Department of Ophthalmology, Hadassah-Hebrew University Medical Center, 91120, Jerusalem, Israel,
Adv Exp Med Biol. 2014;801:199-205. doi: 10.1007/978-1-4614-3209-8_26.
White blood cells, particularly monocytes and their descendants, macrophages, have been implicated in age-related macular degeneration (AMD) pathology. In this minireview, we describe the current knowledge of monocyte and macrophage involvement in AMD. Chemokine receptors present on these cells such as CCR1, CCR2, and CX3CR1, and their roles in monocyte/macrophage recruitment to sites of injury and inflammation in the context of AMD will be reviewed. Mice models for perturbation of chemokine receptors that recapitulate some of the features of AMD are also described. The body of evidence from human and rodent studies at this point in time suggests that monocyte and macrophages may modulate the course of AMD.
白细胞,尤其是单核细胞及其后代巨噬细胞,已被牵涉到年龄相关性黄斑变性(AMD)的发病机制中。在这篇综述中,我们描述了单核细胞和巨噬细胞在 AMD 中的作用的最新知识。我们将回顾这些细胞上存在的趋化因子受体,如 CCR1、CCR2 和 CX3CR1,以及它们在 AMD 背景下单核细胞/巨噬细胞向损伤和炎症部位募集中的作用。我们还描述了用于模拟 AMD 某些特征的趋化因子受体扰动的小鼠模型。从目前的人类和啮齿动物研究来看,这些证据表明单核细胞和巨噬细胞可能调节 AMD 的病程。