Evidence map›Paper›PMID 24609269›Full record

ArticleNature cell biology2014

Visceral and subcutaneous fat have different origins and evidence supports a mesothelial source.

You-Ying Chau, Roberto Bandiera, Alan Serrels, Ofelia M Martínez-Estrada, Wei Qing, Martin Lee, Joan Slight, Anna Thornburn, Rachel Berry, Sophie McHaffie and 5 more

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 308 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
308citing papers in PubMed, 2 pooled it
27.0field-weighted citation impact, top 1% 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

308 citing papers in PubMed, 2 syntheses or guidelines pooled it, 511 citations in OpenAlex.

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  11. PW1Stem cell research & therapy · 2026
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248 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 5 institutions in 2 countries.

You-Ying ChauMedical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine at the University of Edinburgh, Western General Hospital, Crewe Road Edinburgh EH4 2XU, UK.
Roberto BandieraIBV, INSERM U1091, Université de Nice Sophia-Antipolis, Parc Valrose, Centre de Biochimie 06100 Nice Cedex-2, France.
Alan SerrelsInstitute for Genetics and Molecular Medicine at the University of Edinburgh, Edinburgh Cancer Research UK Centre, Western General Hospital Campus, Crewe Road South Edinburgh EH4 2XR, UK.
Ofelia M Martínez-EstradaDepartment of Cell Biology, Faculty of Biology, University of Barcelona, Av. Diagonal, 643 08028 Barcelona, Spain.
Wei QingMedical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine at the University of Edinburgh, Western General Hospital, Crewe Road Edinburgh EH4 2XU, UK.
Martin LeeInstitute for Genetics and Molecular Medicine at the University of Edinburgh, Edinburgh Cancer Research UK Centre, Western General Hospital Campus, Crewe Road South Edinburgh EH4 2XR, UK.
Joan SlightMedical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine at the University of Edinburgh, Western General Hospital, Crewe Road Edinburgh EH4 2XU, UK.
Anna ThornburnMedical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine at the University of Edinburgh, Western General Hospital, Crewe Road Edinburgh EH4 2XU, UK.
Rachel BerryMedical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine at the University of Edinburgh, Western General Hospital, Crewe Road Edinburgh EH4 2XU, UK.
Sophie McHaffieMedical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine at the University of Edinburgh, Western General Hospital, Crewe Road Edinburgh EH4 2XU, UK.
Roland H StimsonBHF Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, Edinburgh EH16 4TJ, UK.
Brian R WalkerBHF Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, Edinburgh EH16 4TJ, UK.
Ramon Muñoz ChapuliDepartment of Animal Biology, University of Málaga, E29071 Málaga, Spain.
Andreas SchedlIBV, INSERM U1091, Université de Nice Sophia-Antipolis, Parc Valrose, Centre de Biochimie 06100 Nice Cedex-2, France.
Nick HastieMedical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine at the University of Edinburgh, Western General Hospital, Crewe Road Edinburgh EH4 2XU, UK.
Western General Hospital · GBThe Queen's Medical Research Institute · GBUniversity of Edinburgh · GBMedical Research Council · GBUniversidad de Málaga · ES

Funding

British Heart Foundation RG/11/4/28734Medical Research Council MC_PC_U127527180Medical Research Council MC_U127527180Medical Research Council MR/K010271/1Medical Research Council U.1275.03.013.00001.01Wellcome TrustWellcome Trust 091374/z/10/z
6 · The paper itself

Abstract

Fuelled by the obesity epidemic, there is considerable interest in the developmental origins of white adipose tissue (WAT) and the stem and progenitor cells from which it arises. Whereas increased visceral fat mass is associated with metabolic dysfunction, increased subcutaneous WAT is protective. There are six visceral fat depots: perirenal, gonadal, epicardial, retroperitoneal, omental and mesenteric, and it is a subject of much debate whether these have a common developmental origin and whether this differs from that for subcutaneous WAT. Here we show that all six visceral WAT depots receive a significant contribution from cells expressing Wt1 late in gestation. Conversely, no subcutaneous WAT or brown adipose tissue arises from Wt1-expressing cells. Postnatally, a subset of visceral WAT continues to arise from Wt1-expressing cells, consistent with the finding that Wt1 marks a proportion of cell populations enriched in WAT progenitors. We show that all visceral fat depots have a mesothelial layer like the visceral organs with which they are associated, and provide several lines of evidence that Wt1-expressing mesothelium can produce adipocytes. These results reveal a major ontogenetic difference between visceral and subcutaneous WAT, and pinpoint the lateral plate mesoderm as a major source of visceral WAT. They also support the notion that visceral WAT progenitors are heterogeneous, and suggest that mesothelium is a source of adipocytes.

Indexed as

AdipocytesAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsAntineoplastic Agents, HormonalCell LineageGene Knock-In TechniquesGreen Fluorescent ProteinsMesodermMiceTamoxifenWT1 ProteinsAntineoplastic Agents, HormonalGreen Fluorescent ProteinsTamoxifenWT1 Proteins

Identifiers

PMID24609269
PMCPMC4060514
OpenAlexW2081513869

What OpenQuestion holds

Textmetadata
LicenceTDM
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.