巨噬细胞和小胶质细胞极化:关注自噬依赖性重编程。

Svetlana G Zubova, Irina I Suvorova, Marina N Karpenko
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引用次数: 15

摘要

近年来,研究自噬的方法发生了很大的变化:从研究自噬机制的蛋白质成分到不同分子水平上的调控。自噬不仅被视为细胞中分离的降解过程本身,而且被视为在特定条件下被激活的某些信号通路的执行机制。此外,自噬开始被观察到是细胞重编程的关键组成部分,从一种表型状态到另一种表型状态的转变与先前的蛋白质停滞状态的快速降解有关。巨噬细胞和小胶质细胞表现出表型的多样性,反映了它们有效的表型可塑性能力。因此,了解自噬在巨噬细胞和小胶质细胞功能中的作用需要解决。在这篇综述中,我们关注自噬作为巨噬细胞和小胶质细胞极化的基本细胞内过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Macrophage and microglia polarization: focus on autophagy-dependent reprogramming.

The approach to the study of autophagy has been undergoing considerable change lately: from investigations of the protein components of autophagic machinery to its regulation at different molecular levels. Autophagy is being examinated not only as a separated degradative process per se in cells but as an executor mechanism of certain signaling pathways that converge on it, being activated under specific conditions. Additionally, autophagy is beginning to be observed as a key integral part of cellular reprogramming, the transition from one phenotypic state to another associated with rapid degradation of the previous proteostasis. Macrophages and microglia demonstrate a diversity of phenotypes reflecting their effective capability to phenotypic plasticity. Therefore, understanding the role of autophagy in macrophage and microglia functions needs to be addressed. In this review, we focus on autophagy as a fundamental intracellular process underlying macrophages and microglia polarization.

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