Department of Hematology, Oncology, Immunology, Rheumatology and Pulmonology, University Hospital, University of Tübingen, Tübingen, Germany.
Front Immunol. 2018 Mar 2;9:375. doi: 10.3389/fimmu.2018.00375. eCollection 2018.
T-cell development is coupled with a highly ordered migratory pattern. Lymphoid progenitors must follow a precise journey; starting from the hematopoietic tissue, they move toward the thymus and then migrate into and out of distinct thymic microenvironments, where they receive signals and cues required for their differentiation into naïve T-cells. Knowing where, when, and how these cells make directional "decisions" is key to understanding T-cell development. Such insights can be gained by directly observing developing T-cells within their environment under various conditions and following specific experimental manipulations. In the last decade, several model systems have been developed to address temporal and spatial aspects of T-cell development using imaging approaches. In this perspective article, we discuss the advantages and limitations of these systems and highlight a particularly powerful model that has been recently established. This model system enables the migratory behavior of all thymocytes to be studied simultaneously in a noninvasive and quantitative manner, making it possible to perform systems-level studies that reveal fundamental principles governing T-cell dynamics during development and in disease.
T 细胞的发育伴随着高度有序的迁移模式。淋巴祖细胞必须遵循精确的旅程;从造血组织开始,它们向胸腺移动,然后迁移到和离开不同的胸腺微环境,在那里它们接收分化为幼稚 T 细胞所需的信号和线索。了解这些细胞在哪里、何时以及如何做出定向“决策”是理解 T 细胞发育的关键。通过在各种条件下直接观察其环境中的发育中的 T 细胞并进行特定的实验操作,可以获得这些见解。在过去的十年中,已经开发了几种模型系统,以使用成像方法解决 T 细胞发育的时间和空间方面的问题。在这篇观点文章中,我们讨论了这些系统的优点和局限性,并强调了最近建立的一个特别强大的模型。该模型系统能够以非侵入性和定量的方式同时研究所有胸腺细胞的迁移行为,从而能够进行系统水平的研究,揭示发育过程中和疾病中控制 T 细胞动力学的基本原理。