Komaniwa Satoshi, Hayashi Hiroshi, Kawamoto Hiroshi, Sato Satoshi B, Ikawa Tomokatsu, Katsura Yoshimoto, Udaka Keiko
Department of Immunology, Kochi Medical School, Nankoku, Kochi, Japan.
Eur J Immunol. 2009 Jan;39(1):96-112. doi: 10.1002/eji.200838796.
Previous studies on the MHC class-specific differentiation of CD4(+)CD8(+) thymocytes into CD4(+) and CD8(+) T cells have focused on the role of coreceptor molecules. However, CD4 and CD8 T cells develop according to their MHC class specificities even in these mice lacking coreceptors. This study investigated the possibility that lineage is determined not only by coreceptors, but is also guided by the way how MHC molecules are presented. MHC class II molecules possess a highly conserved Cys in their transmembrane domain, which is palmitoylated and thereby associates with lipid rafts, whereas neither palmitoylation nor raft association was observed with MHC class I molecules. The generation of CD4 T cells was impaired and that of CD8 T cells was augmented when the rafts on the thymic epithelial cells were disrupted. This was due to the conversion of MHC class II-specific thymocytes from the CD4 lineage to CD8. The ability of I-A(d) molecule to associate with rafts was lost when its transmembrane Cys was replaced. The development of DO11.10 thymocytes recognizing this mutant I-A(dm) was converted from CD4 to CD8. These results suggest that the CD4 lineage commitment is directed by the raft-associated presentation of MHC class II molecules.
先前关于CD4(+)CD8(+)胸腺细胞向CD4(+)和CD8(+) T细胞进行MHC类别特异性分化的研究主要聚焦于共受体分子的作用。然而,即使在这些缺乏共受体的小鼠中,CD4和CD8 T细胞仍根据其MHC类别特异性进行发育。本研究调查了谱系不仅由共受体决定,还受MHC分子呈递方式引导的可能性。MHC II类分子在其跨膜结构域中具有一个高度保守的半胱氨酸,该半胱氨酸被棕榈酰化,从而与脂筏相关联,而MHC I类分子未观察到棕榈酰化或与脂筏的关联。当胸腺上皮细胞上的脂筏被破坏时,CD4 T细胞的生成受损,而CD8 T细胞的生成增加。这是由于MHC II类特异性胸腺细胞从CD4谱系转变为CD8谱系。当I-A(d)分子的跨膜半胱氨酸被取代时,其与脂筏关联的能力丧失。识别这种突变体I-A(dm)的DO11.10胸腺细胞的发育从CD4转变为CD8。这些结果表明,CD4谱系的定向由与脂筏相关的MHC II类分子呈递所引导。