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M1/M2 巨噬细胞极化在原发性干燥综合征中的作用。

The role of M1/M2 macrophage polarization in primary Sjogren's syndrome.

机构信息

Department of Rheumatology, The Second Affiliated Hospital of Zhejiang University School of Medicine, No.88 Jiefang Road, Hangzhou, 310009, P.R. China.

出版信息

Arthritis Res Ther. 2024 May 14;26(1):101. doi: 10.1186/s13075-024-03340-7.

Abstract

BACKGROUND

The purpose of this study was to investigate the role of macrophage polarization in the pathogenesis of primary Sjogren's syndrome (pSS).

METHODS

Peripheral venous blood samples were collected from 30 patients with pSS and 30 healthy controls. Minor salivary gland samples were abtainted from 10 of these patients and 10 non-pSS controls whose minor salivary gland didn't fulfill the classification criteria for pSS. Enzyme-linked immuno sorbent assay was used to examine the serum concentration of M1/M2 macrophage related cytokines (TNF-a, IL-6, IL-23, IL-4, IL-10 and TGF-β). Flow cytometry was used to examine the numbers of CD86 M1 macrophages and CD206 M2 macrophages in peripheral blood mononuclear cells (PBMCs). Immunofluorescence was used to test the infiltration of macrophages in minor salivary glands.

RESULTS

This study observed a significant increase in pSS patients both in the numbers of M1 macrophages in peripheral blood and serum levels of M1-related pro-inflammatory cytokines (IL-6, IL-23 and TNF-α). Conversely, M2 macrophages were downregulated in the peripheral blood of pSS patients. Similarly, in the minor salivary glands of pSS patients, the expression of M1 macrophages was increased, and that of M2 macrophages was decreased. Furthermore, a significantly positive correlation was found between the proportions of M1 macrophages in PBMCs and serum levels of IgG and RF.

CONCLUSIONS

This study reveals the presence of an significant imbalance in M1/M2 macrophages in pSS patients. The M1 polarization of macrophages may play an central role in the pathogenesis of pSS.

摘要

背景

本研究旨在探讨巨噬细胞极化在原发性干燥综合征(pSS)发病机制中的作用。

方法

收集 30 例 pSS 患者和 30 例健康对照者的外周静脉血样本。从其中 10 例 pSS 患者和 10 例非 pSS 对照者(其小唾液腺未满足 pSS 的分类标准)中获得小唾液腺样本。采用酶联免疫吸附试验检测 M1/M2 巨噬细胞相关细胞因子(TNF-a、IL-6、IL-23、IL-4、IL-10 和 TGF-β)的血清浓度。采用流式细胞术检测外周血单个核细胞(PBMC)中 CD86 M1 巨噬细胞和 CD206 M2 巨噬细胞的数量。采用免疫荧光法检测小唾液腺中巨噬细胞的浸润情况。

结果

本研究观察到 pSS 患者外周血 M1 巨噬细胞数量和 M1 相关促炎细胞因子(IL-6、IL-23 和 TNF-α)的血清水平显著增加。相反,pSS 患者外周血中 M2 巨噬细胞下调。同样,在 pSS 患者的小唾液腺中,M1 巨噬细胞的表达增加,M2 巨噬细胞的表达减少。此外,还发现 PBMC 中 M1 巨噬细胞的比例与 IgG 和 RF 的血清水平之间存在显著正相关。

结论

本研究揭示了 pSS 患者存在 M1/M2 巨噬细胞显著失衡。巨噬细胞的 M1 极化可能在 pSS 的发病机制中起核心作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bbd/11092035/b04a44d7e4ee/13075_2024_3340_Fig1_HTML.jpg

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