Evidence map›Paper›PMID 21730140›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Ezrin-mediated apical integrity is required for intestinal homeostasis.

Jessica B Casaletto, Ichiko Saotome, Marcello Curto, Andrea I McClatchey

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

61 citing papers in PubMed, 114 citations in OpenAlex.

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  13. Rotavirus-mediated DGAT1 degradation: A pathophysiological mechanism of viral-induced malabsorptive diarrhea.Proceedings of the National Academy of Sciences of the United States of America · 2023
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1 more citing papers are in PubMed but not listed here.

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.

Jessica B CasalettoMassachusetts General Hospital Center for Cancer Research and Department of Pathology, Harvard Medical School, Charlestown, MA 02129, USA.
Ichiko Saotome
Marcello Curto
Andrea I McClatchey
Center for Cancer Research · USHarvard University · US

Funding

Molecular Function of the Nf2 Tumor Suppressor, MerlinR01CA113733 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI MCCLATCHEY, ANDREA I · 2005 to 2014
$3.1M
Functional analysis of ERM proteins in epithelial morphogenesisR01GM087558 · NIGMS · UNIVERSITY OF CHICAGO · PI FEHON, RICHARD G, MCCLATCHEY, ANDREA I · 2010 to 2013
$1.9M
NCI NIH HHS R01 CA113733NIGMS NIH HHS R01 GM087558NIGMS NIH HHS R01GM087558
6 · The paper itself

Abstract

Individual cell types are defined by architecturally and functionally specialized cortical domains. The Ezrin, Radixin, and Moesin (ERM) proteins play a major role in organizing cortical domains by assembling membrane protein complexes and linking them to the cortical actin cytoskeleton. Many studies have focused on the individual roles of the ERM proteins in stabilizing the membrane-cytoskeleton interface, controlling the distribution and function of apical membrane complexes, regulating the small GTPase Rho, or establishing cell-cell junctions. We previously found that deletion of the mouse Ezrin gene yields severe defects in apical integrity throughout the developing intestinal epithelium, resulting in incomplete villus morphogenesis and neonatal death. However, the molecular function of Ezrin in building the apical surface of the intestinal epithelium was not clear. By deleting Ezrin in the adult mouse intestinal epithelium, we provide evidence that Ezrin performs multiple molecular functions that collaborate to build the functional apical surface of the intestinal epithelium in vivo. The loss of Ezrin-mediated apical integrity in the adult intestine yields severe morphological consequences during intestinal homeostasis, including defects in cell geometry, extrusion, junctional remodeling, and spindle orientation. Surprisingly, deletion of Ezrin either before or after villus morphogenesis yields villus fusion, revealing a previously unrecognized step in intestinal homeostasis. Our studies indicate that the function of Ezrin in building and maintaining the apical domain is essential not only for intestinal morphogenesis but also for homeostasis in the mature intestine.

Indexed as

AnimalsCytoskeletal ProteinsEzrinFluorescent Antibody TechniqueGene DeletionHistological TechniquesHomeostasisImmunoblottingImmunohistochemistryImmunoprecipitationIntestinal MucosaMiceMice, TransgenicMicroscopy, Electron, TransmissionMorphogenesisCytoskeletal ProteinsEzrin

Identifiers

PMID21730140
PMCPMC3141968
OpenAlexW2081155310

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.