Cited by 135Adipose Tissue and MetabolismPeroxisome Proliferator-Activated ReceptorsAdipokines, Inflammation, and Metabolic Diseases

Distinct cellular and molecular mechanisms for β3 adrenergic receptor-induced beige adipocyte formation

Open access
Jiang, Yuwei, Berry, Daniel C, Graff, Jonathan M·2017·eLife

Abstract

Beige/brite adipocytes are induced within white adipose tissues (WAT) and, when activated, consume glucose and fatty acids to produce heat. Classically, two stimuli have been used to trigger a beiging response: cold temperatures and β3-adrenergic receptor (Adrb3) agonists. These two beiging triggers have been used interchangeably but whether these two stimuli may induce beiging differently at cellular and molecular levels remains unclear. Here, we found that cold-induced beige adipocyte formation requires Adrb1, not Adrb3, activation. Adrb1 activation stimulates WAT resident perivascular (Acta2+) cells to form cold-induced beige adipocytes. In contrast, Adrb3 activation stimulates mature white adipocytes to convert into beige adipocytes. Necessity tests, using mature adipocyte-specific Prdm16 deletion strategies, demonstrated that adipocytes are required and are predominant source to generate Adrb3-induced, but not cold-induced, beige adipocytes. Collectively, we identify that cold temperatures and Adrb3 agonists activate distinct cellular populations that express different β-adrenergic receptors to induce beige adipogenesis.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.7554/elife.30329

Cites

58 of 58 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • ADRB3 is the key mediator for the stimulatory effects of catecholamines on WAT lipolysis and BAT thermogenesis.

    “ADRB3 is the key mediator for the stimulatory effects of catecholamines on WAT lipolysis and BAT thermogenesis (Claustre et al, 2008; Jiang et al, 2017).”

    From Exercise‐induced α‐ketoglutaric acid stimulates muscle hypertrophy and fat loss through OXGR1‐dependent adrenal activation (2020) · cites this paper as Jiang et al, 2017

    The Introduction (page unavailable) says norepinephrine signals through Adrb3 to stimulate thermogenic action in mature brown adipocytes. It does not identify Adrb3 as the key mediator of catecholamine-stimulated WAT lipolysis; the Results (page unavailable) report reduced triglycerides after treatment with an Adrb3 agonist, but do not establish that broader claim. (LLM, conf=0.85)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Jiang, Y., Berry, D. C., & Graff, J. M.
Affiliations
  • The University of Texas Southwestern Medical Center (US)
  • Cornell University (US)
Corresponding author
  • Berry, Daniel C
  • Graff, Jonathan M
Venue
eLife
Published
2017-10-11
Volume
6
ISSN
2050-084X (ISSN-L)
OpenAlex
W2763289003
Cited by
135
References
58
Citations by year
2026: 7 · 2025: 12 · 2024: 15 · 2023: 17 · 2022: 19 · 2021: 21 · 2020: 22 · 2019: 14 · 2018: 6 · 2017: 2
FWCI
8.90
Type
journal article
Language
en
Open access
Locations
  • eLife (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
National Institute of Diabetes and Digestive and Kidney Diseases (K01 DK109027, K01 DK111771, R01 DK088220, R01 DK064261, R01 DK066556)
Topics
  • Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
  • Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
Keywords
beige adipocytes, beta3-adrenergic receptor, ADRB1, white adipose tissue, perivascular cells, PRDM16, adipogenesis, thermogenesis
MeSH terms
Adipocytes, Beige, Animals, Cell Differentiation, Cold Temperature, Mice, Inbred C57BL, Receptors, Adrenergic, beta-1, Receptors, Adrenergic, beta-3

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review