Core Fucosylation Regulates the Function of Pre-BCR, BCR and IgG in Humoral Immunity

被引:25
作者
Sun, Yuhan [1 ,2 ]
Li, Xueying [3 ]
Wang, Tiantong [1 ]
Li, Wenzhe [1 ]
机构
[1] Dalian Med Univ, Coll Basic Med Sci, Dalian, Peoples R China
[2] Tohoku Pharmaceut Univ, Inst Mol Biomembrane & Glycobiol, Div Regulatory Glycobiol, Sendai, Japan
[3] Osaka Univ, Res Inst Microbial Dis, World Premier Int Immunol Frontier Res Ctr, Suita, Japan
关键词
core fucosylation; pre-B cell; BCR; IgG; humoral immune response; B-CELL RECEPTOR; HIGH-AFFINITY; T-CELLS; ALPHA-1,6-FUCOSYL-TRANSFERASE-DEFICIENT MICE; CRYSTAL-STRUCTURE; N-GLYCOSYLATION; LIPID RAFTS; FUCOSE; ACTIVATION; GLYCANS;
D O I
10.3389/fimmu.2022.844427
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Most of the membrane molecules involved in immune response are glycosylated. N-glycans linked to asparagine (Asn) of immune molecules contribute to the protein conformation, surface expression, stability, and antigenicity. Core fucosylation catalyzed by core fucosyltransferase (FUT8) is the most common post-translational modification. Core fucosylation is essential for evoking a proper immune response, which this review aims to communicate. First, FUT8 deficiency suppressed the interaction between mu HC and lambda 5 during pre-BCR assembly is given. Second, we described the effects of core fucosylation in B cell signal transduction via BCR. Third, we investigated the role of core fucosylation in the interaction between helper T (T-H) cells and B cells. Finally, we showed the role of FUT8 on the biological function of IgG. In this review, we discussed recent insights into the sites where core fucosylation is critical for humoral immune responses.
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页数:12
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