The effect of intracellular trafficking of CD1d on the formation of TCR repertoire of NKT cells

被引:7
|
作者
Shin, Jung Hoon [1 ]
Park, Se-Ho [1 ]
机构
[1] Korea Univ, Dept Life Sci, Seoul 136701, South Korea
基金
新加坡国家研究基金会;
关键词
Antigen presentation; CD1d; Endosome; Endolysosomal compartment; Glycolipid; Lysosome; NKT cells; KILLER T-CELLS; C-GLYCOSIDE ANALOG; LIGAND ALPHA-GALACTOSYLCERAMIDE; TRIGLYCERIDE TRANSFER PROTEIN; CLASS-II MOLECULES; ANTIGEN PRESENTATION; MULTIPLE DEFECTS; SELF-ANTIGENS; LIPID ANTIGEN; RECOGNITION;
D O I
10.5483/BMBRep.2014.47.5.077
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
CD1 molecules belong to non-polymorphic MHC class I-like proteins and present lipid antigens to T cells. Five different CD1 genes (CD1a-e) have been identified and classified into two groups. Group 1 include CD1a-c and present pathogenic lipid antigens to alpha beta T cells reminiscence of peptide antigen presentation by MHC-I molecules. CD1d is the only member of Group 2 and presents foreign and self lipid antigens to a specialized subset of alpha beta T cells, NKT cells. NKT cells are involved in diverse immune responses through prompt and massive production of cytokines. CD1d-dependent NKT cells are categorized upon the usage of their T cell receptors. A major subtype of NKT cells (type I) is invariant NKT cells which utilize invariant V alpha 14-J alpha 18 TCR alpha chain in mouse. The remaining NKT cells (type II) utilize diverse TCR alpha chains. Engineered CD1d molecules with modified intracellular trafficking produce either type I or type II NKT cell-defects suggesting the lipid antigens for each subtypes of NKT cells are processed/generated in different intracellular compartments. Since the usage of TCR by a T cell is the result of antigen-driven selection, the intracellular metabolic pathways of lipid antigen are a key in forming the functional NKT cell repertoire.
引用
收藏
页码:241 / 248
页数:8
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