Karadimitris A, Gadola S, Altamirano M, Brown D, Woolfson A, Klenerman P, Chen J L, Koezuka Y, Roberts I A, Price D A, Dusheiko G, Milstein C, Fersht A, Luzzatto L, Cerundolo V
Nuffield Department of Medicine, Institute of Molecular Medicine, Oxford OX3 9DS, United Kingdom.
Proc Natl Acad Sci U S A. 2001 Mar 13;98(6):3294-8. doi: 10.1073/pnas.051604498.
CD1 molecules are specialized in presenting lipids to T lymphocytes, but identification and isolation of CD1-restricted lipid specific T cells has been hampered by the lack of reliable and sensitive techniques. We here report the construction of CD1d-glycolipid tetramers from fully denatured human CD1d molecules by using the technique of oxidative refolding chromatography. We demonstrate that chaperone- and foldase-assisted refolding of denatured CD1d molecules and beta(2)-microglobulin in the presence of synthetic lipids is a rapid method for the generation of functional and specific CD1d tetramers, which unlike previously published protocols ensures isolation of CD1d tetramers loaded with a single lipid species. The use of human CD1d-alpha-galactosylceramide tetramers for ex vivo staining of peripheral blood lymphocytes and intrahepatic T cells from patients with viral liver cirrhosis allowed for the first time simultaneous analysis of frequency and specificity of natural killer T cells in human clinical samples. Application of this protocol to other members of the CD1 family will provide powerful tools to investigate lipid-specific T cell immune responses in health and in disease.
CD1分子专门负责将脂质呈递给T淋巴细胞,但由于缺乏可靠且灵敏的技术,对CD1限制性脂质特异性T细胞的鉴定和分离一直受到阻碍。我们在此报告通过氧化重折叠色谱技术从完全变性的人CD1d分子构建CD1d-糖脂四聚体。我们证明,在合成脂质存在的情况下,伴侣蛋白和折叠酶辅助变性的CD1d分子及β2微球蛋白重折叠是生成功能性和特异性CD1d四聚体的快速方法,与先前发表的方案不同,该方法可确保分离出负载单一脂质种类的CD1d四聚体。使用人CD1d-α-半乳糖神经酰胺四聚体对病毒性肝硬化患者的外周血淋巴细胞和肝内T细胞进行体外染色,首次实现了对人类临床样本中自然杀伤T细胞频率和特异性的同时分析。将该方案应用于CD1家族的其他成员将为研究健康和疾病状态下脂质特异性T细胞免疫反应提供强大工具。