CD80
CD11c公司
CD40
细胞生物学
抗原提呈细胞
内体
树突状细胞
化学
CD86
T细胞
过继性细胞移植
白细胞介素2受体
生物物理学
生物
免疫系统
细胞毒性T细胞
体外
生物化学
细胞内
免疫学
表型
基因
作者
Tianpei He,Chaoke Tang,Yongqing Liu,Zhenmin Ye,Xiaochu Wu,Yangdou Wei,Terence Moyana,Jim Xiang
标识
DOI:10.1016/j.bbrc.2007.05.099
摘要
The acquisition of dendritic cell (DC) molecules by T cells has been previously reported. However, it remains unclear whether the transfer is only mono- or bidirectional. In this study, we incubated CMFDA-labeled ovalbumin (OVA)-pulsed DC2.4 (DC2.4(OVA)) cells with Dil-labeled OT II CD4(+) T cells and analyzed the potential bidirectional molecule transfer. We also assessed the distribution of internalized membrane using two engineered DC2.4/Ia(b)GFP and MF4/TCRCFP DC lines. Our findings showed that membrane molecule transfer is bidirectional. CD4(+) T cells acquired Ia(b), CD11c, CD40, and CD80 from DC2.4(OVA) cells, and conversely DC2.4(OVA) cells took up CD4, CD25, CD69, and T cell receptor from T cells. The internalized molecules acquired by T cells and DCs mostly localized in endosomes and lysosomes, respectively. Taken together, this study demonstrated a novel phenomenon of bidirectional membrane molecule transfer between DCs and T cells.
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