Evidence map›Paper›PMID 30100246›Full record

ArticleMolecular metabolism2018

TGF-β receptor 1 regulates progenitors that promote browning of white fat.

Umesh D Wankhade, Ji-Hyeon Lee, Pradeep K Dagur, Hariom Yadav, Michael Shen, Weiping Chen, Ashok B Kulkarni, J Philip McCoy, Toren Finkel, Aaron M Cypess and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

34 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
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  12. Brown Adipose Tissue Activation in Humans Increases Plasma Levels of Lipid Mediators.The Journal of clinical endocrinology and metabolism · 2024
    Article
  13. Association of Obesity and Severe Asthma in Adults.Journal of clinical medicine · 2024
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Asthma and obesity: endotoxin another insult to add to injury?Clinical science (London, England : 1979) · 2021
    Review
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

11 authors at 3 institutions in 1 country.

Umesh D WankhadeDiabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes & Digestive & Kidney Diseases, USA.
Ji-Hyeon LeeDiabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes & Digestive & Kidney Diseases, USA.
Pradeep K DagurFlow Cytometry Core, National Heart, Lung, and Blood Institute, USA.
Hariom YadavDiabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes & Digestive & Kidney Diseases, USA.
Michael ShenDiabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes & Digestive & Kidney Diseases, USA.
Weiping ChenGenomics Core, National Institute of Diabetes & Digestive & Kidney Diseases, USA.
Ashok B KulkarniFunctional Genomics Section, Laboratory of Cell and Developmental Biology, National Institute of Dental and Craniofacial Research, National Institutes of Health, Clinical Research Center, South Drive and Old Georgetown Road, Bethesda, MD 20892, USA.
J Philip McCoyFlow Cytometry Core, National Heart, Lung, and Blood Institute, USA.
Toren FinkelCenter for Molecular Medicine, National Heart, Lung, and Blood Institute, USA.
Aaron M CypessDiabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes & Digestive & Kidney Diseases, USA.
Sushil G RaneDiabetes, Endocrinology, and Obesity Branch, National Institute of Diabetes & Digestive & Kidney Diseases, USA. Electronic address: ranes@mail.nih.gov.
National Institute of Diabetes and Digestive and Kidney Diseases · USNational Heart Lung and Blood Institute · USNational Institutes of Health · US

Funding

Flow Cytometry Core FacilityZICHL005905 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI DAGUR, PRADEEP · 2009 to 2025
$32.3M
Molecular Roles of Cdk5 in Neuronal Functions and Pain SignalingZIADE000664 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI KULKARNI, ASHOK · 2009 to 2025
$20.4M
Cell Cycle Regulators in Diabetes and ObesityZIADK055107 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI RANE, SUSHIL · 2009 to 2025
$8.4M
Transforming Growth Factor - Beta Superfamily Signaling in Diabetes and ObesityZIADK055106 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI RANE, SUSHIL · 2009 to 2021
$5.7M
The Molecular, Cellular, and Genetic characterization of Human Adipose Tissue and its Role in MetabolismZIADK075112 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI CYPESS, AARON · 2015 to 2025
$2.8M
Mechanisms Underlying Adipose Tissue ThermogenesisZIADK075115 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI CYPESS, AARON · 2015 to 2025
$1.8M
Intramural NIH HHS ZIA DK055106
6 · The paper itself

Abstract

objectiveBeige/brite adipose tissue displays morphological characteristics and beneficial metabolic traits of brown adipose tissue. Previously, we showed that TGF-β signaling regulates the browning of white adipose tissue. Here, we inquired whether TGF-β signals regulated presumptive beige progenitors in white fat and investigated the TGF-β regulated mechanisms involved in beige adipogenesis.

methodsWe deleted TGF-β receptor 1 (TβRI) in adipose tissue (TβRI

resultsDeletion of TβRI promotes beige adipogenesis while reducing the detrimental effects of high fat diet feeding. Interaction of TGF-β signaling with the prostaglandin pathway regulated the appearance of beige adipocytes in white fat. Using flow cytometry techniques and stromal vascular fraction from white fat, we isolated presumptive beige stem/progenitor cells (iBSCs). Upon genetic or pharmacologic inhibition of TGF-β signaling, these cells express high levels of predominantly beige markers. Transplantation of TβRI-deficient stromal vascular cells or iBSCs into athymic nude mice followed by high fat diet feeding and stimulation of β-adrenergic signaling via CL316,243 injection or cold exposure promoted robust beige adipogenesis in vivo.

conclusionsTβRI signals target the prostaglandin network to regulate presumptive beige progenitors in white fat capable of developing into beige adipocytes with functional attributes. Controlled inhibition of TβRI signaling and concomitant PGE2 stimulation has the potential to promote beige adipogenesis and improve metabolism.

Indexed as

Adipocytes, BeigeAdipocytes, BrownAdipocytes, WhiteAdipogenesisAdipose Tissue, BeigeAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsCell DifferentiationDiet, High-FatMaleMiceMice, Inbred C57BLMice, KnockoutObesityReceptor, Transforming Growth Factor-beta Type IReceptor, Transforming Growth Factor-beta Type ITgfb1 protein, mouseTransforming Growth Factor beta1Beige/brite adipogenesisCyclooxygenase 2DiabetesMetabolismObesityProgenitorsProstaglandin E2TGF-beta

Identifiers

PMID30100246
PMCPMC6158128
OpenAlexW2883767576

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.