Evidence map›Paper›PMID 26905427›Full record

ArticleScience signaling2016

Dynamic regulation of neutrophil polarity and migration by the heterotrimeric G protein subunits Gαi-GTP and Gβγ.

Chinmay R Surve, Jesi Y To, Sundeep Malik, Minsoo Kim, Alan V Smrcka

Abstract read
In one paragraph

Article in Science signaling, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
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

23 citing papers in PubMed.

  1. Article
  2. Nurr1 Orchestrates Claustrum Development and Functionality.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. ELMO1 Deficiency Reduces Neutrophil Chemotaxis in Murine Peritonitis.International journal of molecular sciences · 2023
    Article
  7. Article
  8. Article
  9. A network of GαScience signaling · 2022
    Article
  10. Review
  11. GαJournal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  12. Effects of venoms on neutrophil respiratory burst: a major inflammatory function.The journal of venomous animals and toxins including tropical diseases · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Activated heterotrimeric G protein αThe Journal of biological chemistry · 2018
    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

5 authors.

Chinmay R SurveDepartment of Biochemistry and Biophysics, University of Rochester, Rochester, NY 14642, USA.
Jesi Y ToDepartment of Pharmacology and Physiology, University of Rochester, Rochester, NY 14642, USA.
Sundeep MalikDepartment of Pharmacology and Physiology, University of Rochester, Rochester, NY 14642, USA.
Minsoo KimDepartment of Immunology and Microbiology, University of Rochester, Rochester, NY 14642, USA.
Alan V SmrckaDepartment of Biochemistry and Biophysics, University of Rochester, Rochester, NY 14642, USA. Department of Pharmacology and Physiology, University of Rochester, Rochester, NY 14642, USA. alan_smrcka@URMC.rochester.edu.

Funding

Tissue regulation of T cell function - Reagents CoreP01AI102851 · NIAID · UNIVERSITY OF ROCHESTER · PI Deborah J Fowell · 2014 to 2026
$26.0M
Selective Targeting of G Protein beta gamma Subunits with Small MoleculesR01GM081772 · NIGMS · UNIVERSITY OF ROCHESTER · PI SMRCKA, ALAN V. · 2008 to 2017
$3.2M
NIAID NIH HHS P01 AI102851NIAID NIH HHS P01AI102851NIGMS NIH HHS R01 GM081772NIGMS NIH HHS R01GM081772
6 · The paper itself

Abstract

Activation of the Gi family of heterotrimeric guanine nucleotide-binding proteins (G proteins) releases βγ subunits, which are the major transducers of chemotactic G protein-coupled receptor (GPCR)-dependent cell migration. The small molecule 12155 binds directly to Gβγ and activates Gβγ signaling without activating the Gαi subunit in the Gi heterotrimer. We used 12155 to examine the relative roles of Gαi and Gβγ activation in the migration of neutrophils on surfaces coated with the integrin ligand intercellular adhesion molecule-1 (ICAM-1). We found that 12155 suppressed basal migration by inhibiting the polarization of neutrophils and increasing their adhesion to ICAM-1-coated surfaces. GPCR-independent activation of endogenous Gαi and Gβγ with the mastoparan analog Mas7 resulted in normal migration. Furthermore, 12155-treated cells expressing a constitutively active form of Gαi1 became polarized and migrated. The extent and duration of signaling by the second messenger cyclic adenosine monophosphate (cAMP) were enhanced by 12155. Inhibiting the activity of cAMP-dependent protein kinase (PKA) restored the polarity of 12155-treated cells but did not decrease their adhesion to ICAM-1 and failed to restore migration. Together, these data provide evidence for a direct role of activated Gαi in promoting cell polarization through a cAMP-dependent mechanism and in inhibiting adhesion through a cAMP-independent mechanism.

Indexed as

AnimalsCell MovementGTP-Binding Protein alpha Subunits, Gi-GoGTP-Binding Protein beta SubunitsHL-60 CellsHumansIntercellular Adhesion Molecule-1Intercellular Signaling Peptides and ProteinsMicePeptidesGTP-Binding Protein alpha Subunits, Gi-GoGTP-Binding Protein beta SubunitsICAM1 protein, humanIcam1 protein, mouseIntercellular Adhesion Molecule-1Intercellular Signaling Peptides and ProteinsMas7 protein, syntheticPeptides

Identifiers

PMID26905427
PMCPMC6364554

What OpenQuestion holds

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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.