一种新的适应蛋白调节T细胞接触中的受体模式和细胞骨极性
M L Dustin1, M W Olszowy, A D Holdorf
1Department of Pathology and Center for Immunology, Washington University School of Medicine, Saint Louis, Missouri 63110, USA.
Cell
|September 19, 1998
概括
T细胞的识别涉及到专门的细胞结. CD2参与触发蛋白质分离,聚类和细胞骨变化,由新型CD2AP蛋白质与细胞骨连接受体进行介导.
科学领域:
- 免疫学 免疫学 免疫学
- 细胞生物学 细胞生物学
- 生物化学 生化学
背景情况:
- 对抗原的T细胞识别需要专门的细胞-细胞结.
- 在这些结点的蛋白质招募和排除是关键的,但不太了解.
- 粘附分子CD2在T细胞-APC相互作用中发挥作用.
研究的目的:
- 研究调节T细胞-APC接口中的蛋白质组织的机制.
- 识别参与CD2介导信号传递和细胞骨重组的蛋白质.
主要方法:
- 研究了CD2连接体对蛋白质分布和细胞形态学的影响.
- 研究了CD2细胞质域在这些过程中的作用.
- 鉴定和描述了一种新型含SH3的蛋白质CD2AP.
主要成果:
- CD2参与启动了蛋白质分离,CD2聚类和细胞骨两极分化.
- 蛋白质分离独立于CD2细胞质域.
- CD2聚类和细胞骨两极化需要CD2AP与CD2细胞质域相互作用.
结论:
- CD2AP是一种新型蛋白质,对CD2介导的T细胞-APC结形成至关重要.
- CD2AP将粘附受体与细胞骨连接在一起,从而促进受体模式.
- 了解CD2AP功能,可以了解T细胞激活和免疫突触形成.
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