细胞生物学
生物
免疫系统
人口
炎症
T细胞
细胞
免疫学
遗传学
医学
环境卫生
作者
Yury P. Rubtsov,Rachel Niec,Steven Z. Josefowicz,Li Li,Jaime R. Darce,Diane Mathis,Christophe Benoist,Alexander Y. Rudensky
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2010-09-24
卷期号:329 (5999): 1667-1671
被引量:633
标识
DOI:10.1126/science.1191996
摘要
Tissue maintenance and homeostasis can be achieved through the replacement of dying cells by differentiating precursors or self-renewal of terminally differentiated cells or relies heavily on cellular longevity in poorly regenerating tissues. Regulatory T cells (T(reg) cells) represent an actively dividing cell population with critical function in suppression of lethal immune-mediated inflammation. The plasticity of T(reg) cells has been actively debated because it could factor importantly in protective immunity or autoimmunity. By using inducible labeling and tracking of T(reg) cell fate in vivo, or transfers of highly purified T(reg) cells, we have demonstrated notable stability of this cell population under physiologic and inflammatory conditions. Our results suggest that self-renewal of mature T(reg) cells serves as a major mechanism of maintenance of the T(reg) cell lineage in adult mice.
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