HIF1A-induced heme oxygenase 1 promotes the survival of decidual stromal cells against excess heme-mediated oxidative stress

• DOI: 10.1530/rep-21-0314
• Publication Date: 2021-12-07T13:54:38Z
• Authors: Hui-Hui Shen; Cheng-Jie Wang; Xin-Yan Zhang; Yan-Ran Sheng; Shao-Liang Yang; Zi-Meng Zheng; Jia-Lu Shi; Xue-Min Qiu; Feng Xie; Ming-Qing Li
• Keywords: Cell Survival; NF-E2-Related Factor 2; Apoptosis; Heme; Hydrogen Peroxide; Hypoxia-Inducible Factor 1, alpha Subunit; Oxidative Stress; 03 medical and health sciences; 0302 clinical medicine; Humans; Stromal Cells; Reactive Oxygen Species; Heme Oxygenase-1

Heme oxygenase 1 (HO-1, encoded by the HMOX1 gene) is the rate-limiting enzyme that catalyzes heme degradation, and it has been reported to exert antioxidative effects. Recently, decidualization has been reported to confer resistance to environmental stress signals, protecting against oxidative stress. However, the effects and regulatory mechanism of HO-1 in decidual stromal cells (DSCs) during early pregnancy remain unknown. Here, we verified that the levels of HO-1 and heme in DSCs are increased compared with those in endometrial stromal cells. Additionally, the upregulation of HIF1A expression led to increased HMOX1 expression in DSCs possibly via nuclear factor erythroid 2-related factor (encoded by the NFE2L2 gene). However, addition of the competitive HO-1 inhibitor zinc protoporphyrin IX resulted in an increase in HIF1A expression. Hydrogen peroxide (H2O2) induced the production of reactive oxygen species (ROS), decreased the cell viability of DSCs in vitro, and upregulated the level of heme. As an HO-1 inducer, cobalt protoporphyrin IX decreased ROS production and significantly reversed the inhibitory effect of H2O2 on cell viability. More importantly, patients with unexplained spontaneous abortion had low levels of HO-1 that were insufficient to protect against oxidative stress. This study suggests that the upregulation of HO-1 expression via HIF1A protects DSCs against excessive heme-mediated oxidative stress. Furthermore, the excessive oxidative stress injury and impaired viability of DSCs associated with decreased HO-1 expression should be associated with the occurrence and/or development of spontaneous abortion.