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Fc gamma R-mediated phagocytosis

KEGG ID: hsa04666

中文名称

CRY 和 PER 蛋白的降解

通路描述

为了在早晨由 BMAL1:CLOCK 启动的新一轮转录,CRY1、CRY2 和 PER1、PER2、PER3(BMAL:CLOCK 的抑制子)在夜间被 SCF E3 连接酶复合物泛素化,随后被 26S 蛋白酶体降解。BTRC、FBXW11:CUL1:SKP1:RBX1 E3 连接酶复合物在细胞质中泛素化磷酸化的 PER1、PER2 和可能 PER3(Shirogane 等 2005,基于小鼠同源物 Reischl 等 2007、Ohsaki 等 2008 推断),FBXL3:CUL1:SKP1:RBX1 E3 连接酶复合物在细胞核中泛素化 CRY1 和 CRY2(基于小鼠同源物 Busino 等 2007、Hirano 等 2013、Yoo 等 2013 推断),而 FBXL21 通过未表征的机制抑制 FBXL3 在核内的泛素化(基于小鼠同源物 Hirano 等 2013、Yoo 等 2013 推断)。
英文描述
Phagocytosis plays an essential role in host-defense mechanisms through the uptake and destruction of infectious pathogens. Specialized cell types including macrophages, neutrophils, and monocytes take part in this process in higher organisms. After opsonization with antibodies (IgG), foreign extracellular materials are recognized by Fc gamma receptors. Cross-linking of Fc gamma receptors initiates a variety of signals mediated by tyrosine phosphorylation of multiple proteins, which lead through the actin cytoskeleton rearrangements and membrane remodeling to the formation of phagosomes. Nascent phagosomes undergo a process of maturation that involves fusion with lysosomes. The acquisition of lysosomal proteases and release of reactive oxygen species are crucial for digestion of engulfed materials in phagosomes.

所含基因

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