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复发性流产患者外周B细胞免疫调节能力的诱导性受损。

Impaired inducibility of immune regulatory capacity of peripheral B cells of patients with recurrent pregnancy loss.

作者信息

Ma Fei, Feng Xiaoyang, Feng Shiyu, Liu Jin, Li Jia, Mo Lihua, Xu Lingzhi, Liu Yulei, Wu Jiaman, Yang Pingchang, Ning Yan

机构信息

Department of Chinese Traditional Medicine, Affiliated Shenzhen Maternity & Child Healthcare Hospital, Southern Medical University, Shenzhen, China.

School of Traditional Chinese Medicine, Southern Medical University, Guangzhou, China.

出版信息

Immunol Res. 2024 Dec;72(6):1502-1514. doi: 10.1007/s12026-024-09549-7. Epub 2024 Nov 4.

Abstract

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.

摘要

复发性流产(RPL)的发病机制尚不清楚。RPL可能与免疫耐受的破坏有关。本研究的目的是表征RPL患者外周幼稚B细胞免疫调节能力的可诱导性。在本研究中,采集了RPL患者的血样。通过流式细胞术细胞分选分离出B220 B细胞。使用RNA测序(RNAseq)分析B细胞的基因谱。结果显示,RPL患者的外周B220 B细胞中IL10表达较低,内质网应激加剧。RPL患者外周B220 B细胞中IL10表达的诱导受损。在RPL B细胞中检测到c-Maf诱导蛋白(CMIP)的高泛素化。暴露于毒胡萝卜素(一种内质网应激激动剂)可降低B细胞中CMIP的量。内质网应激对降低B细胞中CMIP量的影响由组蛋白H2B E3泛素连接酶环指蛋白20(RNF20)介导。抑制RNF20或内质网应激可恢复RPL患者B220 B细胞免疫调节功能的可诱导性。总之,RPL患者的外周B细胞显示出免疫调节能力受损,其中内质网应激加剧起着关键作用。内质网应激的调节或RNF20的抑制可恢复B细胞中的免疫调节能力。

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