Evidence map›Paper›PMID 30462573›Full record

ArticleMolecular biology of the cell2019

An endogenous chemorepellent directs cell movement by inhibiting pseudopods at one side of cells.

Ramesh Rijal, Kristen M Consalvo, Christopher K Lindsey, Richard H Gomer

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. The Proteome ofProteomes · 2026
    Article
  2. Article
  3. Article
  4. Two endogenousProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Article
  7. Starvation Induces Extracellular Accumulation of Polyphosphate inInternational journal of molecular sciences · 2023
    Article
  8. Article
  9. Sex-Based Differences in Human Neutrophil Chemorepulsion.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  10. Article
  11. Identification of novel proteins in themicroPublication biology · 2022
    Article
  12. Article
  13. Altered protein secretion in Batten disease.Disease models & mechanisms · 2021
    Review
  14. Article
  15. Review
  16. UsingFrontiers in cell and developmental biology · 2021
    Review
  17. Article
  18. Extracellular signaling in Dictyostelium.The International journal of developmental biology · 2019
    Review
  19. Review
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

4 authors at 1 institution in 1 country.

Ramesh RijalDepartment of Biology, Texas A&M University, College Station, TX 77843-3474.
Kristen M ConsalvoDepartment of Biology, Texas A&M University, College Station, TX 77843-3474.
Christopher K LindseyDepartment of Biology, Texas A&M University, College Station, TX 77843-3474.
Richard H GomerDepartment of Biology, Texas A&M University, College Station, TX 77843-3474.
Texas A&M University · US

Funding

Elucidation of a eukaryotic chemorepulsion mechanismR01GM118355 · NIGMS · TEXAS A&M UNIVERSITY · PI GOMER, RICHARD H · 2016 to 2019
$1.2M
NIGMS NIH HHS R01 GM118355
6 · The paper itself

Abstract

Eukaryotic chemoattraction signal transduction pathways, such as those used by Dictyostelium discoideum to move toward cAMP, use a G protein-coupled receptor to activate multiple conserved pathways such as PI3 kinase/Akt/PKB to induce actin polymerization and pseudopod formation at the front of a cell, and PTEN to localize myosin II to the rear of a cell. Relatively little is known about chemorepulsion. We previously found that AprA is a chemorepellent protein secreted by Dictyostelium cells. Here we used 29 cell lines with disruptions of cAMP and/or AprA signal transduction pathway components, and delineated the AprA chemorepulsion pathway. We find that AprA uses a subset of chemoattraction signal transduction pathways including Ras, protein kinase A, target of rapamycin (TOR), phospholipase A, and ERK1, but does not require the PI3 kinase/Akt/PKB and guanylyl cyclase pathways to induce chemorepulsion. Possibly as a result of not using the PI3 kinase/Akt/PKB pathway and guanylyl cyclases, AprA does not induce actin polymerization or increase the pseudopod formation rate, but rather appears to inhibit pseudopod formation at the side of cells closest to the source of AprA.

Indexed as

ChemotaxisActinsCalcium ChannelsCell PolarityCyclic AMPCytoskeletonDictyosteliumExtracellular Signal-Regulated MAP KinasesGuanylate CyclaseModels, BiologicalMutationMyosin Type IIPhosphatidylinositol 3-KinasesPhospholipasesProtein Kinase CProtein TransportActinsCalcium ChannelsCyclic AMPExtracellular Signal-Regulated MAP KinasesGuanylate CyclaseMyosin Type IIPhosphatidylinositol 3-KinasesPhospholipasesProtein Kinase CProtozoan Proteinsras ProteinsReceptors, G-Protein-Coupled

Identifiers

PMID30462573
PMCPMC6589559
OpenAlexW2901611003

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.