期刊
TRANSLATIONAL RESEARCH
卷 259, 期 -, 页码 46-61出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.trsl.2023.04.004
关键词
sterile intra-amniotic inflammation; inflammasome; prematurity; fetus; neonate; preterm birth; parturition
Preterm birth is a major cause of neonatal morbidity and mortality worldwide. Sterile intra-amniotic inflammation, triggered by alarmins, is a common condition associated with preterm labor. The NLRP3 inflammasome has been implicated in this process, but its mechanisms are not fully understood. By studying Nlrp3-/- mice, researchers found that NLRP3 deficiency prevents preterm birth and neonatal mortality by inhibiting premature labor activation and reducing inflammation. Furthermore, both maternal and fetal Nlrp3 signaling contribute to alarmin-induced preterm birth. These findings highlight the importance of targeting NLRP3 signaling to prevent adverse perinatal outcomes.
Preterm birth remains the leading cause of neonatal morbidity and mortality worldwide. A substantial number of spontaneous preterm births occur in the context of sterile intra-amniotic inflammation, a condition that has been mechanistically proven to be triggered by alarmins. However, sterile intra-amniotic inflammation still lacks treatment. The NLRP3 inflammasome has been implicated in sterile intra-amniotic inflammation; yet, its underlying mechanisms, as well as the maternal and fetal contributions to this signaling pathway, are unclear. Herein, by utilizing a translational and clinically relevant model of alarmin-induced preterm labor and birth in Nlrp3-/- mice, we investigated the role of NLRP3 signaling by using imaging and molecular biology approaches. Nlrp3 deficiency abrogated preterm birth and the resulting neonatal mortality induced by the alarmin S100B by impeding the premature activation of the common pathway of labor as well as by dampening intra-amniotic and fetal inflammation. Moreover, Nlrp3 deficiency altered leukocyte infiltration and functionality in the uterus and decidua. Last, embryo transfer revealed that maternal and fetal Nlrp3 signaling contribute to alarmin-induced preterm birth and neonatal mortality, further strengthening the concept that both individuals participate in the complex process of preterm parturition. These findings provide novel insights into sterile intra-amniotic inflammation, a common etiology of preterm labor and birth, suggesting that the adverse perinatal outcomes resulting from prematurity can be prevented by targeting NLRP3 signaling.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据