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小GTP酶Rac2在CD8(+)树突状细胞中选择性地控制吞噬体碱化和抗原交叉呈递。

The small GTPase Rac2 controls phagosomal alkalinization and antigen crosspresentation selectively in CD8(+) dendritic cells.

作者信息

Savina Ariel, Peres Audrey, Cebrian Ignacio, Carmo Nuno, Moita Catarina, Hacohen Nir, Moita Luis F, Amigorena Sebastian

机构信息

Institut Curie, INSERM U653, Immunité et Cancer, 26 rue d'Ulm, 75248 Paris, Cedex 05, France.

出版信息

Immunity. 2009 Apr 17;30(4):544-55. doi: 10.1016/j.immuni.2009.01.013. Epub 2009 Mar 26.

Abstract

A unique subpopulation of spleen dendritic cells (DCs) that express the CD8 surface marker efficiently present phagocytosed antigens to CD8(+) T lymphocytes in a process called "crosspresentation," which initiates cytotoxic immune responses. We now show that the small GTPase Rac2 plays a critical role in antigen crosspresentation selectively in this DC subpopulation. In CD8(+) DCs, Rac2 determines the subcellular assembly of the NADPH oxidase complex (NOX2) to phagosomes, whereas in CD8(-) DCs, Rac1 mediates the assembly of NOX2 at the plasma membrane. In the absence of Rac2, the production of reactive oxygen species (ROS) in DC-phagosomes was abolished, the phagosomal pH dropped, and the efficiency of antigen crosspresentation was reduced. We conclude that the activity of Rac1 and 2 control crosspresentation in DC subpopulations through the regulation of phagosomal oxidation and pH.

摘要

脾脏树突状细胞(DC)中有一个独特的亚群,其表达CD8表面标志物,能在一个名为“交叉呈递”的过程中有效地将吞噬的抗原呈递给CD8(+) T淋巴细胞,从而启动细胞毒性免疫反应。我们现在发现,小GTP酶Rac2在这一DC亚群的抗原交叉呈递中选择性地发挥关键作用。在CD8(+) DC中,Rac2决定了NADPH氧化酶复合物(NOX2)向吞噬体的亚细胞组装,而在CD8(-) DC中,Rac1介导NOX2在质膜上的组装。在没有Rac2的情况下,DC吞噬体中的活性氧(ROS)生成被消除,吞噬体pH值下降,抗原交叉呈递效率降低。我们得出结论,Rac1和Rac2的活性通过调节吞噬体氧化和pH值来控制DC亚群中的交叉呈递。

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