细胞生物学
细胞毒性T细胞
跨膜蛋白
抗原
生物
嵌合抗原受体
免疫系统
受体
膜蛋白
细胞
T细胞
化学
免疫学
膜
生物化学
体外
作者
Stefano Barbera,Matthijs J. A. Schuiling,Nathaniel A. Sanjaya,Ilkka Pietilä,Tina Sarén,Magnus Essand,Anna Dimberg
出处
期刊:Science immunology
[American Association for the Advancement of Science]
日期:2025-01-31
卷期号:10 (103)
被引量:1
标识
DOI:10.1126/sciimmunol.ado2054
摘要
Trogocytosis is an exchange of membrane-associated molecules between cells that can either halt or boost immune responses. However, the mechanism that regulates trogocytosis in T cells and its consequences are not yet clear. Here, we demonstrate that T cells can exchange chimeric antigen receptors (CARs) by trogocytosis, thereby arming recipient T cells with the capacity to respond to tumor antigens by up-regulating proteins associated with a cytotoxic response and killing of target cells. We demonstrate that although trogocytosis is dependent on cell-cell contact, the exchange of a specific cell membrane protein does not require a cognate binding partner on the surface of recipient cells. Instead, the probability that a protein is exchanged by trogocytosis is determined by its transmembrane domain. This finding opens new avenues for modulating this process in CAR-T cells.
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