Evidence map›Paper›PMID 35848799›Full record

ArticleeLife2022

Deconstructing cold-induced brown adipocyte neogenesis in mice.

Rayanne B Burl, Elizabeth Ann Rondini, Hongguang Wei, Roger Pique-Regi, James G Granneman

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Rayanne B Burl *Center for Molecular Medicine and Genetics, Wayne State University, Detroit, United States.ORCID 0000-0002-3905-4095
Elizabeth Ann Rondini *Center for Molecular Medicine and Genetics, Wayne State University, Detroit, United States.
Hongguang WeiCenter for Molecular Medicine and Genetics, Wayne State University, Detroit, United States.
Roger Pique-RegiCenter for Molecular Medicine and Genetics, Wayne State University, Detroit, United States.ORCID 0000-0002-1262-2275
James G GrannemanCenter for Molecular Medicine and Genetics, Wayne State University, Detroit, United States.ORCID 0000-0001-7013-6630
Wayne State University · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
Analysis of Cellular Plasticity in White Adipose Tissue.R01DK062292 · NIDDK · WAYNE STATE UNIVERSITY · PI James G Granneman · 2003 to 2026
$7.6M
Analysis of Cellular Plasticity in White Adipose TissueR56DK062292 · NIDDK · WAYNE STATE UNIVERSITY · PI GRANNEMAN, JAMES G · 2005 to 2022
$226k
Deconstructing the brown neogenic zone in classic brown adipose tissueF31DK116536 · NIDDK · WAYNE STATE UNIVERSITY · PI BURL, RAYANNE · 2018 to 2020
$112k
NIDDK NIH HHS F31 DK116536NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK062292NIDDK NIH HHS R56 DK062292
6 · The paper itself

Abstract

Cold exposure triggers neogenesis in classic interscapular brown adipose tissue (iBAT) that involves activation of β1-adrenergic receptors, proliferation of PDGFRA+ adipose tissue stromal cells (ASCs), and recruitment of immune cells whose phenotypes are presently unknown. Single-cell RNA-sequencing (scRNA-seq) in mice identified three ASC subpopulations that occupied distinct tissue locations. Of these, interstitial ASC1 were found to be direct precursors of new brown adipocytes (BAs). Surprisingly, knockout of β1-adrenergic receptors in ASCs did not prevent cold-induced neogenesis, whereas pharmacological activation of the β3-adrenergic receptor on BAs was sufficient, suggesting that signals derived from mature BAs indirectly trigger ASC proliferation and differentiation. In this regard, cold exposure induced the delayed appearance of multiple macrophage and dendritic cell populations whose recruitment strongly correlated with the onset and magnitude of neogenesis across diverse experimental conditions. High-resolution immunofluorescence and single-molecule fluorescence in situ hybridization demonstrated that cold-induced neogenesis involves dynamic interactions between ASC1 and recruited immune cells that occur on the micrometer scale in distinct tissue regions. Our results indicate that neogenesis is not a reflexive response of progenitors to β-adrenergic signaling, but rather is a complex adaptive response to elevated metabolic demand within brown adipocytes.

Indexed as

Adipocytes, BrownAdipose Tissue, BrownAnimalsCell DifferentiationIn Situ Hybridization, FluorescenceMiceMice, Inbred C57BLReceptors, Adrenergic, beta-3Receptors, Adrenergic, beta-3adipose stromal cellsbrown adipose tissuecell biologyimmune cellsmouseplasticitysingle-cell RNA-seq

Identifiers

PMID35848799
PMCPMC9348851
OpenAlexW4285729760

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.