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在巨噬细胞分化过程中几丁质酶 3 的调节作用。

Modulation of chitotriosidase during macrophage differentiation.

机构信息

Department of Bio-medical Sciences, University of Catania, Via Androne, 83, 95124, Catania, Italy.

出版信息

Cell Biochem Biophys. 2013 Jun;66(2):239-47. doi: 10.1007/s12013-012-9471-x.

DOI:10.1007/s12013-012-9471-x
PMID:23152091
Abstract

Macrophages as a principal component of immune system play an important role in the initiation, modulation, and final activation of the immune response against pathogens. Upon stimulation with different cytokines, macrophages can undergo classical or alternative activation to become M1 or M2 macrophages, which have different functions during infections. Although chitotriosidase is widely accepted as a marker of activated macrophages and is thought to participate in innate immunity, particularly in defense mechanisms against chitin containing pathogens, little is known about its expression during macrophages full maturation and polarization. In this study we analyzed CHIT-1 modulation during monocyte-to-macrophage maturation and during their polarization. The levels of CHIT-1 expression was investigated in human monocytes obtained from buffy coat of healthy volunteers, polarized to classically activated macrophages (or M1), whose prototypical activating stimuli are interferon-γ and lipopolysaccharide, and alternatively activated macrophages (or M2) obtained by interleukin-4 exposure by real-time PCR and by Western blot analysis. During monocyte-macrophage differentiation both protein synthesis and mRNA analysis showed that CHIT-1 rises significantly and is modulated in M1 and M2 macrophages.Our results demonstrated that variations of CHIT-1 production are strikingly associated with macrophages polarization, indicating a different rule of this enzyme in the specialized macrophages.

摘要

巨噬细胞作为免疫系统的主要成分,在针对病原体的免疫反应的启动、调节和最终激活中发挥重要作用。巨噬细胞在受到不同细胞因子刺激后,可以发生经典或替代激活,成为 M1 或 M2 巨噬细胞,它们在感染过程中具有不同的功能。虽然几丁质酶 1(chitotriosidase-1,CHIT-1)被广泛认为是激活巨噬细胞的标志物,并被认为参与先天免疫,特别是防御含有几丁质的病原体的机制,但对于其在巨噬细胞完全成熟和极化过程中的表达知之甚少。在这项研究中,我们分析了单核细胞向巨噬细胞成熟过程中和极化过程中 CHIT-1 的调节。通过实时 PCR 和 Western blot 分析,检测了从健康志愿者的白细胞层中获得的人单核细胞、经干扰素-γ和脂多糖经典激活(或 M1)的巨噬细胞、经白细胞介素-4 暴露的替代激活(或 M2)巨噬细胞中 CHIT-1 的表达水平。在单核细胞-巨噬细胞分化过程中,蛋白质合成和 mRNA 分析均表明 CHIT-1 显著升高,并在 M1 和 M2 巨噬细胞中受到调节。我们的研究结果表明,CHIT-1 产生的变化与巨噬细胞极化密切相关,表明该酶在特化巨噬细胞中有不同的规律。

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