Evidence map›Paper›PMID 36109558›Full record

ArticleNature communications2022

Liver group 2 innate lymphoid cells regulate blood glucose levels through IL-13 signaling and suppression of gluconeogenesis.

Masanori Fujimoto, Masataka Yokoyama, Masahiro Kiuchi, Hiroyuki Hosokawa, Akitoshi Nakayama, Naoko Hashimoto, Ikki Sakuma, Hidekazu Nagano, Kazuyuki Yamagata, Fujimi Kudo and 9 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

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  10. Group 2 innate lymphoid cells suppress neuroinflammation and brain injury following intracerebral hemorrhage.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2024
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  11. (Multi-) omics studies of ILC2s in inflammation and metabolic diseases.Frontiers in cell and developmental biology · 2024
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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

19 authors at 2 institutions in 1 country.

Masanori FujimotoDepartment of Molecular Diagnosis, Graduate School of Medicine, Chiba University, Chiba, Japan.
Masataka YokoyamaDepartment of Molecular Diagnosis, Graduate School of Medicine, Chiba University, Chiba, Japan.
Masahiro KiuchiDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Hiroyuki HosokawaDepartment of Immunology, Tokai University School of Medicine, Isehara, Kanagawa, Japan.ORCID 0000-0002-9592-2889
Akitoshi NakayamaDepartment of Molecular Diagnosis, Graduate School of Medicine, Chiba University, Chiba, Japan.
Naoko HashimotoDepartment of Molecular Diagnosis, Graduate School of Medicine, Chiba University, Chiba, Japan.
Ikki SakumaDepartment of Molecular Diagnosis, Graduate School of Medicine, Chiba University, Chiba, Japan.
Hidekazu NaganoDepartment of Molecular Diagnosis, Graduate School of Medicine, Chiba University, Chiba, Japan.
Kazuyuki YamagataDepartment of Molecular Diagnosis, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0002-5804-6090
Fujimi KudoDepartment of Systems Medicine, Graduate School of Medicine, Chiba University, Chiba, Japan.
Ichiro ManabeDepartment of Systems Medicine, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0001-9481-6673
Eunyoung LeeDepartment of Medical Physiology, Chiba University, Graduate School of Medicine, Chiba, Japan.
Ryo HatanoDepartment of Medical Physiology, Chiba University, Graduate School of Medicine, Chiba, Japan.
Atsushi OnoderaDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Kiyoshi HiraharaDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0002-9128-9449
Koutaro YokoteDepartment of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Takashi MikiDepartment of Medical Physiology, Chiba University, Graduate School of Medicine, Chiba, Japan.ORCID 0000-0001-5741-1626
Toshinori NakayamaDepartment of Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID 0000-0002-1434-2007
Tomoaki TanakaDepartment of Molecular Diagnosis, Graduate School of Medicine, Chiba University, Chiba, Japan. tomoaki@restaff.chiba-u.jp.ORCID 0000-0002-9761-1750
Chiba University · JPTokai University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The liver stores glycogen and releases glucose into the blood upon increased energy demand. Group 2 innate lymphoid cells (ILC2) in adipose and pancreatic tissues are known for their involvement in glucose homeostasis, but the metabolic contribution of liver ILC2s has not been studied in detail. Here we show that liver ILC2s are directly involved in the regulation of blood glucose levels. Mechanistically, interleukin (IL)-33 treatment induces IL-13 production in liver ILC2s, while directly suppressing gluconeogenesis in a specific Hnf4a/G6pc-high primary hepatocyte cluster via Stat3. These hepatocytes significantly interact with liver ILC2s via IL-13/IL-13 receptor signaling. The results of transcriptional complex analysis and GATA3-ChIP-seq, ATAC-seq, and scRNA-seq trajectory analyses establish a positive regulatory role for the transcription factor GATA3 in IL-13 production by liver ILC2s, while AP-1 family members are shown to suppress IL-13 release. Thus, we identify a regulatory role and molecular mechanism by which liver ILC2s contribute to glucose homeostasis.

Indexed as

GluconeogenesisInterleukin-13Blood GlucoseGATA3 Transcription FactorGlycogenImmunity, InnateLiverLymphocytesReceptors, Interleukin-13Transcription Factor AP-1Blood GlucoseGATA3 Transcription FactorGlycogenInterleukin-13Receptors, Interleukin-13Transcription Factor AP-1

Identifiers

PMID36109558
PMCPMC9478157
OpenAlexW4296028813

What OpenQuestion holds

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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.