Evidence map›Paper›PMID 7536748›Full record

ArticleThe Journal of cell biology1995

Plasticity in epithelial cell phenotype: modulation by expression of different cadherin cell adhesion molecules.

J A Marrs, C Andersson-Fisone, M C Jeong, L Cohen-Gould, C Zurzolo, I R Nabi, E Rodriguez-Boulan, W J Nelson

Abstract read
In one paragraph

Article in The Journal of cell biology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed.

  1. Review
  2. Review
  3. Epigenetic Regulation of EMP/EMT-Dependent Fibrosis.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Overview of the Muscle Cytoskeleton.Comprehensive Physiology · 2017
    Review
  7. The Apical Localization of NaFrontiers in physiology · 2016
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Salt-inducible kinase 1 regulates E-cadherin expression and intercellular junction stability.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2012
    Article
  15. RPE barrier breakdown in diabetic retinopathy: seeing is believing.Journal of ocular biology, diseases, and informatics · 2011
    Article
  16. Article
  17. Review
  18. Sodium pump localization in epithelia.Journal of bioenergetics and biomembranes · 2007
    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

8 authors.

J A MarrsDepartment of Molecular and Cellular Physiology, Stanford University School of Medicine, California 94305-5426, USA.
C Andersson-Fisone
M C Jeong
L Cohen-Gould
C Zurzolo
I R Nabi
E Rodriguez-Boulan
W J Nelson

Funding

RETINA--REVERSED POLARITY IN RPER01EY008538 · NEI · WEILL MEDICAL COLL OF CORNELL UNIV · PI RODRIGUEZ-BOULAN, ENRIQUE J · 1991 to 2020
$13.4M
Topogenesis of NA/K-ATPASE in Polarized Epithelial CellsR37GM035527 · NIGMS · STANFORD UNIVERSITY · PI NELSON, W. JAMES · 2003 to 2012
$7.4M
Topogenesis of Na/K-ATPase in Polarized MDCK Epithelial CellsR01GM035527 · NIGMS · STANFORD UNIVERSITY · PI NELSON, W. JAMES · 1986 to 2015
$3.3M
NEI NIH HHS EY08538-04NIGMS NIH HHS GM 35527
6 · The paper itself

Abstract

A primary function of cadherins is to regulate cell adhesion. Here, we demonstrate a broader function of cadherins in the differentiation of specialized epithelial cell phenotypes. In situ, the rat retinal pigment epithelium (RPE) forms cell-cell contacts within its monolayer, and at the apical membrane with the neural retina; Na+, K(+)-ATPase and the membrane cytoskeleton are restricted to the apical membrane. In vitro, RPE cells (RPE-J cell line) express an endogenous cadherin, form adherens junctions and a tight monolayer, but Na+,K(+)-ATPase is localized to both apical and basal-lateral membranes. Expression of E-cadherin in RPE-J cells results in restriction and accumulation of both Na+,K(+)-ATPase and the membrane cytoskeleton at the lateral membrane; these changes correlate with the synthesis of a different ankyrin isoform. In contrast to both RPE in situ and RPE-J cells that do not form desmosomes, E-cadherin expression in RPE-J cells induces accumulation of desmoglein mRNA, and assembly of desmosome-keratin complexes at cell-cell contacts. These results demonstrate that cadherins directly affect epithelial cell phenotype by remodeling the distributions of constitutively expressed proteins and by induced accumulation of specific proteins, which together lead to the generation of structurally and functionally distinct epithelial cell types.

Indexed as

Amino Acid SequenceAnimalsAnkyrinsCadherinsCell CommunicationCell DifferentiationCell LineCytoskeletal ProteinsDesmogleinsDesmoplakinsDesmosomesIntermediate FilamentsKeratinsMolecular Sequence DataMolecular WeightPhenotypeAnkyrinsCadherinsCytoskeletal ProteinsDesmogleinsDesmoplakinsKeratinsRNA, MessengerSodium-Potassium-Exchanging ATPase

Identifiers

PMID7536748
PMCPMC2199912

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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.