Evidence map›Paper›PMID 29463855›Full record

ArticleScientific reports2018

Zearalenone altered the cytoskeletal structure via ER stress- autophagy- oxidative stress pathway in mouse TM4 Sertoli cells.

Wanglong Zheng, Bingjie Wang, Mengxue Si, Hui Zou, Ruilong Song, Jianhong Gu, Yan Yuan, Xuezhong Liu, Guoqiang Zhu, Jianfa Bai and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. 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 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.6field-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

32 citing papers in PubMed, 89 citations in OpenAlex.

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  16. Chemerin regulates autophagy to participate in polycystic ovary syndrome.The Journal of international medical research · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 3 countries.

Wanglong ZhengCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Bingjie WangCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Mengxue SiCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Hui ZouCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Ruilong SongCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Jianhong GuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Yan YuanCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Xuezhong LiuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Guoqiang ZhuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Jianfa BaiKansas State Veterinary Diagnostic Laboratory, Kansas State University, 1800 Denison Avenue, Manhattan, KS, 66506, United States.ORCID http://orcid.org/0000-0002-0021-3036
Jianchun BianCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China. jcbian@yzu.edu.cn.
ZongPing LiuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China. liuzongping@yzu.edu.cn.
Jiangsu Provincial Center for Disease Control and Prevention · CNKansas State University · USMinistry of Education · MV

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to investigate the molecular mechanisms of the destruction of cytoskeletal structure by Zearalenone (ZEA) in mouse-derived TM4 cells. In order to investigate the role of autophagy, oxidative stress and endoplasmic reticulum(ER) stress in the process of destruction of cytoskeletal structure, the effects of ZEA on the cell viability, cytoskeletal structure, autophagy, oxidative stress, ER stress, MAPK and PI3K- AKT- mTOR signaling pathways were studied. The data demonstrated that ZEA damaged the cytoskeletal structure through the induction of autophagy that leads to the alteration of cytoskeletal structure via elevated oxidative stress. Our results further showed that the autophagy was stimulated by ZEA through PI3K-AKT-mTOR and MAPK signaling pathways in TM4 cells. In addition, ZEA also induced the ER stress which was involved in the induction of the autophagy through inhibiting the ERK signal pathway to suppress the phosphorylation of mTOR. ER stress was involved in the damage of cytoskeletal structure through induction of autophagy by producing ROS. Taken together, this study revealed that ZEA altered the cytoskeletal structure via oxidative stress - autophagy- ER stress pathway in mouse TM4 Sertoli cells.

Indexed as

AutophagyEndoplasmic Reticulum StressOxidative StressAnimalsCells, CulturedCell SurvivalCytoskeletonEstrogens, Non-SteroidalGene Expression RegulationMaleMiceMitogen-Activated Protein KinasesPhosphatidylinositol 3-KinasesPhosphorylationProto-Oncogene Proteins c-aktSertoli CellsAkt1 protein, mouseEstrogens, Non-SteroidalMitogen-Activated Protein KinasesmTOR protein, mousePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesZearalenone

Identifiers

PMID29463855
PMCPMC5820275
OpenAlexW2806977025

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.