Evidence map›Paper›PMID 21131473›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2011

ZO-1 determines adherens and gap junction localization at intercalated disks.

Joseph A Palatinus, Michael P O'Quinn, Ralph J Barker, Brett S Harris, Jane Jourdan, Robert G Gourdie

Abstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2011. 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. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Understanding the molecular basis of cardiomyopathy.American journal of physiology. Heart and circulatory physiology · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  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

6 authors.

Joseph A PalatinusDepartment of Regenerative Medicine and Cell Biology, Cardiovascular Biology Center, Medical University of South Carolina, 173 Ashley Ave., Charleston, SC, 29425, USA.
Michael P O'Quinn
Ralph J Barker
Brett S Harris
Jane Jourdan
Robert G Gourdie

Funding

REGULATION AND FUNCTION OF THE OUTFLOW SEPTATION COMPLEXP01HL036059 · NHLBI · MEDICAL COLLEGE OF GEORGIA (MCG) · PI KIRBY, MARGARET LOEWY · 1986 to 2004
$8.1M
Patterning by Invasive Mesenchyme in the Embryonic HeartP01HD039946 · NICHD · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI GOURDIE, ROBERT G · 2001 to 2005
$5.9M
PATTERNING OF GAP JUNCTION COUPLING IN DEVELOPING HEARTR01HL056728 · NHLBI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI GOURDIE, ROBERT G · 1997 to 2021
$5.6M
Connexin 43 gap junction dynamics in the diabetic heartF30HL095320 · NHLBI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI PALATINUS, JOSEPH A. · 2009 to 2013
$167k
NHLBI NIH HHS F30 HL095320NHLBI NIH HHS F30-HL-095320NHLBI NIH HHS HL-36059NHLBI NIH HHS HL-56728NICHD NIH HHS HD-39946
6 · The paper itself

Abstract

The disruption of the spatial order of electromechanical junctions at myocyte-intercalated disks (ICDs) is a poorly understood characteristic of many cardiac disease states. Here, in vitro and in vivo evidence is provided that zonula occludens-1 (ZO-1) regulates the organization of gap junctions (GJs) and adherens junctions (AJs) at ICDs. We investigated the contribution of ZO-1 to cell-cell junction localization by expressing a dominant-negative ZO-1 construct (DN-ZO-1) in rat ventricular myocytes (VMs). The expression of DN-ZO-1 in cultured neonatal VMs for 72 h reduced the interaction of ZO-1 and N-cadherin, as assayed by colocalization and coimmunoprecipitation, prompting cytoplasmic internalization of AJ and GJ proteins. DN-ZO-1 expression in adult VMs in vivo also reduced N-cadherin colocalization with ZO-1, a phenomenon not observed when the connexin-43 (Cx43)-ZO-1 interaction was disrupted using a mimetic of the ZO-1-binding ligand from Cx43. DN-ZO-1-infected VMs demonstrated large GJs at the ICD periphery and showed a loss of focal ZO-1 concentrations along plaque edges facing the disk interior. Additionally, there was breakdown of the characteristic ICD pattern of small interior and large peripheral GJs. Continuous DN-ZO-1 expression in VMs over postnatal development reduced ICD-associated Cx43 GJs and increased lateralized and cytoplasmic Cx43. We conclude that ZO-1 regulation of GJ localization is via an association with the N-cadherin multiprotein complex and that this is a key determinant of stable localization of both AJs and GJs at the ICD.

Indexed as

Adaptor Proteins, Signal TransducingAdherens JunctionsAnimalsAnimals, NewbornCadherinsCells, CulturedCell SeparationConnexin 43CytoplasmDependovirusFemaleGap JunctionsGenetic VectorsHeart VentriclesImage Processing, Computer-AssistedImmunoprecipitationAdaptor Proteins, Signal TransducingCadherinsConnexin 43Membrane ProteinsPDZD2 protein, ratPhosphoproteinsTjp1 protein, ratZonula Occludens-1 Protein

Identifiers

PMID21131473
PMCPMC3044061

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.