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The histone H2B ubiquitination regulator Wac is essential for plasma cell differentiation
被引:2
|作者:
Li, Yuxing
[1
]
Ruan, Gui-Xin
[2
]
Chen, Wenjing
[1
]
Huang, Hengjun
[1
]
Zhang, Rui
[1
]
Wang, Jing
[1
]
Ouyang, Yu
[1
]
Zhu, Zhijian
[1
]
Meng, Limin
[1
]
Wang, Ruisi
[1
]
Huo, Jianxin
[3
]
Xu, Shengli
[3
,4
]
Ou, Xijun
[1
]
机构:
[1] Southern Univ Sci & Technol, Sch Life Sci, Shenzhen 518055, Peoples R China
[2] Taizhou Univ, Med Sch, Taizhou, Zhejiang, Peoples R China
[3] Agcy Sci Technol & Res, Singapore Immunol Network, Singapore 138648, Singapore
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Physiol, Singapore, Singapore
基金:
中国国家自然科学基金;
关键词:
antibody response;
B cell;
H2B ubiquitination;
plasma cell;
Wac;
B-CELL;
MEMORY B;
EXPRESSION;
PROTEIN;
D O I:
10.1002/1873-3468.14633
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Naive B cells become activated and differentiate into antibody-secreting plasma cells (PCs) when encountering antigens. Here, we reveal that the WW domain-containing adapter protein with coiled-coil (Wac), which is important for histone H2B ubiquitination (ubH2B), is essential for PC differentiation. We demonstrate that B cell-specific Wac knockout mice have severely compromised T cell-dependent and -independent antibody responses. PC differentiation is drastically compromised despite undisturbed germinal center B cell response in the mutant mice. We also observe a significant reduction in global ubH2B in Wac-deficient B cells, which is correlated with downregulated expression of some genes critical for cell metabolism. Thus, our findings demonstrate an essential role of Wac-mediated ubH2B in PC differentiation and shed light on the epigenetic mechanisms underlying this process.
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页码:1748 / 1760
页数:13
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