Evidence map›Paper›PMID 33878347›Full record

ArticleDevelopmental cell2021

Aging-dependent regulatory cells emerge in subcutaneous fat to inhibit adipogenesis.

Hai P Nguyen, Frances Lin, Danielle Yi, Ying Xie, Jennie Dinh, Pengya Xue, Hei Sook Sul

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
12.4field-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

71 citing papers in PubMed, 124 citations in OpenAlex.

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11 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Hai P NguyenDepartment of Nutritional Sciences & Toxicology, University of California, Berkeley, Berkeley, CA 94720, USA.
Frances LinDepartment of Nutritional Sciences & Toxicology, University of California, Berkeley, Berkeley, CA 94720, USA.
Danielle YiDepartment of Nutritional Sciences & Toxicology, University of California, Berkeley, Berkeley, CA 94720, USA; Endocrinology Program, University of California, Berkeley, Berkeley, CA 94720, USA.
Ying XieDepartment of Nutritional Sciences & Toxicology, University of California, Berkeley, Berkeley, CA 94720, USA.
Jennie DinhDepartment of Nutritional Sciences & Toxicology, University of California, Berkeley, Berkeley, CA 94720, USA.
Pengya XueDepartment of Nutritional Sciences & Toxicology, University of California, Berkeley, Berkeley, CA 94720, USA.
Hei Sook SulDepartment of Nutritional Sciences & Toxicology, University of California, Berkeley, Berkeley, CA 94720, USA; Endocrinology Program, University of California, Berkeley, Berkeley, CA 94720, USA. Electronic address: hsul@berkeley.edu.
University of California, Berkeley · US

Funding

Brown adipose NADH oxidase for thermogenesisR01DK123843 · NIDDK · UNIVERSITY OF CALIFORNIA BERKELEY · PI SUL, HEI SOOK · 2020 to 2023
$2.4M
Role of B2 in Brown Fat Transcription and DevelopmentR01DK095338 · NIDDK · UNIVERSITY OF CALIFORNIA BERKELEY · PI SUL, HEI SOOK · 2012 to 2016
$1.8M
A Zeiss LSM 710 confocal microscope for the Biological Imaging Facility at the US10RR026866 · NCRR · UNIVERSITY OF CALIFORNIA BERKELEY · PI RUZIN, STEVEN EARL · 2010 to 2010
$419k
NCRR NIH HHS S10 RR026866NIDDK NIH HHS R01 DK095338NIDDK NIH HHS R01 DK123843
6 · The paper itself

Abstract

Adipose tissue mass and adiposity change throughout the lifespan. During aging, while visceral adipose tissue (VAT) tends to increase, peripheral subcutaneous adipose tissue (SAT) decreases significantly. Unlike VAT, which is linked to metabolic diseases, including type 2 diabetes, SAT has beneficial effects. However, the molecular details behind the aging-associated loss of SAT remain unclear. Here, by comparing scRNA-seq of total stromal vascular cells of SAT from young and aging mice, we identify an aging-dependent regulatory cell (ARC) population that emerges only in SAT of aged mice and humans. ARCs express adipose progenitor markers but lack adipogenic capacity; they secrete high levels of pro-inflammatory chemokines, including Ccl6, to inhibit proliferation and differentiation of neighboring adipose precursors. We also found Pu.1 to be a driving factor for ARC development. We identify an ARC population and its capacity to inhibit differentiation of neighboring adipose precursors, correlating with aging-associated loss of SAT.

Indexed as

Adipogenesis3T3-L1 CellsAdipocytesAgingAnimalsCD36 AntigensCell ProliferationChemokinesGalectin 3MiceProto-Oncogene ProteinsProto-Oncogene Protein Spi-1Stem CellsSubcutaneous FatTrans-ActivatorsCD36 AntigensChemokinesGalectin 3Lgals3 protein, mouseProto-Oncogene ProteinsProto-Oncogene Protein Spi-1Trans-Activatorsadipogenesisadipose precursorsadipose tissueagingsubcutaneous adipose tissue

Identifiers

PMID33878347
PMCPMC8137669
OpenAlexW3152652982

What OpenQuestion holds

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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.