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CD8α⁺树突状细胞通过一个涉及CD8α、DEC-205和CD24上调的成熟过程,从CD8α⁻树突状细胞亚群分化而来。

CD8alpha+ dendritic cells originate from the CD8alpha- dendritic cell subset by a maturation process involving CD8alpha, DEC-205, and CD24 up-regulation.

作者信息

Martinez del Hoyo Gloria, Martín Pilar, Arias Cristina Fernández, Marín Alvaro Rodríguez, Ardavín Carlos

机构信息

Department of Cell Biology, Faculty of Biology, Complutense University, 28040 Madrid, Spain.

出版信息

Blood. 2002 Feb 1;99(3):999-1004. doi: 10.1182/blood.v99.3.999.

Abstract

CD8alpha+ and CD8alpha- dendritic cells (DCs) have been considered as independent DC subpopulations both ontogenetically and functionally during recent years. However, it has been demonstrated that both DC subsets can be generated from a single precursor population, supporting the concept that they do not represent separate DC lineages. By using highly purified splenic CD8alpha- DCs, which were injected intravenously and traced by means of an Ly5.1/Ly5.2 transfer system, this study shows that CD8alpha- DCs acquired the phenotypic characteristics of CD8alpha+ DCs, by a differentiation process involving CD8alpha, DEC-205, and CD24 up-regulation, paralleled by the down-regulation of CD11b, F4/80, and CD4. These data demonstrate that CD8alpha+ DCs derive from CD8alpha- DCs, and strongly support that CD8alpha- and CD8alpha+ DCs represent different maturation or differentiation stages of the same DC population. Therefore, CD8alpha+ DCs would represent the last stage of DC differentiation, playing an essential role in the induction of T-cell responses, due to their antigen-presenting potential, cross-priming ability, and capacity to secrete large amounts of key cytokines such as interferon gamma and interleukin-12.

摘要

近年来,CD8α⁺和CD8α⁻树突状细胞(DCs)在个体发生和功能上都被视为独立的DC亚群。然而,已经证明这两种DC亚群都可以从单个前体细胞群体产生,这支持了它们不代表独立DC谱系的概念。通过使用经静脉注射并借助Ly5.1/Ly5.2转移系统追踪的高度纯化的脾CD8α⁻DCs,本研究表明,CD8α⁻DCs通过涉及CD8α、DEC-205和CD24上调以及CD11b、F4/80和CD4下调的分化过程,获得了CD8α⁺DCs的表型特征。这些数据表明CD8α⁺DCs来源于CD8α⁻DCs,并有力地支持CD8α⁻和CD8α⁺DCs代表同一DC群体的不同成熟或分化阶段。因此,CD8α⁺DCs可能代表DC分化的最后阶段,由于其抗原呈递潜能、交叉启动能力以及分泌大量关键细胞因子(如干扰素γ和白细胞介素-12)的能力,在诱导T细胞反应中发挥重要作用。

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