色素沉着
白癜风
色素减退
真皮
黑色素
医学
黑素体
色素沉着障碍
巨噬细胞
皮肤病科
肿瘤坏死因子α
免疫学
黑素细胞
细胞因子
病理
黑色素瘤
吞噬作用
小眼畸形相关转录因子
免疫系统
生物
分泌物
皮肤类型
白细胞介素
干扰素
痣
作者
Huiyi Yao,Xingyue Gao,Wenzhong Xiang
标识
DOI:10.1111/1346-8138.70065
摘要
ABSTRACT Diseases associated with skin pigmentation include hyperpigmentation and hypopigmentation. Macrophages are involved in melanogenesis and the development of skin pigmentary disorders, and they affect the production and distribution of melanin mainly through phagocytosis and secretion. They can either phagocytose melanin and deposit it in the dermis or secrete a variety of cytokines like interferon (IFN)‐ γ , tumor necrosis factor (TNF), granulocyte‐macrophage colony‐stimulating factor (GM‐CSF), and some interleukins (ILs) such as IL‐1, IL‐6, IL‐8, and IL‐18. The interaction between macrophages and other cells is responsible for the secretion of these cytokines. Macrophages can also promote pigmentation in hyperpigmentation disorders, such as post‐inflammatory hyperpigmentation (PIH), drug‐induced pigmentation (DIP), senile lentigo (SL), and melasma, as well as hypopigmentation disorders such as vitiligo and halo nevus (HN). In this review, we summarize the role of macrophages in the development of pigmentary diseases and provide new insights for the identification of potential targets for pigmentary diseases.
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