4.5 Article

Downregulation of EZH2 in Trophoblasts Induces Decidual M1 Macrophage Polarization: a Potential Cause of Recurrent Spontaneous Abortion

期刊

REPRODUCTIVE SCIENCES
卷 29, 期 10, 页码 2820-2828

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s43032-021-00790-1

关键词

Decidual macrophages; Trophoblast; Enhancer of zeste homolog 2 (EZH2); Polarization; Immune regulation

资金

  1. National Natural Science Foundation of China [81771618, 81971356, 82001642, 82101749]
  2. National Key Research and Development Program of China [2018YFC1002840, 2016YFC100600]
  3. Fundamental Research Funds for the Central Universities [2042021kf0082]
  4. Health Commission of Hubei Province scientific research project [WJ2021M158]

向作者/读者索取更多资源

The study found a significant decrease in the expression of EZH2 in villi tissue from RSA patients compared to healthy controls. Inhibition of EZH2 expression or function in trophoblasts promoted M1 macrophage polarization, potentially contributing to the pathogenesis of RSA. Additionally, EZH2 suppression affected the secretion of immune and inflammatory cytokines in trophoblasts.
Macrophages are known to be pivotal for ensuring the establishment of the immune tolerance microenvironment at the maternal-fetal interface. In particular, trophoblasts stay in close contact with decidual macrophages (DMs), which have been reported to play an active role in the modulation of the polarization of DMs. Thus, any dysfunction of trophoblasts might be associated with certain pregnancy-related complications, such as recurrent spontaneous abortion (RSA). Enhancer of zeste homolog 2 (EZH2) is an important epigenetic regulatory gene that has been previously shown to be related to immune regulation. The present study assessed the expression of EZH2 in villi tissue obtained from healthy controls and RSA patients. Trophoblasts conditioned medium was collected to incubate macrophages differentiated from the THP-1 cell line. The expression and function of EZH2 in trophoblasts were knocked down either by the use of siRNA or GSK126 as an inhibitor. Our results show a significant decrease in the expression of EZH2 in villi tissue from RSA patients as compared to healthy controls. Further, the inhibition of expression or function of EZH2 in trophoblasts promoted M1 macrophage polarization, which might be involved in the pathogenesis of RSA. Moreover, the suppression of EZH2 was found to affect the secretion of immune and inflammatory cytokines in trophoblasts. Altogether, these results indicated the importance of EZH2 in the regulation of immune functions of trophoblasts and thus highlighted its potential to be explored as a therapeutic target to prevent and treat pregnancy loss.

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