Evidence map›Paper›PMID 29441573›Full record

ArticleJournal of anatomy2018

Widening control of fin inter-rays in zebrafish and inferences about actinopterygian fins.

Carmen Murciano, Salvador Cazorla-Vázquez, Javier Gutiérrez, Juan Antonio Hijano, Josefa Ruiz-Sánchez, Laura Mesa-Almagro, Flores Martín-Reyes, Tahía Diana Fernández, Manuel Marí-Beffa

Open access · greenAbstract read
In one paragraph

Article in Journal of anatomy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 3 institutions in 1 country.

Carmen MurcianoDepartment of Cell Biology, Genetics and Physiology, Biomedical Research Institute of Málaga (IBIMA), Faculty of Science, University of Málaga, Málaga, Spain.
Salvador Cazorla-VázquezDepartment of Cell Biology, Genetics and Physiology, Biomedical Research Institute of Málaga (IBIMA), Faculty of Science, University of Málaga, Málaga, Spain.
Javier GutiérrezDepartment of Cell Biology, Genetics and Physiology, Biomedical Research Institute of Málaga (IBIMA), Faculty of Science, University of Málaga, Málaga, Spain.
Juan Antonio HijanoDepartment of Cell Biology, Genetics and Physiology, Biomedical Research Institute of Málaga (IBIMA), Faculty of Science, University of Málaga, Málaga, Spain.
Josefa Ruiz-SánchezDepartment of Cell Biology, Genetics and Physiology, Biomedical Research Institute of Málaga (IBIMA), Faculty of Science, University of Málaga, Málaga, Spain.
Laura Mesa-AlmagroDepartment of Cell Biology, Genetics and Physiology, Biomedical Research Institute of Málaga (IBIMA), Faculty of Science, University of Málaga, Málaga, Spain.
Flores Martín-ReyesDepartment of Cell Biology, Genetics and Physiology, Biomedical Research Institute of Málaga (IBIMA), Faculty of Science, University of Málaga, Málaga, Spain.
Tahía Diana FernándezResearch Laboratory, IBIMA-Regional University Hospital of Málaga, Málaga, Spain.
Manuel Marí-BeffaDepartment of Cell Biology, Genetics and Physiology, Biomedical Research Institute of Málaga (IBIMA), Faculty of Science, University of Málaga, Málaga, Spain.ORCID 0000-0001-7033-5701
Instituto de Investigación Biomédica de Málaga · ESBiomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine · ESHospital Regional Universitario de Málaga · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The amputation of a teleost fin rapidly triggers an intricate maze of hierarchically regulated signalling processes which ultimately reconstruct the diverse tissues of the appendage. Whereas the generation of the fin pattern along the proximodistal axis brings with it several well-known developmental regulators, the mechanisms by which the fin widens along its dorsoventral axis remain poorly understood. Utilizing the zebrafish as an experimental model of fin regeneration and studying more than 1000 actinopterygian species, we hypothesized a connection between specific inter-ray regulatory mechanisms and the morphological variability of inter-ray membranes found in nature. To tackle these issues, both cellular and molecular approaches have been adopted and our results suggest the existence of two distinguishable inter-ray areas in the zebrafish caudal fin, a marginal and a central region. The present work associates the activity of the cell membrane potassium channel kcnk5b, the fibroblast growth factor receptor 1 and the sonic hedgehog pathway to the control of several cell functions involved in inter-ray wound healing or dorsoventral regeneration of the zebrafish caudal fin. This ray-dependent regulation controls cell migration, cell-type patterning and gene expression. The possibility that modifications of these mechanisms are responsible for phenotypic variations found in euteleostean species, is discussed.

Indexed as

RegenerationAnimal FinsAnimalsAnimals, Genetically ModifiedCell MovementFemaleGene ExpressionHedgehog ProteinsMalePotassium Channels, Tandem Pore DomainReceptor, Fibroblast Growth Factor, Type 1ZebrafishZebrafish ProteinsHedgehog ProteinsPotassium Channels, Tandem Pore DomainReceptor, Fibroblast Growth Factor, Type 1Shha protein, zebrafishZebrafish Proteinsactinopterygiieuteleosteievo-devofibroblast growth factor receptor 1fin regenerationinter-rayknck5b

Identifiers

PMID29441573
PMCPMC6480674
OpenAlexW2791248489

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.