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Core Fucosylation Regulates the Function of Pre-BCR, BCR and IgG in Humoral Immunity.
Sun, Yuhan; Li, Xueying; Wang, Tiantong; Li, Wenzhe.
Afiliação
  • Sun Y; College of Basic Medical Science, Dalian Medical University, Dalian, China.
  • Li X; Division of Regulatory Glycobiology, Institute of Molecular Biomembrane and Glycobiology, Tohoku Pharmaceutical University, Sendai, Japan.
  • Wang T; Research Institute for Microbial Diseases and World Premier International Immunology Frontier Research Center, Osaka University, Suita, Japan.
  • Li W; College of Basic Medical Science, Dalian Medical University, Dalian, China.
Front Immunol ; 13: 844427, 2022.
Article em En | MEDLINE | ID: mdl-35401499
ABSTRACT
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 µHC and λ5 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 (TH) 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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunidade Humoral / Fucose Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunidade Humoral / Fucose Idioma: En Ano de publicação: 2022 Tipo de documento: Article