期刊
ADVANCED SCIENCE
卷 -, 期 -, 页码 -出版社
WILEY
DOI: 10.1002/advs.202305175
关键词
aging; cell death; developmental trajectory; immune cells; intercellular communication; macrophage; ovary; pyroptosis; senescence; single-cell RNA sequencing
The activation of pyroptotic macrophages in human ovaries increases with age, leading to changes in the ovarian immune microenvironment and accelerated reproductive decline. This discovery provides important insights into the aging process of the ovaries and offers potential strategies for delaying senescence and promoting reproductive health.
Female fecundity declines in a nonlinear manner with age during the reproductive years, even as ovulatory cycles continue, which reduces female fertility, disrupts metabolic homeostasis, and eventually induces various chronic diseases. Despite this, the aging-related cellular and molecular changes in human ovaries that occur during these reproductive years have not been elucidated. Here, single-cell RNA sequencing (scRNA-seq) of human ovaries is performed from different childbearing ages and reveals that the activation of the pyroptosis pathway increased with age, mainly in macrophages. The enrichment of pyroptotic macrophages leads to a switch from a tissue-resident macrophage (TRM)-involve immunoregulatory microenvironment in young ovaries to a pyroptotic monocyte-derived macrophage (MDM)-involved proinflammatory microenvironment in middle-aged ovaries. This remolded ovarian immuno-microenvironment further promotes stromal cell senescence and accelerated reproductive decline. This hypothesis is validated in a series of cell and animal experiments using GSDMD-KO mice. In conclusion, the work expands the current understanding of the ovarian aging process by illustrating a pyroptotic macrophage-involved immune mechanism, which has important implications for the development of novel strategies to delay senescence and promote reproductive health. ScRNA-seq analysis of human ovaries identified age-related changes in cellular interactomes during reproductive years.The immune regulatory mechanisms of ovarian aging are underscored by emphasizing the central role of pyroptotic macrophages in accelerating collagen deposition and stromal cell senescence in elder ovaries, which eventually lead to ovarian function decline.image
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