Evidence map›Paper›PMID 26188246›Full record

ArticleDevelopmental biology2015

Cadherin-11 coordinates cellular migration and extracellular matrix remodeling during aortic valve maturation.

Caitlin J Bowen, Jingjing Zhou, Derek C Sung, Jonathan T Butcher

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

31 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Towards Personalized Therapy of Aortic Stenosis.Journal of personalized medicine · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. Observational
  15. Article
  16. Article
  17. Review
  18. The Endocardium and Heart Valves.Cold Spring Harbor perspectives in biology · 2020
    Review
  19. Review
  20. Dynamic Expression Profiles of β-Catenin during Murine Cardiac Valve Development.Journal of cardiovascular development and disease · 2020
    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 1 institution in 1 country.

Caitlin J BowenDepartment of Biomedical Engineering, Cornell University, United States.
Jingjing ZhouDepartment of Biomedical Engineering, Cornell University, United States.
Derek C SungDepartment of Biomedical Engineering, Cornell University, United States.
Jonathan T ButcherDepartment of Biomedical Engineering, Cornell University, United States. Electronic address: jtb47@cornell.edu.
Cornell University · US

Funding

DYNAMIC STUDIES OF COAGULATION AND THROMBOSISR01HL018672 · NHLBI · RICE UNIVERSITY · PI MC INTIRE, LARRY V. · 1985 to 2011
$3.5M
Biomechanical regulation of valvulogenesisR01HL110328 · NHLBI · CORNELL UNIVERSITY · PI BUTCHER, JONATHAN TALBOT · 2011 to 2015
$1.9M
Adhesive signaling in aortic valve development and diseaseR01HL128745 · NHLBI · CORNELL UNIVERSITY · PI BUTCHER, JONATHAN TALBOT · 2015 to 2018
$1.5M
Effects of hydroxyapatite mineralization and valve cell phenotypeR21HL118672 · NHLBI · CORNELL UNIVERSITY · PI BUTCHER, JONATHAN TALBOT · 2013 to 2014
$405k
DYNAMIC STUDIES OF COAGULATION AND THROMBOSISR37HL018672 · NHLBI · RICE UNIVERSITY · PI MC INTIRE, LARRY V. · 1990 to 1999
–
NHLBI NIH HHS HL110328NHLBI NIH HHS HL18672NHLBI NIH HHS R01 HL018672NHLBI NIH HHS R01 HL110328NHLBI NIH HHS R01 HL128745NHLBI NIH HHS R21 HL118672NHLBI NIH HHS R37 HL018672
6 · The paper itself

Abstract

Proper remodeling of the endocardial cushions into thin fibrous valves is essential for gestational progression and long-term function. This process involves dynamic interactions between resident cells and their local environment, much of which is not understood. In this study, we show that deficiency of the cell-cell adhesion protein cadherin-11 (Cad-11) results in significant embryonic and perinatal lethality primarily due to valve related cardiac dysfunction. While endocardial to mesenchymal transformation is not abrogated, mesenchymal cells do not homogeneously cellularize the cushions. These cushions remain thickened with disorganized ECM, resulting in pronounced aortic valve insufficiency. Mice that survive to adulthood maintain thickened and stenotic semilunar valves, but interestingly do not develop calcification. Cad-11 (-/-) aortic valve leaflets contained reduced Sox9 activity, β1 integrin expression, and RhoA-GTP activity, suggesting that remodeling defects are due to improper migration and/or cellular contraction. Cad-11 deletion or siRNA knockdown reduced migration, eliminated collective migration, and impaired 3D matrix compaction by aortic valve interstitial cells (VIC). Cad-11 depleted cells in culture contained few filopodia, stress fibers, or contact inhibited locomotion. Transfection of Cad-11 depleted cells with constitutively active RhoA restored cell phenotypes. Together, these results identify cadherin-11 mediated adhesive signaling for proper remodeling of the embryonic semilunar valves.

Indexed as

Cell MovementAnimalsAortic ValveCadherinsCell PolarityChickensEndocardial CushionsExtracellular MatrixMiceMice, Inbred C57BLMorphogenesisrhoA GTP-Binding ProteinSwineCadherinsosteoblast cadherinrhoA GTP-Binding ProteinAortic valve insufficiencyCalcificationCompactionCongenital heart defectFilopodiaHyperplasiaRhoAStress fiber

Identifiers

PMID26188246
PMCPMC4841269
OpenAlexW918168934

What OpenQuestion holds

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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.