Evidence map›Paper›PMID 27562191›Full record

ArticleThe Journal of endocrinology2016

IL-33-driven ILC2/eosinophil axis in fat is induced by sympathetic tone and suppressed by obesity.

Xiaofeng Ding, Yan Luo, Xing Zhang, Handong Zheng, Xin Yang, Xuexian Yang, Meilian Liu

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

62 citing papers in PubMed, 92 citations in OpenAlex.

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  17. From fasting to fat reshaping: exploring the molecular pathways of intermittent fasting-induced adipose tissue remodeling.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2024
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2 more citing papers are in PubMed but not listed here.

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 3 institutions in 2 countries.

Xiaofeng DingDepartment of Biochemistry and Molecular BiologyUniversity of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA Key Laboratory of Protein Chemistry and Development Biology of State Education Ministry of ChinaCollege of Life Science, Hunan Normal University, Changsha, Hunan, China.
Yan LuoDepartment of Biochemistry and Molecular BiologyUniversity of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA Department of Metabolism and EndocrinologyMetabolic Syndrome Research Center, Key Laboratory of Diabetes Immunology, Ministry of Education, National Clinical Research Center for Metabolic Diseases, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xing ZhangDepartment of Biochemistry and Molecular BiologyUniversity of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA Department of Molecular Genetics and MicrobiologyUniversity of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA.
Handong ZhengDepartment of Molecular Genetics and MicrobiologyUniversity of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA.
Xin YangDepartment of Biochemistry and Molecular BiologyUniversity of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA.
Xuexian YangDepartment of Molecular Genetics and MicrobiologyUniversity of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA xyang@salud.unm.edu meilianliu@salud.unm.edu.
Meilian LiuDepartment of Biochemistry and Molecular BiologyUniversity of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA Department of Metabolism and EndocrinologyMetabolic Syndrome Research Center, Key Laboratory of Diabetes Immunology, Ministry of Education, National Clinical Research Center for Metabolic Diseases, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China xyang@salud.unm.edu meilianliu@salud.unm.edu.
University of New Mexico · USSecond Xiangya Hospital of Central South University · CNHunan Normal University · CN

Funding

WOMEN'S CANCERS RESEARCH PROGRAMP30CA118100 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Yolanda Sanchez · 2005 to 2026
$57.1M
Integrative Program in CNS Pathophysiology ResearchP30GM103400 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI LIU, KE JIAN · 2012 to 2016
$4.7M
NCI NIH HHS P30 CA118100NIAID NIH HHS HHSN272201300006CNIGMS NIH HHS P30 GM103400
6 · The paper itself

Abstract

Group 2 innate lymphoid cells (ILC2s) in white adipose tissue (WAT) promote WAT browning and assist in preventing the development of obesity. However, how ILC2 in adipose tissue is regulated remains largely unknown. Here, our study shows that ILC2s are present in brown adipose tissue (BAT) as well as subcutaneous and epididymal WAT (sWAT and eWAT). The fractions of ILC2s, natural killer T (NKT) cells and eosinophils in sWAT, eWAT and BAT are significantly decreased by high-fat-diet (HFD) feeding and leptin deficiency-induced obesity. Consistent with this, the adipose expression and circulating levels of IL-33, a key inducing cytokine of ILC2, are significantly downregulated by obesity. Furthermore, administration of IL-33 markedly increases the fraction of ILC2 and eosinophil as well as the expression of UCP1 and tyrosine hydroxylase (TH), a rate-limiting enzyme in catecholamine biosynthesis, in adipose tissue of HFD-fed mice. On the other hand, cold exposure induces the expression levels of IL-33 and UCP1 and the population of ILC2 and eosinophil in sWAT, and these promoting effects of cold stress are reversed by neutralization of IL-33 signaling in vivo Moreover, the basal and cold-induced IL-33 and ILC2/eosinophil pathways are significantly suppressed by sympathetic denervation via local injection of 6-hydroxydopamine (6-OHDA) in sWAT. Taken together, our data suggest that the ILC2/eosinophil axis in adipose tissue is regulated by sympathetic nervous system and obesity in IL-33-dependent manner, and IL-33-driven ILC2/eosinophil axis is implicated in the development of obesity.

Indexed as

Adipose Tissue, BrownAdipose Tissue, WhiteAnimalsDiet, High-FatEosinophilsImmunity, InnateInterleukin-33LymphocytesMaleMiceObesityInterleukin-33eosinophilIL-33ILC2obesitysympathetic tone

Identifiers

PMID27562191
PMCPMC5003423
OpenAlexW2514976730

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.