Evidence map›Paper›PMID 32047213›Full record

ArticleScientific reports2020

The Adipocyte Acquires a Fibroblast-Like Transcriptional Signature in Response to a High Fat Diet.

Jessica E C Jones, Nabil Rabhi, Joseph Orofino, Ramya Gamini, Valentina Perissi, Cecile Vernochet, Stephen R Farmer

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
6.6field-weighted citation impact, top 2% 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

49 citing papers in PubMed, 79 citations in OpenAlex.

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  13. Hypoxia signaling in the adipose tissue.Journal of molecular cell biology · 2025
    Review
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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

7 authors at 2 institutions in 1 country.

Jessica E C JonesDepartment of Biochemistry, Boston University School of Medicine, 72 East Concord Street, Boston, MA, 02118, USA.
Nabil RabhiDepartment of Biochemistry, Boston University School of Medicine, 72 East Concord Street, Boston, MA, 02118, USA.
Joseph OrofinoDepartment of Biochemistry, Boston University School of Medicine, 72 East Concord Street, Boston, MA, 02118, USA.
Ramya GaminiInternal Medicine Research Unit, Worldwide Research, Development and Medical, Pfizer Inc, 1 Portland Street, Cambridge, MA, 02139, USA.
Valentina PerissiDepartment of Biochemistry, Boston University School of Medicine, 72 East Concord Street, Boston, MA, 02118, USA.
Cecile VernochetInternal Medicine Research Unit, Worldwide Research, Development and Medical, Pfizer Inc, 1 Portland Street, Cambridge, MA, 02139, USA.
Stephen R FarmerDepartment of Biochemistry, Boston University School of Medicine, 72 East Concord Street, Boston, MA, 02118, USA. sfarmer@bu.edu.
Boston University · USPfizer (United States) · US

Funding

Transgenic CoreP30DK046200 · NIDDK · TUFTS MEDICAL CENTER · PI GREENBERG, ANDREW S, PERISSI, VALENTINA · 1992 to 2021
$25.0M
Healthy Remodeling of Obese Adipose TissueR01DK117161 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FARMER, STEPHEN ROBERT · 2018 to 2021
$1.9M
Ubiquitin-dependent regulation of inflammation and insulin resistanceR01DK100422 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI PERISSI, VALENTINA · 2014 to 2018
$1.8M
Regulation of mitochondrial homeostasis through retrograde signalingR01GM127625 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI PERISSI, VALENTINA · 2018 to 2021
$1.8M
Therapeutic strategies to induce browning of white adipose tissueR01DK117163 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FARMER, STEPHEN ROBERT · 2019 to 2021
$1.2M
NIDDK NIH HHS P30 DK046200NIDDK NIH HHS R01 DK100422NIDDK NIH HHS R01 DK117161NIDDK NIH HHS R01 DK117163NIGMS NIH HHS R01 GM127625
6 · The paper itself

Abstract

Visceral white adipose tissue (vWAT) expands and undergoes extensive remodeling during diet-induced obesity. Much is known about the contribution of various stromal vascular cells to the remodeling process, but less is known of the changes that occur within the adipocyte as it becomes progressively dysfunctional. Here, we performed a transcriptome analysis of isolated vWAT adipocytes to assess global pathway changes occurring in response to a chronic high fat diet (HFD). The data demonstrate that the adipocyte responds to the HFD by adopting a fibroblast-like phenotype, characterized by enhanced expression of ECM, focal adhesion and cytoskeletal genes and suppression of many adipocyte programs most notably those associated with mitochondria. This study reveals that during obesity the adipocyte progressively becomes metabolically dysfunctional due to its acquisition of fibrogenic functions. We propose that mechano-responsive transcription factors such as MRTFA and SRF contribute to both upregulation of morphological genes as well as suppression of mitochondrial programs.

Indexed as

TranscriptomeAdipocytes, WhiteAnimalsDiet, High-FatExtracellular Matrix ProteinsFibroblastsIntra-Abdominal FatMaleMiceMice, Inbred C57BLExtracellular Matrix Proteins

Identifiers

PMID32047213
PMCPMC7012923
OpenAlexW3005933224

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.