CD14型
生物
细胞生物学
模式识别受体
炎症
发病机制
信号转导
先天免疫系统
受体
TLR2型
免疫学
NFAT公司
TLR4型
免疫系统
遗传学
基因
转录因子
作者
Zhenghao Wu,Zhenxiong Zhang,Zehua Lei,Ping Lei
标识
DOI:10.1016/j.cytogfr.2019.06.003
摘要
Human monocyte differentiation antigen CD14 is a pattern recognition receptor (PRR) that enhances innate immune responses. CD14 was first identified as a marker of monocytes to signal intracellular responses upon bacterial encounters. Given the absence of an intracellular tail, CD14 was doubted to have the signaling capacities. Later CD14 was confirmed as the TLR co-receptor for the detection of pathogen-associated molecular patterns. However, CD14 has been revealed as a multi-talented receptor. In last decade, CD14 was identified to activate NFAT to regulate the life cycle of myeloid cells in a TLR4-independent manner and to transport inflammatory lipids to induce phagocyte hyperactivation. And its influences on multiple related diseases have been further considered. In this review, we summarize advancements in the basic biology of the CD14 including its structure, binding ligands, signaling pathways, and its roles in the pathogenesis of inflammation, atherosclerosis, tumor and metabolic diseases. We also discuss the therapeutic potential of targeting the CD14 in related diseases.
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