Evidence map›Paper›PMID 37398933›Full record

ArticleResearch (Washington, D.C.)2023

Cold-Induced Reprogramming of Subcutaneous White Adipose Tissue Assessed by Single-Cell and Single-Nucleus RNA Sequencing.

Qing Liu, Qiaoyun Long, Jiayu Zhao, Wenjie Wu, Zexin Lin, Wei Sun, Ping Gu, Tuo Deng, Kerry Martin Loomes, Donghai Wu and 4 more

Abstract read
In one paragraph

Article in Research (Washington, D.C.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed.

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  8. The DMHAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

14 authors.

Qing LiuSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, China.ORCID https://orcid.org/0000-0003-0258-9755
Qiaoyun LongSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, China.
Jiayu ZhaoDepartment of Pharmacology and Pharmacy, The University of Hong Kong, Hong Kong, China.
Wenjie WuSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, China.
Zexin LinGuangzhou Institute of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Wei SunGuangzhou Institute of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Ping GuDepartment of Endocrinology, Jinling Hospital, Nanjing University, School of Medicine, Nanjing, China.
Tuo DengNational Clinical Research Center for Metabolic Diseases, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, China.
Kerry Martin LoomesSchool of Biological Sciences and Maurice Wilkins Centre, University of Auckland, Auckland, New Zealand.
Donghai WuGuangzhou Institute of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Alice P S KongDepartment of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, China.
Jingying ZhouSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, China.
Alfred S ChengSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, China.
Hannah Xiaoyan HuiSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, China.ORCID https://orcid.org/0000-0002-7525-5812

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adipose browning has demonstrated therapeutic potentials in several diseases. Here, by conducting transcriptomic profiling at the single-cell and single-nucleus resolution, we reconstituted the cellular atlas in mouse inguinal subcutaneous white adipose tissue (iWAT) at thermoneutrality or chronic cold condition. All major nonimmune cells within the iWAT, including adipose stem and progenitor cells (ASPCs), mature adipocytes, endothelial cells, Schwann cells, and smooth muscle cells, were recovered, allowing us to uncover an overall and detailed blueprint for transcriptomes and intercellular cross-talks and the dynamics during white adipose tissue brown remodeling. Our findings also unravel the existence of subpopulations in mature adipocytes, ASPCs, and endothelial cells, as well as new insights on their interconversion and reprogramming in response to cold. The adipocyte subpopulation competent of major histocompatibility complex class II (MHCII) antigen presentation is potentiated. Furthermore, a subcluster of ASPC with CD74 expression was identified as the precursor of this MHCII

Identifiers

PMID37398933
PMCPMC10308956

What OpenQuestion holds

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Registered trials

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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.