Evidence map›Paper›PMID 25633982›Full record

ArticleDisease models & mechanisms2015

Zebrafish as a model for apolipoprotein biology: comprehensive expression analysis and a role for ApoA-IV in regulating food intake.

Jessica P Otis, Erin M Zeituni, James H Thierer, Jennifer L Anderson, Alexandria C Brown, Erica D Boehm, Derek M Cerchione, Alexis M Ceasrine, Inbal Avraham-Davidi, Hanoch Tempelhof and 2 more

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

61 citing papers in PubMed, 136 citations in OpenAlex.

  1. Article
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  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Zebrafish ApoB-Containing Lipoprotein Metabolism: A Closer Look.Arteriosclerosis, thrombosis, and vascular biology · 2024
    Review
  15. Article
  16. Article
  17. ZebrafishFrontiers in cell and developmental biology · 2024
    Article
  18. Article
  19. Article
  20. From worms to humans: Understanding intestinal lipid metabolism via model organisms.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2023
    Review

1 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

12 authors at 4 institutions in 2 countries.

Jessica P OtisCarnegie Institution for Science, Department of Embryology, Baltimore, MD 21218, USA.
Erin M ZeituniCarnegie Institution for Science, Department of Embryology, Baltimore, MD 21218, USA.
James H ThiererCarnegie Institution for Science, Department of Embryology, Baltimore, MD 21218, USA Johns Hopkins University, Department of Biology, Baltimore, MD 21218, USA.
Jennifer L AndersonCarnegie Institution for Science, Department of Embryology, Baltimore, MD 21218, USA.
Alexandria C BrownCarnegie Institution for Science, Department of Embryology, Baltimore, MD 21218, USA.
Erica D BoehmCarnegie Institution for Science, Department of Embryology, Baltimore, MD 21218, USA Johns Hopkins University, Department of Biology, Baltimore, MD 21218, USA.
Derek M CerchioneCarnegie Institution for Science, Department of Embryology, Baltimore, MD 21218, USA Johns Hopkins University, Department of Biology, Baltimore, MD 21218, USA.
Alexis M CeasrineCarnegie Institution for Science, Department of Embryology, Baltimore, MD 21218, USA Johns Hopkins University, Department of Biology, Baltimore, MD 21218, USA.
Inbal Avraham-DavidiWeizmann Institute of Science, Department of Biological Regulation, Rehovot 7610001, Israel.
Hanoch TempelhofWeizmann Institute of Science, Department of Biological Regulation, Rehovot 7610001, Israel.
Karina YanivWeizmann Institute of Science, Department of Biological Regulation, Rehovot 7610001, Israel.
Steven A FarberCarnegie Institution for Science, Department of Embryology, Baltimore, MD 21218, USA Johns Hopkins University, Department of Biology, Baltimore, MD 21218, USA farber@ciwemb.edu.
Department of Embryology · USCarnegie Institution for Science · USWeizmann Institute of Science · ILJohns Hopkins University · US

Funding

Systematic Vertebrate Functional GenomicsR01GM063904 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI EKKER, STEPHEN CARL · 2001 to 2025
$10.7M
Identifying genes required for digestive physiology and lipid metabolismR01DK093399 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI STEVEN A FARBER, John F Rawls · 2013 to 2026
$7.6M
Cellular and Molecular BiologyT32GM141804 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI John Kim · 2021 to 2026
$5.1M
The role of caveolin 1 in intestinal lipid processing and transportF32DK096786 · NIDDK · CARNEGIE INSTITUTION OF WASHINGTON, D.C. · PI OTIS, JESSICA · 2012 to 2014
$156k
European Research Council 335605NIDDK NIH HHS F32 DK096786NIDDK NIH HHS F32DK096786NIDDK NIH HHS R01 DK093399NIDDK NIH HHS R01DK093399NIGMS NIH HHS R01 GM063904NIGMS NIH HHS R01GM63904NIGMS NIH HHS T32 GM141804
6 · The paper itself

Abstract

Improved understanding of lipoproteins, particles that transport lipids throughout the circulation, is vital to developing new treatments for the dyslipidemias associated with metabolic syndrome. Apolipoproteins are a key component of lipoproteins. Apolipoproteins are proteins that structure lipoproteins and regulate lipid metabolism through control of cellular lipid exchange. Constraints of cell culture and mouse models mean that there is a need for a complementary model that can replicate the complex in vivo milieu that regulates apolipoprotein and lipoprotein biology. Here, we further establish the utility of the genetically tractable and optically clear larval zebrafish as a model of apolipoprotein biology. Gene ancestry analyses were implemented to determine the closest human orthologs of the zebrafish apolipoprotein A-I (apoA-I), apoB, apoE and apoA-IV genes and therefore ensure that they have been correctly named. Their expression patterns throughout development were also analyzed, by whole-mount mRNA in situ hybridization (ISH). The ISH results emphasized the importance of apolipoproteins in transporting yolk and dietary lipids: mRNA expression of all apolipoproteins was observed in the yolk syncytial layer, and intestinal and liver expression was observed from 4-6 days post-fertilization (dpf). Furthermore, real-time PCR confirmed that transcription of three of the four zebrafish apoA-IV genes was increased 4 hours after the onset of a 1-hour high-fat feed. Therefore, we tested the hypothesis that zebrafish ApoA-IV performs a conserved role to that in rat in the regulation of food intake by transiently overexpressing ApoA-IVb.1 in transgenic larvae and quantifying ingestion of co-fed fluorescently labeled fatty acid during a high-fat meal as an indicator of food intake. Indeed, ApoA-IVb.1 overexpression decreased food intake by approximately one-third. This study comprehensively describes the expression and function of eleven zebrafish apolipoproteins and serves as a springboard for future investigations to elucidate their roles in development and disease in the larval zebrafish model.

Indexed as

AnimalsApolipoproteins AApolipoproteins BApolipoproteins EDiet, High-FatEatingGene Expression Regulation, DevelopmentalIntestinal MucosaModels, AnimalPhylogenyRNA, MessengerTranscription, GeneticZebrafishZebrafish ProteinsApoa4b protein, zebrafishapolipoprotein A-IVApolipoproteins AApolipoproteins BApolipoproteins ERNA, MessengerZebrafish ProteinsApolipoprotein A-IApolipoprotein A-IVApolipoprotein BApolipoprotein EDevelopmental expression patternsmRNA in situ hybridizationRegulation of food intakeZebrafish

Identifiers

PMID25633982
PMCPMC4348566
OpenAlexW2151583983

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.