Kuwano Yoshihiro, Prazma Charlene M, Yazawa Norihito, Watanabe Rei, Ishiura Nobuko, Kumanogoh Atsushi, Okochi Hitoshi, Tamaki Kunihiko, Fujimoto Manabu, Tedder Thomas F
Department of Dermatology, Faculty of Medicine, University of Tokyo, Tokyo, Japan.
Int Immunol. 2007 Aug;19(8):977-92. doi: 10.1093/intimm/dxm067.
CD83 is a member of the Ig superfamily expressed primarily by mature dendritic cells (DCs). In mice, CD83 expression by thymic stromal cells regulates CD4(+) T cell development, with CD83(-/-) mice demonstrating dramatic reductions in both thymus and peripheral CD4(+) T cells. In this study, CD83 expression was also found to affect MHC class II antigen expression within the thymus and periphery. CD83 deficiency reduced cell-surface class II antigen expression by 25-50% on splenic B cells and DCs, thymic epithelial cells and peritoneal macrophages. Reduced class II expression was a stable and intrinsic property that resulted from increased internalization of class II from the surface of CD83(-/-) B cells. Otherwise, class II antigen transcription, intracellular expression, heterodimer structure, antigen processing and antigen presentation were normal. Reduced class II antigen expression was not the primary cause of the CD83(-/-) phenotype since thymocyte and peripheral T cell development was normal in class II(+/-) mice. Comparable blocks in CD4(+) thymocyte development were also observed in CD83(-/-) and CD83(-/-)class II(+/-) littermates. TCR and CD69 expression patterns in CD83(-/-) mice further suggested that double-positive thymocytes proceed through the class II-dependent stages of positive selection in the absence of CD83. These studies further emphasize a role for CD83 in lymphocyte development and immune regulation and reveal an unexpected role for CD83 expression in influencing cell-surface MHC class II turnover.
CD83是免疫球蛋白超家族的成员,主要由成熟树突状细胞(DC)表达。在小鼠中,胸腺基质细胞表达的CD83调节CD4(+) T细胞的发育,CD83基因敲除(-/-)小鼠的胸腺和外周CD4(+) T细胞显著减少。在本研究中,还发现CD83的表达会影响胸腺和外周的MHC II类抗原表达。CD83缺陷使脾脏B细胞、DC、胸腺上皮细胞和腹腔巨噬细胞表面的II类抗原表达降低了25%-50%。II类表达降低是一种稳定的内在特性,是由于CD83(-/-) B细胞表面II类分子内化增加所致。否则,II类抗原转录、细胞内表达、异二聚体结构、抗原加工和抗原呈递均正常。II类抗原表达降低不是CD83(-/-)表型的主要原因,因为II类(+/-)小鼠的胸腺细胞和外周T细胞发育正常。在CD83(-/-)和CD83(-/-)II类(+/-)同窝小鼠中也观察到CD4(+)胸腺细胞发育的类似阻滞。CD83(-/-)小鼠中的TCR和CD69表达模式进一步表明,在没有CD83的情况下,双阳性胸腺细胞会经历II类依赖性的阳性选择阶段。这些研究进一步强调了CD83在淋巴细胞发育和免疫调节中的作用,并揭示了CD83表达在影响细胞表面MHC II类分子周转方面的意外作用。