Endoplasmic reticulum stress response and the regulation of endometrial interferon-beta production

Abstract

To gain an understanding of the potential role of endoplasmic reticulum (ER) stress in the endometrial compartment during early pregnancy, a highly understudied area. This study examined the regulation of interferon-β (IFNβ) in response to ER stress in human decidualized and nondecidualized endometrial cells (human endometrial stromal cells [HESCs]) invitro. Invivo, we examined ER stress and the IFNβ levels locally in the mouse endometrium before and after implantation at embryonic day (E)1, E3, and E6. The study was performed in a reproductive sciences laboratory for Human Growth and Development. None. None. Quantitative polymerase chain reaction, Western blotting, and immunohistochemical analysis allowed us to test the action of endogenous ER stress activation in the endometrial compartment likely triggered by implantation and its ability to increase the endometrial IFNβ levels. Invitro, we observed a significant difference in the IFNβ levels in HESCs, in response to ER stress activation, where decidualized HESCs exhibited a threefold increase in the IFNβ levels compared with nondecidualized HESCs. Apoptotic caspase-3 activation was also isolated to the decidualized cells as a result of ER stress-dependent suppression of nuclear factor-kappa beta-regulated antiapoptotic factors, XIAP and MCL-1. Invivo, mouse endometrial IFNβ was present in F4/80-positive macrophages at all time points examined. After implantation (E6), the mouse luminal epithelial cells robustly coexpressed both IFNβ and the ER stress marker immunoglobulin heavy chain binding protein (BiP). These analyses demonstrate that both invivo and invitro, differentiated and decidualized endometrial cells undergoing ER stress have the capacity to produce increased IFNβ levels; therefore, ER stress activation in the endometrial compartment may play a vital role in promoting successful implantation events.