Evidence map›Paper›PMID 33148324›Full record

ArticleStem cell research & therapy2020

hPMSCs protects against D-galactose-induced oxidative damage of CD4

Yanlian Xiong, Yueming Wang, Jiashen Zhang, Nannan Zhao, Hengchao Zhang, Aiping Zhang, Dongmei Zhao, Zhenhai Yu, Yancun Yin, Lele Song and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 11% 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, 29 citations in OpenAlex.

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  8. Potential role of mesenchymal stem cells in T cell aging.Journal of molecular medicine (Berlin, Germany) · 2023
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Yanlian XiongDepartment of Anatomy, School of Basic Medicine, Binzhou Medical University, Yantai, People's Republic of China.
Yueming WangDepartment of Anatomy, School of Basic Medicine, Binzhou Medical University, Yantai, People's Republic of China.
Jiashen ZhangDepartment of Immunology, School of Basic Medicine, Binzhou Medical University, Yantai, People's Republic of China.
Nannan ZhaoDepartment of Immunology, School of Basic Medicine, Binzhou Medical University, Yantai, People's Republic of China.
Hengchao ZhangDepartment of Immunology, School of Basic Medicine, Binzhou Medical University, Yantai, People's Republic of China.
Aiping ZhangDepartment of Immunology, School of Basic Medicine, Binzhou Medical University, Yantai, People's Republic of China.
Dongmei ZhaoDepartment of Anatomy, School of Basic Medicine, Binzhou Medical University, Yantai, People's Republic of China.
Zhenhai YuDepartment of Anatomy, School of Basic Medicine, Binzhou Medical University, Yantai, People's Republic of China.
Yancun YinDepartment of Anatomy, School of Basic Medicine, Binzhou Medical University, Yantai, People's Republic of China.
Lele SongDepartment of Immunology, School of Basic Medicine, Binzhou Medical University, Yantai, People's Republic of China.
Yanlei XiongDepartment of Pathology, Xuanwu Hospital, Capital Medical University, Beijing, People's Republic of China. xiongyanlei@sina.com.
Xiying LuanDepartment of Immunology, School of Basic Medicine, Binzhou Medical University, Yantai, People's Republic of China. xiying_luan@163.com.
Binzhou Medical University · CNBinzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMesenchymal stem cells (MSCs) were considered a regenerative therapeutic approach in both acute and chronic diseases. However, whether MSCs regulate the antioxidant metabolism of CD4

methodsIn vivo study, 40 male C57BL/6 mice (8 weeks) were randomly divided into four groups: control group, D-gal group, hPMSC group, and PBS group. In in vitro experiment, human naive CD4

resultsWe found that hPMSC treatment markedly decreased the ROS level, SA-β-gal-positive cells number, senescence-associated secretory phenotype (IL-6 and OPN) expression, and aging-related protein (P16 and P21) expression in senescent CD4

conclusionsOur results indicate that hPMSCs attenuate D-gal-induced CD4

Indexed as

AntioxidantsNF-E2-Related Factor 2AnimalsCD4-Positive T-LymphocytesGalactoseGlycogen Synthase Kinase 3 betaMaleMiceMice, Inbred C57BLOxidative StressProto-Oncogene Proteins c-aktT-LymphocytesAntioxidantsGalactoseGlycogen Synthase Kinase 3 betaNF-E2-Related Factor 2Proto-Oncogene Proteins c-aktAgingCD4+ T cellshPMSCNrf2Oxidative stressSenescence-associated secretoryphenotype

Identifiers

PMID33148324
PMCPMC7641865
OpenAlexW3094916725

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.