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使用基于细胞荧光测定法测量树突状细胞向细胞质的输出。

Measurement of Export to the Cytosol in Dendritic Cells Using a Cytofluorimetry-Based Assay.

作者信息

Vivar Omar I, Magalhaes Joao G, Amigorena Sebastian

机构信息

INSERM U932 and Institut Curie, Centre de recherche, 26 Rue d'Ulm, 75005, Paris, France.

出版信息

Methods Mol Biol. 2016;1423:183-8. doi: 10.1007/978-1-4939-3606-9_13.

Abstract

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.

摘要

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。

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