Jin Shiying, Lei Xuan, Singh Sonali, Enk Alexander, Mahnke Karsten
Department of Dermatology, University Hospital Heidelberg, Heidelberg, Germany.
Immunology. 2025 Oct;176(2):237-249. doi: 10.1111/imm.13958. Epub 2025 Jun 4.
The surface molecule DEC205 (CD205) is well-characterised in murine dendritic cells (DCs) as an antigen uptake receptor. However, recent studies have also identified its expression in other leukocytes, including B cells and neutrophils. In B cells, DEC205 functions as an endocytic receptor, similar to its role in DCs. Since neutrophils are not professional antigen-presenting cells, we sought to investigate the functions of DEC205 beyond endocytosis. Analysis of cell surface expression of DEC205 in neutrophils at different maturation stages and anatomical locations revealed its downregulation upon in vitro activation and during tissue infiltration, such as in skin inflammation and thioglycolate-induced peritonitis. In DEC205-deficient (DEC205) mice, neutrophils exhibited reduced migration in Boyden chamber assays and impaired accumulation in the peritoneum, along with decreased adhesion to extracellular matrix proteins. These findings suggest that, beyond its established role as an antigen uptake receptor in antigen-presenting cells, DEC205 may serve as a marker for early-stage neutrophils with the capacity to migrate and infiltrate tissues.
表面分子DEC205(CD205)在小鼠树突状细胞(DC)中作为抗原摄取受体已得到充分表征。然而,最近的研究也发现它在包括B细胞和中性粒细胞在内的其他白细胞中表达。在B细胞中,DEC205作为一种内吞受体发挥作用,与其在DC中的作用类似。由于中性粒细胞不是专职抗原呈递细胞,我们试图研究DEC205在内吞作用之外的功能。对不同成熟阶段和解剖位置的中性粒细胞中DEC205的细胞表面表达分析显示,在体外激活时以及在组织浸润(如皮肤炎症和巯基乙酸诱导的腹膜炎)期间,其表达下调。在DEC205缺陷(DEC205 -/-)小鼠中,中性粒细胞在博伊登室试验中迁移减少,在腹膜中的聚集受损,同时对细胞外基质蛋白的粘附也减少。这些发现表明,除了其在抗原呈递细胞中作为抗原摄取受体的既定作用外,DEC205可能作为具有迁移和浸润组织能力的早期中性粒细胞的标志物。