吞噬体
吞噬作用
生物
细胞生物学
先天免疫系统
内吞循环
内质网
获得性免疫系统
抗原呈递
主要组织相容性复合体
细胞器
内吞作用
免疫系统
免疫学
生物化学
细胞
T细胞
作者
Isabelle Jutras,Michel Desjardins
标识
DOI:10.1146/annurev.cellbio.20.010403.102755
摘要
Phagocytosis, the process by which cells engulf large particles, requires a substantial contribution of membranes. Recent studies have revealed that intracellular compartments, including endocytic organelles and the endoplasmic reticulum (ER), can engage in fusion events with the plasma membrane at the sites of nascent phagosomes. The finding that ER proteins are delivered to phagosomes, where degraded peptides are loaded onto major histocompatibility complex (MHC) class II molecules, has significantly enhanced our understanding of the immune functions associated with these organelles. Although it is well known that pathogens are killed in phagosomes, the contribution of ER proteins to phagosomes has provided a novel pathway for the loading of exogenous peptides onto MHC class I molecules, a process known as cross-presentation. Thus, phagocytosis has evolved from a nutritional function in unicellular organisms to play key roles in both innate and adaptive immunity in vertebrates.
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