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Integrated single-cell RNA-seq and DNA methylation reveal the effects of air pollution in patients with recurrent spontaneous abortion.

Authors :
Zhu, Weiqiang
Gu, Yan
Li, Min
Zhang, Zhaofeng
Liu, Junwei
Mao, Yanyan
Zhu, Qianxi
Zhao, Lin
Shen, Yupei
Chen, Fujia
Xia, Lingjin
He, Lin
Du, Jing
Source :
Clinical Epigenetics; 8/23/2022, Vol. 14 Issue 1, p1-17, 17p
Publication Year :
2022

Abstract

Background: Maternal air pollutants exposure is associated with a number of adverse pregnancy outcomes, including recurrent spontaneous abortion (RSA). However, the underlying mechanisms are still unknown. The present study aimed to understand the mechanism of RSA and its relationship with air pollution exposure. We compared data of decidual tissue from individuals with induced abortions and those with RSA by bulk RNA sequencing (RNA-seq), reduced representation bisulfite sequencing (RRBS), and single-cell RNA sequencing (scRNA-seq). Differentially expressed genes (DEGs) were verified using RT-qPCR and pyrosequencing. A logistic regression model was used to investigate the association between air pollutants exposure and RSA. Results: We identified 98 DEGs with aberrant methylation by overlapping the RRBS and RNA-seq data. Nineteen immune cell subsets were identified. Compared with normal controls, NK cells and macrophages accounted for different proportions in the decidua of patients with RSA. We observed that the methylation and expression of IGF2BP1 were different between patients with RSA and controls. Furthermore, we observed significant positive associations between maternal air pollutants exposure during the year prior to pregnancy and in early pregnancy and the risk of RSA. Mediation analyses suggested that 24.5% of the effects of air pollution on the risk of RSA were mediated through IGF2BP1 methylation. Conclusion: These findings reveal a comprehensive cellular and molecular mechanism of RSA and suggest that air pollution might cause pregnancy loss by affecting the methylation level of the IGF2BP1 promoter. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18687075
Volume :
14
Issue :
1
Database :
Complementary Index
Journal :
Clinical Epigenetics
Publication Type :
Academic Journal
Accession number :
158670528
Full Text :
https://doi.org/10.1186/s13148-022-01327-2