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人中性粒细胞自噬机制的调控。

Regulation of the autophagic machinery in human neutrophils.

机构信息

First Department of Internal Medicine, Democritus University of Thrace, Alexandroupolis, Greece.

出版信息

Eur J Immunol. 2010 May;40(5):1461-72. doi: 10.1002/eji.200940025.

Abstract

The induction of the autophagy machinery, a process for the catabolism of cytosolic proteins and organelles, constitutes a crucial mechanism in innate immunity. However, the involvement of autophagy in human neutrophils and the possible inducers of this process have not been completely elucidated. In this study, the induction of autophagy was examined in human neutrophils treated with various activators and detected by the formation of acidified autophagosomes through monodansylcadaverine staining and via LC-3B conversion screened by immunoblotting and immunofluorescence confocal microscopy. In addition, the expression of the ATG genes was assessed by real-time RT-PCR. We provide evidence that autophagy is implicated in human neutrophils in both a phagocytosis-independent (rapamycin, TLR agonists, PMA) and phagocytosis (Escherichia coli)-dependent initiation manner. ROS activation is a positive mechanism for autophagy induction in the case of PMA, TLR activation and phagocytosis. Furthermore, LC3B gene expression was uniformly upregulated, indicating a transcriptional level of regulation for the autophagic machinery. This study provides a stepping stone toward further investigation of autophagy in neutrophil-driven inflammatory disorders.

摘要

自噬机制的诱导,即细胞溶质蛋白和细胞器的分解代谢过程,是先天免疫中的一个关键机制。然而,自噬在人类中性粒细胞中的参与情况以及该过程的可能诱导剂尚未完全阐明。在这项研究中,通过单丹磺酰尸胺染色检测酸性自噬体的形成,并通过免疫印迹和免疫荧光共聚焦显微镜筛选 LC-3B 转化,检查了各种激活剂处理的人类中性粒细胞中自噬的诱导。此外,通过实时 RT-PCR 评估了 ATG 基因的表达。我们提供的证据表明,自噬参与了人类中性粒细胞的吞噬作用(雷帕霉素、TLR 激动剂、PMA)和非吞噬作用(大肠杆菌)的启动方式。在 PMA、TLR 激活和吞噬作用的情况下,ROS 激活是自噬诱导的正向机制。此外,LC3B 基因表达均上调,表明自噬机制的转录水平调节。这项研究为进一步研究中性粒细胞驱动的炎症性疾病中的自噬提供了一个起点。

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