Evidence map›Paper›PMID 11449002›Full record

ArticleThe Journal of cell biology2001

Modulation of mouse neural crest cell motility by N-cadherin and connexin 43 gap junctions.

X Xu, W E Li, G Y Huang, R Meyer, T Chen, Y Luo, M P Thomas, G L Radice, C W Lo

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

75 citing papers in PubMed, 224 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. The Role of GJD2(Cx36) in Refractive Error Development.Investigative ophthalmology & visual science · 2022
    Review
  10. Article
  11. Cell Adhesion Molecules in Plasticity and Metastasis.Molecular cancer research : MCR · 2021
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Gap Junction Coding Innexin inFrontiers in synaptic neuroscience · 2020
    Article
  17. Review
  18. Article
  19. Review
  20. An emerging tumor invasion mechanism about the collective cell migration.American journal of translational research · 2019
    Review

15 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

9 authors at 1 institution in 1 country.

X XuBiology Department, Goddard Laboratory, University of Pennsylvania, Philadelphia, PA 19104, USA.
W E Li
G Y Huang
R Meyer
T Chen
Y Luo
M P Thomas
G L Radice
C W Lo
University of Pennsylvania · US

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
TRANSGENIC MODULATION OF GAP JUNCTION INTERACTIONSR01HD036457 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI SCHULTZ, RICHARD M · 1998 to 2001
$614k
CELL ADHESION AND REGULATION OF CARDIAC MYOCYTE FUNCTIONR01HL057554 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI RADICE, GLENN LAWRENCE · 1997 to 2001
$520k
NHLBI NIH HHS HL36059NHLBI NIH HHS HL57554NHLBI NIH HHS P01 HL036059NICHD NIH HHS HD36457NICHD NIH HHS HD39946NICHD NIH HHS P01 HD039946
6 · The paper itself

Abstract

Connexin 43 (Cx43alpha1) gap junction has been shown to have an essential role in mediating functional coupling of neural crest cells and in modulating neural crest cell migration. Here, we showed that N-cadherin and wnt1 are required for efficient dye coupling but not for the expression of Cx43alpha1 gap junctions in neural crest cells. Cell motility was found to be altered in the N-cadherin-deficient neural crest cells, but the alterations were different from that elicited by Cx43alpha1 deficiency. In contrast, wnt1-deficient neural crest cells showed no discernible change in cell motility. These observations suggest that dye coupling may not be a good measure of gap junction communication relevant to motility. Alternatively, Cx43alpha1 may serve a novel function in motility. We observed that p120 catenin (p120ctn), an Armadillo protein known to modulate cell motility, is colocalized not only with N-cadherin but also with Cx43alpha1. Moreover, the subcellular distribution of p120ctn was altered with N-cadherin or Cx43alpha1 deficiency. Based on these findings, we propose a model in which Cx43alpha1 and N-cadherin may modulate neural crest cell motility by engaging in a dynamic cross-talk with the cell's locomotory apparatus through p120ctn signaling.

Indexed as

Gap JunctionsZebrafish ProteinsAnimalsBromodeoxyuridineCadherinsCateninsCell Adhesion MoleculesCell CommunicationCell DivisionCell MovementCells, CulturedConnexin 43Delta CateninGenotypeImmunohistochemistryMiceBromodeoxyuridineCadherinsCateninsCell Adhesion MoleculesConnexin 43Ctnnd1 protein, mouseDelta CateninPhosphoproteinsProto-Oncogene ProteinsWnt1 ProteinWnt1 protein, mouseWnt ProteinsZebrafish Proteins

Identifiers

PMID11449002
PMCPMC2196865
OpenAlexW2110049914

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.