17β-Estradiol promotes LC3B-associated phagocytosis in trained immunity of female mice against sepsis

Sepsis is a common serious clinical infectious disease accompanied by more severe injuries and higher mortality rates in men than women. The much higher level of 17 beta-estradiol (E-2) in female is one of the significant reasons for better sepsis resistance ability. Trained immunity is a novel way to fight against infection by improving innate immunity. However, whether beta-glucan-induced trained immunity can promote macrophage phagocytosis to clear infections in early sepsis has not been clarified. And whether E-2 involved in this process needs further investigation. Symptoms among male, female and ovariectomized (OVX) C57BL/6 mice in early sepsis were detected. The effect of trained immunity on macrophage LC3B-associated phagocytosis (LAP) and the mechanism of E-2 functioned in this process have also been explored. We demonstrated compared with male mice, female has significantly more mild symptoms and more reactive oxygen species (ROS) production and stronger NADPH oxidase 2 (NOX2) expression in the macrophage of major organs. In contrary, these characteristics are disappeared in OVX mice. Furthermore, in macrophage cell lines and primary bone marrow- derived macrophages (BMDMs), beta-glucan-induced trained immunity can increase ROS production by activating NOX2 to promote macrophage LAP. E-2 can up-regulate RUBICON through estrogen receptor a (ER alpha) to further facilitate macrophage LAP. These results indicated that trained immunity can improve sepsis resistance ability by stimulating macrophage LAP. E-2 can boost ROS production and RUBICON expression to further promote macrophage LAP, which can provide a new perspective to recognize the mechanism of trained immunity in gender differences when responding to sepsis.

Automated summary

Females show better resistance to sepsis with milder symptoms, higher ROS production, and stronger NOX2 expression in macrophages compared to males and OVX mice. Beta-glucan-induced trained immunity can enhance macrophage LAP by increasing ROS production through NOX2 activation. E-2 up-regulates RUBICON via ERα to further facilitate macrophage LAP, providing a new perspective on the mechanism of trained immunity in gender differences during sepsis response.