淋巴
细胞生物学
启动(农业)
运动性
免疫学
T细胞
抗原提呈细胞
T淋巴细胞
细胞因子
化学
树突状细胞
淋巴结
生物
免疫系统
抗原
医学
病理
发芽
植物
作者
Thorsten R. Mempel,Sarah E. Henrickson,Ulrich H. von Andrian
出处
期刊:Nature
[Nature Portfolio]
日期:2004-01-01
卷期号:427 (6970): 154-159
被引量:1671
摘要
Primary T-cell responses in lymph nodes (LNs) require contact-dependent information exchange between T cells and dendritic cells (DCs). Because lymphocytes continually enter and leave normal LNs, the resident lymphocyte pool is composed of non-synchronized cells with different dwell times that display heterogeneous behaviour in mouse LNs in vitro. Here we employ two-photon microscopy in vivo to study antigen-presenting DCs and naive T cells whose dwell time in LNs was synchronized. During the first 8 h after entering from the blood, T cells underwent multiple short encounters with DCs, progressively decreased their motility, and upregulated activation markers. During the subsequent 12 h T cells formed long-lasting stable conjugates with DCs and began to secrete interleukin-2 and interferon-gamma. On the second day, coinciding with the onset of proliferation, T cells resumed their rapid migration and short DC contacts. Thus, T-cell priming by DCs occurs in three successive stages: transient serial encounters during the first activation phase are followed by a second phase of stable contacts culminating in cytokine production, which makes a transition into a third phase of high motility and rapid proliferation.
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