Evidence map›Paper›PMID 37429951›Full record

ArticleNature aging2023

Cxxc finger protein 1 maintains homeostasis and function of intestinal group 3 innate lymphoid cells with aging.

Xin Shen, Xianzhi Gao, Yikai Luo, Qianying Xu, Ying Fan, Shenghui Hong, Zhengwei Huang, Xiaoqian Liu, Qianqian Wang, Zuojia Chen and 5 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Nature aging, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

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  11. Immune aging and infectious diseases.Chinese medical journal · 2024
    Review
  12. Review
  13. Review
  14. Group 3 innate lymphoid cells in intestinal health and disease.Nature reviews. Gastroenterology & hepatology · 2024
    Review
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

15 authors at 5 institutions in 3 countries.

Xin Shen *Institute of Immunology and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xianzhi Gao *Institute of Immunology and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yikai Luo *Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0001-7589-7981
Qianying XuZhejiang University School of Medicine, Hangzhou, China.
Ying FanLaboratory Animal Center, Zhejiang University, Hangzhou, China.
Shenghui HongLaboratory Animal Center, Zhejiang University, Hangzhou, China.
Zhengwei HuangZhejiang University School of Medicine, Hangzhou, China.
Xiaoqian LiuInstitute of Immunology and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Qianqian WangLaboratory Animal Center, Zhejiang University, Hangzhou, China.
Zuojia ChenExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Di WangZhejiang University School of Medicine, Hangzhou, China.ORCID http://orcid.org/0000-0002-2712-1705
Linrong LuZhejiang University School of Medicine, Hangzhou, China.
Chuan WuExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. chuan.wu@nih.gov.
Han LiangDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. hliang1@mdanderson.org.ORCID http://orcid.org/0000-0001-7633-286X
Lie WangInstitute of Immunology and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China. wanglie@zju.edu.cn.ORCID http://orcid.org/0000-0001-5094-012X
Zhejiang University · CNZhejiang Chinese Medical University · CNNational Institutes of Health · USThe University of Texas MD Anderson Cancer Center · USFirst Affiliated Hospital Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aging is accompanied by homeostatic and functional dysregulation of multiple immune cell subsets. Group 3 innate lymphoid cells (ILC3s) constitute a heterogeneous cell population that plays pivotal roles in intestinal immunity. In this study, we found that ILC3s in aged mice exhibited dysregulated homeostasis and function, leading to bacterial and fungal infection susceptibility. Moreover, our data revealed that the enrichment of the H3K4me3 modification in effector genes of aged gut CCR6

Indexed as

Immunity, InnateLymphocytesAnimalsCell DifferentiationHomeostasisMiceTrans-ActivatorsCxxc1 protein, mouseTrans-Activators

Identifiers

PMID37429951
OpenAlexW4383814925

What OpenQuestion holds

Textmetadata
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.