Center for Translational Ocular Immunology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA; Department of Ophthalmology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA; Schepens Eye Research Institute/Massachusetts Eye and Ear, Department of Ophthalmology, Harvard Medical School, Boston, MA, USA.
Center for Translational Ocular Immunology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA; Department of Ophthalmology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA.
Ocul Surf. 2020 Apr;18(2):277-285. doi: 10.1016/j.jtos.2020.02.005. Epub 2020 Feb 25.
Plasmacytoid dendritic cells (pDCs) constitute a unique population of bone marrow-derived cells that play a pivotal role in linking innate and adaptive immune responses. While peripheral tissues are typically devoid of pDCs during steady state, few tissues do host resident pDCs. In the current study, we aim to assess presence and distribution of pDCs in naïve murine limbus and bulbar conjunctiva. Immunofluorescence staining followed by confocal microscopy revealed that the naïve bulbar conjunctiva of wild-type mice hosts CD45 CD11c PDCA-1 pDCs. Flow cytometry confirmed the presence of resident pDCs in the bulbar conjunctiva through multiple additional markers, and showed that they express maturation markers, the T cell co-inhibitory molecules PD-L1 and B7-H3, and minor to negligible levels of T cell co-stimulatory molecules CD40, CD86, and ICAM-1. Epi-fluorescent microscopy of DPE-GFP×RAG1 transgenic mice with GFP-tagged pDCs indicated lower density of pDCs in the bulbar conjunctiva compared to the limbus. Further, intravital multiphoton microscopy revealed that resident pDCs accompany the limbal vessels and patrol the intravascular space. In vitro multiphoton microscopy showed that pDCs are attracted to human umbilical vein endothelial cells and interact with them during tube formation. In conclusion, our study shows that the limbus and bulbar conjunctiva are endowed with resident pDCs during steady state, which express maturation and classic T cell co-inhibitory molecules, engulf limbal vessels, and patrol intravascular spaces.
浆细胞样树突状细胞 (pDCs) 是骨髓来源的一类独特细胞群体,在连接固有免疫和适应性免疫应答中发挥关键作用。在静息状态下,外周组织通常缺乏 pDCs,但也有少数组织存在固有 pDCs。本研究旨在评估幼稚小鼠角膜缘和球结膜中 pDCs 的存在和分布。免疫荧光染色和共聚焦显微镜显示,野生型小鼠的幼稚球结膜存在 CD45+CD11c+PDCA-1+pDCs。流式细胞术通过多个额外的标记物证实了球结膜中存在固有 pDCs,并表明它们表达成熟标志物、T 细胞共抑制分子 PD-L1 和 B7-H3,以及微量至可忽略水平的 T 细胞共刺激分子 CD40、CD86 和 ICAM-1。具有 GFP 标记的 pDCs 的 DPE-GFP×RAG1 转基因小鼠的 epi-荧光显微镜表明,球结膜中的 pDCs 密度低于角膜缘。此外,活体多光子显微镜显示,固有 pDCs 伴随角膜缘血管,并在血管内空间巡逻。体外多光子显微镜显示,pDCs 被人脐静脉内皮细胞吸引,并在管形成过程中与之相互作用。总之,本研究表明,在静息状态下,角膜缘和球结膜存在固有 pDCs,它们表达成熟和经典的 T 细胞共抑制分子,吞噬角膜缘血管,并在血管内空间巡逻。