4.6 Article

Features of peritoneal dendritic cells in the development of endometriosis

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BMC
DOI: 10.1186/s12958-023-01058-w

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Endometriosis; Peritoneal dendritic cells; DCs maturation; Immature DCs; Mature DCs

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This study found that there is an increased number of dendritic cells (DCs) in the peritoneal cavity of endometriosis patients, with a decreased proportion of mature DCs and an increased proportion of immature DCs. Similar results were observed in a mouse model of endometriosis. These findings are important for further understanding the pathogenesis of endometriosis and providing new insights into medical treatment.
BackgroundEmerging evidence of immunological dysfunction have been described in endometriosis. Dendritic cells (DCs), one of the main antigen-presenting cells, are specialized in the initiation and modulation of the adaptive immune response. Emerging studies demonstrated both endometrial and circulating differences in DCs populations in women with endometriosis. However, the role and mechanism of peritoneal DCs in endometriosis is still unclear. The present study was undertaken to explore the features of peritoneal DCs in the pathogenesis of endometriosis. This study is beneficial to further clarify the cause of endometriosis and provide a new insight into the medical treatment for endometriosis.MethodsThe study included 12 women with endometriosis and 11 women without endometriosis. The C57BL6 mouse model of endometriosis was established by intraperitoneal injection of endometrial segments. The peritoneal DCs of endometriosis patients and mouse models were analyzed by fluorescence associated cell sorting (FACS) examination.ResultsIncreased cell density of peritoneal DCs were observed in endometriosis patients. Moreover, the proportion of mature DCs (mDCs, CD80(high)CD1a(low) cells) in the peritoneal DCs was lower whereas the proportion of immature DCs (iDCs, CD80(low)CD1a(high) cells) was increased in endometriosis patients. Similarly, the cell density of peritoneal DCs in murine models increased immediately after the injection of endometrial tissues and reached the highest level at 14 days. In addition, the proportion of mDCs (CD11c(high)CD80(high) cells) in the peritoneal DCs decreased immediately after the injection of endometrial tissues and then increased with the time until 42 days, but still lower than the control group. In contrast, the proportion of iDCs (CD11c(high)CD80(low) cells) in the peritoneal DCs showed the opposite dynamic changes. However, after treated with LPS, the mDCs proportion was significantly increased, leading to lower volume and weight of the endometriosis lesions.ConclusionsIncreased level of peritoneal DCs facilitated the pathogenesis of endometriosis lesions, especially in the early stage of the disease. Furthermore, peritoneal DCs maturation played an important role in the development of endometriosis.

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