Oct4 plays a role in 2, 3, 7, 8 - tetrachlorobenzo-p-dioxin (TCDD) inducing cleft palate and inhibiting mesenchymal proliferation.


Journal

Toxicology
ISSN: 1879-3185
Titre abrégé: Toxicology
Pays: Ireland
ID NLM: 0361055

Informations de publication

Date de publication:
30 05 2020
Historique:
received: 06 12 2019
revised: 17 03 2020
accepted: 25 03 2020
pubmed: 14 4 2020
medline: 1 9 2020
entrez: 14 4 2020
Statut: ppublish

Résumé

As a common birth defect, Cleft palate can be caused by the disturbance during the developmental process of the palatal shelves. The 2,3,7,8-tetrachlorodibenzo- p-dioxin (TCDD) is a well-known environmental teratogenic agent for cleft palate and Aryl hydrocarbon receptor (AhR) pathway can be activated by dioxins. Oct4 as a pluripotent stem cell transcription factor is also involved in the process of embryonic development. The AHR and retinoid receptors have cross-talk at CYP1A1 (cytochrome P450, family 1, subfamily A, polypeptide 1) promoter. There are also bidirectional talk between AhR and Oct4. In this study, we used C57/BL6 N mice and TCDD (64 μg/Kg body weight) to establish a model of fetal cleft palate to observe the effects of dioxin on fetal mesenchymal proliferation and apoptosis, and explore the role of Oct4 in inducing cleft palate. The results showed that dioxin inhibited mesenchymal proliferation and promoted apoptosis. In addition, dioxin inhibited Oct4 expression, and preliminary data suggest that hypermethylation of the Oct4 promoter may be a putative mechanism, suggesting that TCDD might induce cleft palate by inhibiting the proliferation of palatal mesenchymal cells mediated by Oct4.

Identifiants

pubmed: 32283119
pii: S0300-483X(20)30083-4
doi: 10.1016/j.tox.2020.152444
pii:
doi:

Substances chimiques

Ahr protein, mouse 0
Basic Helix-Loop-Helix Transcription Factors 0
Octamer Transcription Factor-3 0
Polychlorinated Dibenzodioxins 0
Pou5f1 protein, mouse 0
Receptors, Aryl Hydrocarbon 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

152444

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Yuchang Tao (Y)

School of Public Health, Zhengzhou University, No. 100 of Science Road, Zhengzhou, 450001, China.

Xiaozhuan Liu (X)

Center for Clinical Single-Cell Biomedicine, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, No. 7 of Weiwu Road, Zhengzhou, 450001, China.

Lingling Cui (L)

School of Public Health, Zhengzhou University, No. 100 of Science Road, Zhengzhou, 450001, China.

Xinxin Liu (X)

School of Public Health, Zhengzhou University, No. 100 of Science Road, Zhengzhou, 450001, China.

Yao Chen (Y)

School of Public Health, Zhengzhou University, No. 100 of Science Road, Zhengzhou, 450001, China.

Zhidong He (Z)

School of Public Health, Zhengzhou University, No. 100 of Science Road, Zhengzhou, 450001, China.

Mengmeng Ji (M)

School of Public Health, Zhengzhou University, No. 100 of Science Road, Zhengzhou, 450001, China.

Zhan Gao (Z)

The Fifth Affiliated Hospital of Zhengzhou University, No. 3 of Kangfu Front Street, Zhengzhou, 450052, China.

Ning Li (N)

Henan Agricultural University, No. 63 of Agricultural Road, Zhengzhou, 450002, China.

Zhongxiao Wan (Z)

School of Public Health, Zhengzhou University, No. 100 of Science Road, Zhengzhou, 450001, China. Electronic address: zhongxiaowan1983@163.com.

Zengli Yu (Z)

School of Public Health, Zhengzhou University, No. 100 of Science Road, Zhengzhou, 450001, China. Electronic address: zly@zzu.edu.cn.

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Classifications MeSH