Evidence map›Paper›PMID 18976916›Full record

ArticleCurrent biology : CB2008

PAR-1 kinase regulates epithelial detachment and directional protrusion of migrating border cells.

Jocelyn A McDonald, Anna Khodyakova, George Aranjuez, Colleen Dudley, Denise J Montell

Abstract read
In one paragraph

Article in Current biology : CB, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.5field-weighted citation impact, top 21% 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

33 citing papers in PubMed, 66 citations in OpenAlex.

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  15. Insulin signaling modulates border cell movement inDevelopment (Cambridge, England) · 2018
    Article
  16. Dendritic space-filling requires a neuronal type-specific extracellular permissive signal inProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  17. Article
  18. Regulation of Cell Polarity by PAR-1/MARK Kinase.Current topics in developmental biology · 2017
    Review
  19. Article
  20. 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 at 2 institutions in 1 country.

Jocelyn A McDonaldDepartment of Molecular Genetics, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA. mcdonaj@ccf.org
Anna Khodyakova
George Aranjuez
Colleen Dudley
Denise J Montell
Cleveland Clinic Lerner College of Medicine · USJohns Hopkins University · US

Funding

Spatiotemporal regulation of collective cell behaviors in Drosophila: Diversity Supplement for Predoctoral TrainingR01GM046425 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI MONTELL, DENISE J. · 1996 to 2025
$11.7M
Making and breaking cell-cell contacts in developmentR01GM073164 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI MONTELL, DENISE J. · 2005 to 2025
$6.2M
Regulation of in vivo cell migration by the polarity protein Par-1R01GM078526 · NIGMS · CLEVELAND CLINIC LERNER COM-CWRU · PI MCDONALD, JOCELYN A · 2008 to 2012
$1.6M
NIGMS NIH HHS R01 GM046425NIGMS NIH HHS R01 GM073164NIGMS NIH HHS R01GM073164NIGMS NIH HHS R01 GM078526NIGMS NIH HHS R01GM078526NIGMS NIH HHS R01GM46425
6 · The paper itself

Abstract

backgroundMany cells that migrate during normal embryonic development or in metastatic cancer first detach from an epithelium. However, this step is often difficult to observe directly in vivo, and the mechanisms controlling the ability of cells to leave the epithelium are poorly understood. In addition, once cells detach, they must assume a migratory phenotype, involving changes in cytoskeletal and signaling dynamics. Drosophila border cells provide a model system in which a combination of forward genetics and live-cell imaging can allow researchers to investigate the cellular and molecular mechanisms of epithelial cell detachment and migration in vivo.

resultsWe identified the Drosophila homolog of the serine/threonine kinase PAR-1 (MARK/Kin1) in a screen for mutations that disrupt border cell migration. Previous studies identified two proteins, Apontic and Notch, that indirectly affect border cell detachment by regulating transcription of downstream targets. In contrast, PAR-1 directly modulates apical-basal polarity between border cells and epithelial cells to promote detachment. Furthermore, PAR-1, but not the apical polarity complex protein PAR-3, promotes the directionality of transient cell protrusions, which border cells require for sensing the chemoattractant gradient.

conclusionsWe conclude that PAR-1-dependent apical-basal polarity is required for proper detachment of migratory border cells from neighboring epithelial cells. Moreover, polarity controlled by PAR-1 influences the ability of migratory cells to sense direction, a critical feature of migration. Thus, this work reveals new insights into two distinct, but essential, steps of epithelial cell migration.

Indexed as

Cell MovementCell PolarityAMP-Activated Protein Kinase KinasesAnimalsCell AdhesionCell Surface ExtensionsDrosophilaDrosophila ProteinsEpithelial CellsGlycogen Synthase Kinase 3Protein KinasesProtein Serine-Threonine KinasesAMP-Activated Protein Kinase KinasesDrosophila ProteinsGlycogen Synthase Kinase 3LKB1 protein, DrosophilaPar-1 protein, DrosophilaProtein KinasesProtein Serine-Threonine Kinases

Identifiers

PMID18976916
PMCPMC2593744
OpenAlexW1984562849

What OpenQuestion holds

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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.