趋化因子
生物
CXCL16型
抗原提呈细胞
CCL5
树突状细胞
T细胞
细胞生物学
CX3CL1型
CD11c公司
免疫学
巨噬细胞
脾脏
免疫系统
分子生物学
趋化因子受体
体外
白细胞介素2受体
表型
生物化学
基因
作者
Nobuo Kanazawa,Tomoyuki Nakamura,Kei Tashiro,Masamichi Muramatsu,Kazumasa Morita,Kozo Yoneda,Kayo Inaba,Sadao Imamura,Tasuku Honjo
标识
DOI:10.1002/(sici)1521-4141(199906)29:06<1925::aid-immu1925>3.0.co;2-u
摘要
Dendritic cells (DC) are a system of antigen-presenting cells specialized in interaction with T cells. Recently it has been reported that DC can produce CC (β) chemokines that attract T cells. In this study we isolated mouse fractalkine and macrophage-derived chemokine (MDC) belonging to CX3C (δ) and CC chemokine families, respectively, from bone marrow-derived mature DC. While expression of fractalkine, which has so far been only examined in the brain and in vitro endothelial cells so far, was rather ubiquitous, MDC, which has been reported to be synthesized by macrophages and DC, was expressed specifically in the thymus and lymphnode. This is the first report that indicates fractalkine expression by DC. Expression of fractalkine and MDC mRNA increased with maturation of DC during in vitro culture of bone marrow cells. Spleen- and epidermis-derived mature DC in culture also expressed these chemokines. Furthermore, their expression was detected selectively by Northern hybridization in CD11c+ B220– DC freshly purified from lymph nodes, and in large stellate cells in the lymph node T cell areas by in situ hybridization. Conditioned media of 293T cells transfected with these chemokine cDNA were chemotactic to Con A-activated splenic T cells as well as the mouse T cell line EL4. In conclusion, while fractalkine and MDC belong to different families of chemokines, both may be involved in recruitment of T cells for interaction with mature DC in the immune response.
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