依赖于冠状病毒蛋白 1 的细胞密度感应和外周 T 细胞群规模的调节

Tohnyui Ndinyanka Fabrice, Mayumi Mori, Jean Pieters
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引用次数: 0

摘要

外周 T 细胞的建立和维持对于确保适当的免疫力非常重要。在哺乳动物中,T 细胞是在胸腺中产生的,然后在生命早期播种到外周,此后胸腺逐渐萎缩,影响了新 T 细胞的产生。然而,外周 T 细胞终生保持着大致相同的细胞数量。由此产生的问题是:是什么机制使循环 T 细胞保持适当的数量,确保 T 细胞数量不会过低或过高?在此,我们重点介绍最近的一项研究,该研究表明,冠状蛋白 1(进化保守的冠状蛋白家族成员)在使 T 细胞达到并维持其适当的细胞数量方面起着关键作用。研究发现,这种控制细胞数量的途径在变形虫、小鼠和人类中都是保守的。我们提出,冠状蛋白 1 是细胞内在通路的一个组成部分,它将细胞密度信息与促生存信号结合起来,从而调节外周 T 细胞的适当数量。
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Coronin 1-dependent cell density sensing and regulation of the peripheral T cell population size
The establishment and maintenance of peripheral T cells is important to ensure appropriate immunity. In mammals, T cells are produced in the thymus before seeding the periphery early in life, and thereafter progressive thymus involution impairs new T cell production. Yet, peripheral T cells are maintained lifelong at approximately similar cell numbers. The question thus arises: what are the mechanisms that enable the maintenance of the appropriate number of circulating T cells, ensuring that T cell numbers are neither too low nor too high? Here, we highlight recent research suggesting a key role for coronin 1, a member of the evolutionarily conserved family of coronin proteins, in both allowing T cells to reach as well as maintain their appropriate cell population size. This cell population size controlling pathway was found to be conserved in amoeba, mice and human. We propose that coronin 1 is an integral part of a cell-intrinsic pathway that couples cell density information with prosurvival signalling thereby regulating the appropriate number of peripheral T cells.
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CiteScore
2.20
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0.00%
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审稿时长
9 weeks
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