Triptolide inhibits tonsillar IgA production by upregulating FDC-SP in IgA nephropathy

雷公藤甲素 肾病 扁桃体 免疫学 腭扁桃体 医学 免疫球蛋白A 下调和上调 免疫组织化学 抗体 生物 内分泌学 免疫球蛋白G 基因 细胞凋亡 生物化学 糖尿病
作者
Huining Li,Xinxin Yang,Guo‐Dong Yao,Yanxiang Zhang,Yangyang Xu,Yan Cao,Xushu An,Haibo Li,Hui Chen,Jingshu Geng,Dawei Yuan,Xiaoming Jin,Hongxue Meng
出处
期刊:Histology and Histopathology [University of Murcia]
卷期号:35 (6): 599-608 被引量:6
标识
DOI:10.14670/hh-18-190
摘要

IgA nephropathy (IgAN) is primarily resulted of qualitative abnormality of IgA. The occurrence of IgAN is associated with affected tonsils which enhances the IgA production via IgA class switching and immuno-activation. Follicular dendritic cell-secreted protein (FDC-SP) was found to be a negative effect for IgA production in tonsil. The previous studies suggested that Triptolide might reduce IgA production by its immunosuppression role. Given this background, this study investigated the mechanisms underlying the role of Triptolide and FDC-SP in the generation of IgA and IgA class switching in tonsil of IgAN patients. Immunohistochemistry and reverse transcription-polymerase chain reaction revealed that the expression of FDC-SP was increased in the tonsils of IgAN patients with Triptolide treatment compared with those without treatment. Meanwhile, the expression of FDC-SP was negatively correlated with IgA inducing cytokines in the tonsils of IgAN patients treated with Triptolide, due to the significant decreased IgA-bearing cells. The expression of FDC-SP in tonsillar tissue was confirmed by double immunofluorescence. Importantly, Triptolide promoted FDC-SP secretion, and correlated negatively with decreased IgA production in isolated FDC-associated clusters, which had been isolated from patients without TW treatment previously. Our study demonstrated that Triptolide might have an impact on FDC-SP production and downregulation of IgA synthesis in the tonsils of IgAN patients, which could be a promising strategy for therapeutic intervention in IgAN patients.
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