Evidence map›Paper›PMID 29040309›Full record

ArticlePloS one2017

Targeted Pth4-expressing cell ablation impairs skeletal mineralization in zebrafish.

Paula Suarez-Bregua, Ankur Saxena, Marianne E Bronner, Josep Rotllant

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  7. Type II NaPflugers Archiv : European journal of physiology · 2019
    Review
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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 3 institutions in 2 countries.

Paula Suarez-BreguaAquatic Molecular Pathobiology Group, Institute of Marine Research (IIM-CSIC), Vigo, Spain.
Ankur SaxenaDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, United States of America.
Marianne E BronnerDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, United States of America.
Josep RotllantAquatic Molecular Pathobiology Group, Institute of Marine Research (IIM-CSIC), Vigo, Spain.
Instituto de Investigacións Mariñas · ESCalifornia Institute of Technology · USUniversity of Illinois Chicago · US

Funding

Gene Regulatory Network Controlling Premigratory Cranial vs Trunk Neural CrestR01DE024157 · NIDCR · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BRONNER, MARIANNE · 2014 to 2025
$4.0M
NIDCR NIH HHS R01 DE024157
6 · The paper itself

Abstract

Skeletal development and mineralization are essential processes driven by the coordinated action of neural signals, circulating molecules and local factors. Our previous studies revealed that the novel neuropeptide Pth4, synthesized by hypothalamic cells, was involved in bone metabolism via phosphate regulation in adult zebrafish. Here, we investigate the role of pth4 during skeletal development using single-cell resolution, two-photon laser ablation of Pth4:eGFP-expressing cells and confocal imaging in vivo. Using a stable transgenic Pth4:eGFP zebrafish line, we identify Pth4:eGFP-expressing cells as post-mitotic neurons. After targeted ablation of eGFP-expressing cells in the hypothalamus, the experimental larvae exhibited impaired mineralization of the craniofacial bones whereas cartilage development was normal. In addition to a decrease in pth4 transcript levels, we noted altered expression of phex and entpd5, genes associated with phosphate homeostasis and mineralization, as well as a delay in the expression of osteoblast differentiation markers such as sp7 and sparc. Taken together, these results suggest that Pth4-expressing hypothalamic neurons participate in the regulation of bone metabolism, possibly through regulating phosphate balance during zebrafish development.

Indexed as

AnimalsAnimals, Genetically ModifiedBone and BonesBone DensityCalcification, PhysiologicCalcinosisEmbryo, NonmammalianGene Expression Regulation, DevelopmentalGenes, ReporterGreen Fluorescent ProteinsHypothalamusLarvaLaser TherapyNeuronsOsteoblastsOsteogenesisentpd5a protein, zebrafishGreen Fluorescent ProteinsOsteonectinParathyroid Hormone-Related ProteinPHEX Phosphate Regulating Neutral EndopeptidasePhosphatesPth4 protein, zebrafishPyrophosphatasessp7 protein, zebrafishSp7 Transcription FactorTranscription FactorsXenopus ProteinsZebrafish Proteins

Identifiers

PMID29040309
PMCPMC5645135
OpenAlexW2765202066

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.