Evidence map›Paper›PMID 26828861›Full record

ArticlePloS one2016

Cx43-Dependent Skeletal Phenotypes Are Mediated by Interactions between the Hapln1a-ECM and Sema3d during Fin Regeneration.

Jayalakshmi Govindan, Kyaw Min Tun, M Kathryn Iovine

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Pectoral Fin Anomalies inJournal of developmental biology · 2019
    Article
  7. Article
  8. Connexin Communication Compartments and Wound Repair in Epithelial Tissue.International journal of molecular sciences · 2018
    Review
  9. Article
  10. Article
  11. 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

3 authors at 1 institution in 1 country.

Jayalakshmi GovindanDepartment of Biological Sciences, 111 Research Drive, Iacocca B217, Lehigh University, Bethlehem, Pennsylvania, United States of America.
Kyaw Min TunDepartment of Biological Sciences, 111 Research Drive, Iacocca B217, Lehigh University, Bethlehem, Pennsylvania, United States of America.
M Kathryn IovineDepartment of Biological Sciences, 111 Research Drive, Iacocca B217, Lehigh University, Bethlehem, Pennsylvania, United States of America.
Lehigh University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Skeletal development is a tightly regulated process and requires proper communication between the cells for efficient exchange of information. Analysis of fin length mutants has revealed that the gap junction protein Connexin43 (Cx43) coordinates cell proliferation (growth) and joint formation (patterning) during zebrafish caudal fin regeneration. Previous studies have shown that the extra cellular matrix (ECM) protein Hyaluronan and Proteoglycan Link Protein1a (Hapln1a) is molecularly and functionally downstream of Cx43, and that hapln1a knockdown leads to reduction of the glycosaminoglycan hyaluronan. Here we find that the proteoglycan aggrecan is similarly reduced following Hapln1a knockdown. Notably, we demonstrate that both hyaluronan and aggrecan are required for growth and patterning. Moreover, we provide evidence that the Hapln1a-ECM stabilizes the secreted growth factor Semaphorin3d (Sema3d), which has been independently shown to mediate Cx43 dependent phenotypes during regeneration. Double knockdown of hapln1a and sema3d reveal synergistic interactions. Further, hapln1a knockdown phenotypes were rescued by Sema3d overexpression. Therefore, Hapln1a maintains the composition of specific components of the ECM, which appears to be required for the stabilization of at least one growth factor, Sema3d. We propose that the Hapln1a dependent ECM provides the required conditions for Sema3d stabilization and function. Interactions between the ECM and signaling molecules are complex and our study demonstrates the requirement for components of the Hapln1a-ECM for Sema3d signal transduction.

Indexed as

RegenerationAnimal FinsAnimalsBone and BonesConnexin 43Extracellular MatrixExtracellular Matrix ProteinsGene Expression Regulation, DevelopmentalGene Knockdown TechniquesHyaluronic AcidIn Situ HybridizationModels, BiologicalMorpholinosNerve Growth FactorsPhenotypeProtein BindingConnexin 43Extracellular Matrix ProteinsHapln1a protein, zebrafishHyaluronic AcidMorpholinosNerve Growth FactorsProteoglycan Link ProteinProteoglycanssema3d protein, zebrafishSemaphorinsZebrafish Proteins

Identifiers

PMID26828861
PMCPMC4734779
OpenAlexW2256089401

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.