Evidence map›Paper›PMID 21282462›Full record

ArticleThe Journal of cell biology2011

The serine/threonine kinase Par1b regulates epithelial lumen polarity via IRSp53-mediated cell-ECM signaling.

David Cohen, Dawn Fernandez, Francisco Lázaro-Diéguez, Anne Müsch

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2011. 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
3.3field-weighted citation impact, top 7% 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, 59 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Mechanism of IRSp53 inhibition by 14-3-3.Nature communications · 2019
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Signaling Networks in Epithelial Tube Formation.Cold Spring Harbor perspectives in biology · 2017
    Review
  15. Review
  16. Partitioning-Defective 1a/b Depletion Impairs Glomerular and Proximal Tubule Development.Journal of the American Society of Nephrology : JASN · 2016
    Article
  17. Article
  18. Integrins and epithelial cell polarity.Journal of cell science · 2014
    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

4 authors at 2 institutions in 1 country.

David CohenDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, The Bronx, NY 10461, USA.
Dawn Fernandez
Francisco Lázaro-Diéguez
Anne Müsch
Albert Einstein College of Medicine · USThe Bronx Defenders · US

Funding

Mechanisms of luminal protein targeting in kidney and hepatic epithelial cellsR01DK064842 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI MUESCH, ANNE · 2005 to 2015
$4.1M
NIDDK NIH HHS R01 DK064842
6 · The paper itself

Abstract

The serine/threonine kinase Par1b promotes cell-cell adhesion and determines the polarity of the luminal domain in epithelial cells. In this study, we demonstrate that Par1b also regulates cell-extracellular matrix (ECM) signaling in kidney-derived Madin-Darby canine kidney (MDCK) cells and identified the rho-guanosine triphosphatase adaptor and scaffolding protein IRSp53 as a Par1b substrate involved in this pathway. Par1b overexpression inhibits basal lamina formation, cell spreading, focal adhesion, stress fiber formation, and compaction, whereas Par1b depletion has the opposite effect. IRSp53 depletion mimics Par1b overexpression on cell-ECM signaling and lumen polarity but had no effect on adherens junction formation. Par1b directly phosphorylates IRSp53 on S366 in cell lysates and stimulates phosphorylation on S453/3/5 via an indirect mechanism. A Par1b phosphorylation-deficient IRSp53 mutant but not the wild-type protein efficiently rescues both the cell spreading and the lumen polarity defects in Par1b MDCK cells. Our data suggest a model in which Par1b phosphorylation prevents recruitment of IRSp53 effector proteins to its Src homology domain 3 by promoting 14-3-3 binding in the vicinity of that domain.

Indexed as

Signal Transduction14-3-3 ProteinsAnimalsCell AdhesionCell PolarityCells, CulturedDogsEpithelial CellsExtracellular MatrixNerve Tissue ProteinsProtein Serine-Threonine Kinasessrc Homology Domains14-3-3 ProteinsNerve Tissue ProteinsProtein Serine-Threonine Kinases

Identifiers

PMID21282462
PMCPMC3101094
OpenAlexW2153333049

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.