Fei Ma, Xiaoyang Feng, Shiyu Feng, Jin Liu, Jia Li, Lihua Mo, Lingzhi Xu, Yulei Liu, Jiaman Wu, Pingchang Yang, Yan Ning
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引用次数: 0
摘要
复发性妊娠失败(RPL)的发病机制尚不清楚。RPL可能与免疫耐受的破坏有关。本研究的目的是鉴定 RPL 患者外周幼稚 B 细胞免疫调节能力的诱导性。本研究采集了 RPL 患者的血液样本。通过流式细胞术细胞分拣分离出 B220+ B 细胞。利用 RNA 测序(RNAseq)分析了 B 细胞的基因图谱。结果显示,RPL 患者外周 B220+ B 细胞的 IL10 表达较低,ER 应激加剧。RPL患者外周B220+ B细胞中IL10的诱导表达受损。在RPL B细胞中检测到了c-Maf诱导蛋白(CMIP)的高泛素化。暴露于硫司加精(一种ER应激激动剂)可减少B细胞中CMIP的数量。ER应激对减少B细胞中CMIP数量的影响是由组蛋白H2B E3泛素连接酶环指蛋白20(RNF20)介导的。抑制 RNF20 或 ER 应激可恢复 RPL 患者 B220+ B 细胞免疫调节功能的诱导性。总之,RPL 患者的外周 B 细胞显示出免疫调节能力受损,ER 应激的加剧在其中发挥了关键作用。调节ER应激或抑制RNF20可恢复B细胞的免疫调节能力。
Impaired inducibility of immune regulatory capacity of peripheral B cells of patients with recurrent pregnancy loss.
The pathogenesis of recurrent pregnancy loss (RPL) is unclear. RPL may have an association with disruption of immune tolerance. The aim of this study is to characterize the inducibility of immune regulatory ability in peripheral naïve B cells of patients with RPL. In this study, blood samples were taken from patients with RPL. B220+ B cells were isolated by flow cytometry cell sorting. The gene profile of B cells was analyzed using RNA sequencing (RNAseq). The results showed that peripheral B220+ B cells of RPL patients had lower expression of IL10 and exacerbated ER stress. The induction of IL10 expression in peripheral B220+ B cells of RPL patients were impaired. High ubiquitination of c-Maf inducing protein (CMIP) was detected in RPL B cells. Exposure to thapsigargin (an ER stress agonist) decreased the amount of CMIP in B cells. The effects of ER stress on reducing CMIP quantity in B cells were mediated by the histone H2B E3 ubiquitin ligase ring finger protein 20 (RNF20). Inhibition of RNF20 or ER stress restored the inducibility of immune regulatory functions of B220+ B cells of RPL patients. In summary, peripheral B cells in patients with RPL show impaired immune regulation capacity, in which exacerbated ER stress plays a crucial role. Regulation of ER stress or inhibition of RNF20 can restore the immune regulatory capacity in the B cells.