Vivar Omar I, Magalhaes Joao G, Amigorena Sebastian
INSERM U932 and Institut Curie, Centre de recherche, 26 Rue d'Ulm, 75005, Paris, France.
Methods Mol Biol. 2016;1423:183-8. doi: 10.1007/978-1-4939-3606-9_13.
The presentation of exogenous antigens on MHC class I molecules, known as cross-presentation, is a key function of dendritic cells (DCs). Cross-presentation via the cytosolic pathway involves antigen export from endocytic compartments to the cytosol. We have recently developed a cytofluorimetry-based assay to examine the kinetics and the efficiency of antigen export to the cytosol in DC populations. In this assay, DCs are loaded with a FRET-sensitive cytosolic substrate of β-lactamase, CCF4. Following uptake of β-lactamase by the DCs, the enzyme undergoes export to the cytosol leading to cleavage of the FRET dye. This cleavage and switch of fluorescence are analyzed by flow cytometry, allowing a quantitative measurement of this event.
外源性抗原在MHC I类分子上的呈递,即交叉呈递,是树突状细胞(DC)的一项关键功能。通过胞质途径的交叉呈递涉及抗原从内吞区室转运至胞质溶胶。我们最近开发了一种基于细胞荧光测定法的检测方法,以研究DC群体中抗原转运至胞质溶胶的动力学和效率。在该检测方法中,DC被加载一种对FRET敏感的β-内酰胺酶胞质底物CCF4。DC摄取β-内酰胺酶后,该酶会转运至胞质溶胶,导致FRET染料裂解。通过流式细胞术分析这种裂解和荧光转换,从而对该事件进行定量测量。