Evidence map›Paper›PMID 26830228›Full record

ArticleMolecular and cellular biology2016

SREBP-1c/MicroRNA 33b Genomic Loci Control Adipocyte Differentiation.

Nathan L Price, Brandon Holtrup, Stephanie L Kwei, Martin Wabitsch, Matthew Rodeheffer, Laurence Bianchini, Yajaira Suárez, Carlos Fernández-Hernando

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. RNA Therapies in Cardio-Kidney-Metabolic Syndrome: Advancing Disease Management.Journal of cardiovascular translational research · 2025
    Review
  3. Review
  4. Review
  5. Review
  6. MicroRNAs as Epigenetic Regulators of Obesity.Advances in experimental medicine and biology · 2024
    Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. MicroRNA-33 Inhibits Adaptive Thermogenesis and Adipose Tissue Beiging.Arteriosclerosis, thrombosis, and vascular biology · 2021
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. HMGA Genes and Proteins in Development and Evolution.International journal of molecular sciences · 2020
    Review
  20. 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

8 authors at 3 institutions in 2 countries.

Nathan L PriceSection of Comparative Medicine, Department of Pathology, Program in Integrative Cell Signaling and Neurobiology of Metabolism and Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, Connecticut, USA Departments of Medicine and Cell Biology, Leon H. Charney Division of Cardiology and Cell Biology, New York University School of Medicine, New York, New York, USA.
Brandon HoltrupSection of Comparative Medicine, Department of Molecular and Cell and Developmental Biology, Program in Integrative Cell Signaling and Neurobiology of Metabolism Program, Yale University School of Medicine, New Haven, Connecticut, USA.
Stephanie L KweiDepartment of Surgery, Section of Plastic and Reconstructive Surgery, Yale University School of Medicine, New Haven, Connecticut, USA.
Martin WabitschDivision of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany.
Matthew RodehefferSection of Comparative Medicine, Department of Molecular and Cell and Developmental Biology, Program in Integrative Cell Signaling and Neurobiology of Metabolism Program, Yale University School of Medicine, New Haven, Connecticut, USA.
Laurence BianchiniLaboratory of Solid Tumors Genetics, Nice University Hospital, Nice, France Institute for Research on Cancer and Aging of Nice (IRCAN), CNRS, UMR 7284/INSERM U1081, University of Nice-Sophia Antiopolis, Nice, France.
Yajaira SuárezSection of Comparative Medicine, Department of Pathology, Program in Integrative Cell Signaling and Neurobiology of Metabolism and Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, Connecticut, USA Departments of Medicine and Cell Biology, Leon H. Charney Division of Cardiology and Cell Biology, New York University School of Medicine, New York, New York, USA.
Carlos Fernández-HernandoSection of Comparative Medicine, Department of Pathology, Program in Integrative Cell Signaling and Neurobiology of Metabolism and Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, Connecticut, USA Departments of Medicine and Cell Biology, Leon H. Charney Division of Cardiology and Cell Biology, New York University School of Medicine, New York, New York, USA carlos.fernandez@yale.edu.
Yale University · USNew York University · USUniversité Côte d'Azur · FR

Funding

Cellular & molecular mechanisms of white adipose tissue mass regulationR01DK090489 · NIDDK · YALE UNIVERSITY · PI RODEHEFFER, MATTHEW S · 2011 to 2020
$3.8M
microRNAs in vascular diseasesR01HL105945 · NHLBI · YALE UNIVERSITY · PI SUAREZ, YAJAIRA · 2011 to 2020
$3.7M
Caveolin-1 in Lipoprotein Metabolism and Atherosclerosis.R01HL106063 · NHLBI · YALE UNIVERSITY · PI FERNANDEZ HERNANDO, CARLOS · 2011 to 2016
$2.5M
Role of microRNAs in lipid metabolism and cardiovascular diseaseR01HL107953 · NHLBI · YALE UNIVERSITY · PI FERNANDEZ HERNANDO, CARLOS · 2011 to 2016
$2.4M
Role of miR-33b in the differentiation and function of white adipose tissueF32DK103489 · NIDDK · YALE UNIVERSITY · PI PRICE, NATHAN · 2014 to 2016
$177k
NHLBI NIH HHS R01 HL105945NHLBI NIH HHS R01HL105945NHLBI NIH HHS R01 HL106063NHLBI NIH HHS R01HL106063NHLBI NIH HHS R01 HL107953NHLBI NIH HHS R01HL107953NIDDK NIH HHS 5F32DK103489-03NIDDK NIH HHS F32 DK103489NIDDK NIH HHS R01 DK090489NIDDK NIH HHS R01DK090489
6 · The paper itself

Abstract

White adipose tissue (WAT) is essential for maintaining metabolic function, especially during obesity. The intronic microRNAs miR-33a and miR-33b, located within the genes encoding sterol regulatory element-binding protein 2 (SREBP-2) and SREBP-1, respectively, are transcribed in concert with their host genes and function alongside them to regulate cholesterol, fatty acid, and glucose metabolism. SREBP-1 is highly expressed in mature WAT and plays a critical role in promoting in vitro adipocyte differentiation. It is unknown whether miR-33b is induced during or involved in adipogenesis. This is in part due to loss of miR-33b in rodents, precluding in vivo assessment of the impact of miR-33b using standard mouse models. This work demonstrates that miR-33b is highly induced upon differentiation of human preadipocytes, along with SREBP-1. We further report that miR-33b is an important regulator of adipogenesis, as inhibition of miR-33b enhanced lipid droplet accumulation. Conversely, overexpression of miR-33b impaired preadipocyte proliferation and reduced lipid droplet formation and the induction of peroxisome proliferator-activated receptor γ (PPARγ) target genes during differentiation. These effects may be mediated by targeting of HMGA2, cyclin-dependent kinase 6 (CDK6), and other predicted miR-33b targets. Together, these findings demonstrate a novel role of miR-33b in the regulation of adipocyte differentiation, with important implications for the development of obesity and metabolic disease.

Indexed as

AdipogenesisAdipose Tissue, WhiteGenetic LociHumansMicroRNAsStem CellsSterol Regulatory Element Binding Protein 1MicroRNAsMIRN33a microRNA, humanSterol Regulatory Element Binding Protein 1

Identifiers

PMID26830228
PMCPMC4800797
OpenAlexW2260443647

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.