微管组织中心
高尔基体
免疫突触
细胞生物学
溶解循环
生物
免疫系统
化学
T细胞
细胞
病毒
中心体
病毒学
T细胞受体
免疫学
细胞周期
遗传学
内质网
作者
Meritxell Roig-Martínez,Elena Saavedra-López,Paola V. Casanova,George P. Cribaro,Carlos Barcia
出处
期刊:Results and problems in cell differentiation
日期:2019-01-01
卷期号:: 223-231
被引量:8
标识
DOI:10.1007/978-3-030-23173-6_9
摘要
T cells effectively explore the tissue in search for antigens. When activated, they dedicate a big amount of energy and resources to arrange a complex structure called immunological synapse (IS), containing a particular distribution of molecules defined as supramolecular activation clusters (SMACs), and become polarized toward the target cell in a manner that channels the information specifically. This arrangement is symmetrical and requires the polarization of the MTOC and the Golgi to be operational, especially for the proper delivery of lytic granules and the recycling of molecules three dimensionally segregated at the clustered interface. Alternatively, after the productive encounter, T cells need to rearrange again to newly navigate through the tissue, changing back to a motile state called immunological kinapse (IK). In this IK state, the MTOC and the Golgi apparatus are repositioned and recruited at the back of the T cell to facilitate motility, while the established symmetry of the elements of the SMACs is broken and distributed in a different pattern. Both states, IS and IK, are interchangeable and are mainly orchestrated by the MTOC/Golgi complex, being critical for an effective immune response.
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