, Donald Staunton, Barbara Rossi, Marianna Martinello, Gabriela Constantin, Carlo Laudanna

Abstract read
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In one paragraph

Article in Nature immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

77 citing papers in PubMed, 135 citations in OpenAlex.

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  13. β2 integrin activation and signal transduction in leukocyte recruitment.American journal of physiology. Cell physiology · 2021
    Review
  14. PI3K in T Cell Adhesion and Trafficking.Frontiers in immunology · 2021
    Review
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  20. Article

17 more citing papers are in PubMed but not listed here.

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

8 authors at 1 institution in 1 country.

Matteo Bolomini-VittoriUniversity of Verona, School of Medicine, Department of Pathology, Division of General Pathology, Verona 37134, Italy.
Alessio Montresor
Cinzia Giagulli
Donald Staunton
Barbara Rossi
Marianna Martinello
Gabriela Constantin
Carlo Laudanna
University of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulation of the affinity of the beta(2) integrin LFA-1 by chemokines is critical to lymphocyte trafficking, but the signaling mechanisms that control this process are not well understood. Here we investigated the signaling events controlling LFA-1 affinity triggering by chemokines in human primary T lymphocytes. We found that the small GTPase Rac1 mediated chemokine-induced LFA-1 affinity triggering and lymphocyte arrest in high endothelial venules. Unexpectedly, another Rho family member, Cdc42, negatively regulated LFA-1 activation. The Rho effectors PLD1 and PIP5KC were also critical to LFA-1 affinity modulation. Notably, PIP5KC was found to specifically control the transition of LFA-1 from an extended low-intermediate state to a high-affinity state, which correlated with lymphocyte arrest. Thus, chemokines control lymphocyte trafficking by triggering a Rho-dependent signaling cascade leading to conformer-specific modulation of LFA-1 affinity.

Indexed as

AnimalsCell AdhesionChemokinesChemotaxis, LeukocyteEnzyme ActivationHumansLymphocyte Function-Associated Antigen-1Micerho-Associated KinasesRNA, Small InterferingSignal TransductionT-LymphocytesChemokinesLymphocyte Function-Associated Antigen-1rho-Associated KinasesRNA, Small Interfering

Identifiers

PMID19136961
OpenAlexW2038800531

What OpenQuestion 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 OpenQuestion graph.