Evidence map›Paper›PMID 28864771›Full record

ArticleThe Journal of biological chemistry2017

Two independent but synchronized Gβγ subunit-controlled pathways are essential for trailing-edge retraction during macrophage migration.

Praneeth Siripurapu, Dinesh Kankanamge, Kasun Ratnayake, Kanishka Senarath, Ajith Karunarathne

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. PLCβs are recruited to the plasma membrane in macrophages by both Gβγ and GαProceedings of the National Academy of Sciences of the United States of America · 2026
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  15. Statins Perturb GMolecular pharmacology · 2019
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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 at 1 institution in 1 country.

Praneeth SiripurapuFrom the Department of Chemistry and Biochemistry, University of Toledo, Toledo, Ohio 43606.
Dinesh KankanamgeFrom the Department of Chemistry and Biochemistry, University of Toledo, Toledo, Ohio 43606.
Kasun RatnayakeFrom the Department of Chemistry and Biochemistry, University of Toledo, Toledo, Ohio 43606.
Kanishka SenarathFrom the Department of Chemistry and Biochemistry, University of Toledo, Toledo, Ohio 43606.
Ajith KarunarathneFrom the Department of Chemistry and Biochemistry, University of Toledo, Toledo, Ohio 43606 Ajith.karunarathne@utoledo.edu.
University of Toledo · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemokine-induced directional cell migration is a universal cellular mechanism and plays crucial roles in numerous biological processes, including embryonic development, immune system function, and tissue remodeling and regeneration. During the migration of a stationary cell, the cell polarizes, forms lamellipodia at the leading edge (LE), and triggers the concurrent retraction of the trailing edge (TE). During cell migration governed by inhibitory G protein (G

Indexed as

Cell MovementActomyosinAnimalsCalciumGTP-Binding Protein beta SubunitsGTP-Binding Protein gamma SubunitsHeLa CellsHumansMacrophagesMicePhospholipase C betaRAW 264.7 CellsrhoA GTP-Binding Proteinrho GTP-Binding ProteinsActomyosinCalciumGTP-Binding Protein beta SubunitsGTP-Binding Protein gamma SubunitsPhospholipase C betarhoA GTP-Binding ProteinRHOA protein, humanRhoA protein, mouserho GTP-Binding Proteinscalciumcell migrationG proteinG protein-coupled receptor (GPCR)opsinoptogeneticsRetinalsignal transduction

Identifiers

PMID28864771
PMCPMC5655523
OpenAlexW2753665850

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.