Evidence map›Paper›PMID 28017862›Full record

ArticleBiochimica et biophysica acta. Molecular and cell biology of lipids2017

Critical role of the peroxisomal protein PEX16 in white adipocyte development and lipid homeostasis.

Dina C Hofer, Ariane R Pessentheiner, Helmut J Pelzmann, Stefanie Schlager, Corina T Madreiter-Sokolowski, Dagmar Kolb, Thomas O Eichmann, Gerald Rechberger, Martin Bilban, Wolfgang F Graier and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Biochimica et biophysica acta. Molecular and cell biology of lipids, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. 1-Marine drugs · 2022
    Article
  4. Article
  5. Review
  6. Article
  7. Knockdown of PEX16 Induces Autophagic Degradation of Peroxisomes.International journal of molecular sciences · 2021
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  14. Review
  15. Pex11a deficiency causes dyslipidaemia and obesity in mice.Journal of cellular and molecular medicine · 2019
    Article
  16. Article
  17. Review
  18. 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

12 authors at 4 institutions in 1 country.

Dina C HoferInstitute of Biochemistry, Graz University of Technology, Austria.
Ariane R PessentheinerInstitute of Biochemistry, Graz University of Technology, Austria.
Helmut J PelzmannInstitute of Biochemistry, Graz University of Technology, Austria.
Stefanie SchlagerInstitute of Molecular Biology and Biochemistry, Medical University of Graz, Austria.
Corina T Madreiter-SokolowskiInstitute of Molecular Biology and Biochemistry, Medical University of Graz, Austria.
Dagmar KolbInstitute of Cell Biology, Histology and Embryology/Center for Medical Research, Medical University of Graz, Austria.
Thomas O EichmannInstitute of Molecular Biosciences, University of Graz, Austria.
Gerald RechbergerInstitute of Molecular Biosciences, University of Graz, Austria; Omics-Center, BioTechMed, Graz, Austria.
Martin BilbanDepartment of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria.
Wolfgang F GraierInstitute of Molecular Biology and Biochemistry, Medical University of Graz, Austria.
Dagmar KratkyInstitute of Molecular Biology and Biochemistry, Medical University of Graz, Austria.
Juliane G Bogner-StraussInstitute of Biochemistry, Graz University of Technology, Austria. Electronic address: juliane.bogner-strauss@tugraz.at.
Medical University of Graz · ATGraz University of Technology · ATUniversity of Graz · ATMedical University of Vienna · AT

Funding

Austrian Science Fund FWF P 24143Austrian Science Fund FWF P 27070Austrian Science Fund FWF P 27108Austrian Science Fund FWF W 1226
6 · The paper itself

Abstract

The importance of peroxisomes for adipocyte function is poorly understood. Herein, we provide insights into the critical role of peroxin 16 (PEX16)-mediated peroxisome biogenesis in adipocyte development and lipid metabolism. Pex16 is highly expressed in adipose tissues and upregulated during adipogenesis of murine and human cells. We demonstrate that Pex16 is a target gene of the adipogenesis "master-regulator" PPARγ. Stable silencing of Pex16 in 3T3-L1 cells strongly reduced the number of peroxisomes while mitochondrial number was unaffected. Concomitantly, peroxisomal fatty acid (FA) oxidation was reduced, thereby causing accumulation of long- and very long-chain (polyunsaturated) FAs and reduction of odd-chain FAs. Further, Pex16-silencing decreased cellular oxygen consumption and increased FA release. Additionally, silencing of Pex16 impaired adipocyte differentiation, lipogenic and adipogenic marker gene expression, and cellular triglyceride stores. Addition of PPARγ agonist rosiglitazone and peroxisome-related lipid species to Pex16-silenced 3T3-L1 cells rescued adipogenesis. These data provide evidence that PEX16 is required for peroxisome biogenesis and highlights the relevance of peroxisomes for adipogenesis and adipocyte lipid metabolism.

Indexed as

3T3-L1 CellsAdipocytes, WhiteAdipogenesisAnimalsCell DifferentiationCell LineChlorocebus aethiopsCOS CellsFatty AcidsHomeostasisHumansLipid MetabolismLipidsMaleMembrane ProteinsMiceFatty AcidsLipidsMembrane ProteinsPPAR gammaAdipogenesisLipid homeostasisPeroxisomePEX16PPARγ

Identifiers

PMID28017862
PMCPMC7116240
OpenAlexW2562455824

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.