相扑蛋白
胞苷脱氨酶
体细胞突变
生发中心
活化诱导(胞苷)脱氨酶
免疫球蛋白类转换
分子生物学
细胞生物学
乘客5人
生物
B细胞
化学
遗传学
泛素
基因
生物化学
抗体
作者
Jingjing Qi,Yan Luo,Jiping Sun,Chuanxin Huang,Bing Su,Jinke Cheng,Lei Shen
标识
DOI:10.1073/pnas.2314619121
摘要
Humoral immunity depends on the germinal center (GC) reaction where B cells are tightly controlled for class-switch recombination and somatic hypermutation and finally generated into plasma and memory B cells. However, how protein SUMOylation regulates the process of the GC reaction remains largely unknown. Here, we show that the expression of SUMO-specific protease 1 (SENP1) is up-regulated in GC B cells. Selective ablation of SENP1 in GC B cells results in impaired GC dark and light zone organization and reduced IgG1-switched GC B cells, leading to diminished production of class-switched antibodies with high-affinity in response to a TD antigen challenge. Mechanistically, SENP1 directly binds to Paired box protein 5 (PAX5) to mediate PAX5 deSUMOylation, sustaining PAX5 protein stability to promote the transcription of activation-induced cytidine deaminase. In summary, our study uncovers SUMOylation as an important posttranslational mechanism regulating GC B cell response.
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