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G-CSF 和 GM-CSF 在囊性纤维化中发现的浓度下改变中性粒细胞功能。

G-CSF and GM-CSF Modify Neutrophil Functions at Concentrations found in Cystic Fibrosis.

机构信息

Department of Medical and Surgical Sciences, University of Foggia, Foggia, Italy.

Department of Biomedical Sciences and Human Oncology, Section of General Pathology, University of Bari, Bari, Italy.

出版信息

Sci Rep. 2019 Sep 10;9(1):12937. doi: 10.1038/s41598-019-49419-z.

Abstract

The role of colony stimulating factors (CSFs) in cystic fibrosis (CF) circulating neutrophils has not been thoroughly evaluated, considering that the neutrophil burden of lung inflammation in these subjects is very high. The aim of this study was to assess granulocyte-CSF (G-CSF) and granulocyte-macrophage-CSF (GM-CSF) levels in CF patients in various clinical conditions and how these cytokines impact on activation and priming of neutrophils. G-CSF and GM-CSF levels were measured in sputum and serum samples of stable CF patients (n = 21) and in CF patients with acute exacerbation before and after a course of antibiotic therapy (n = 19). CSFs were tested on non CF neutrophils to investigate their effects on reactive oxygen species (ROS) production, degranulation (CD66b, elastase, lactoferrin, MMP-9), and chemotaxis. At very low concentrations found in CF patients (0.005-0.1 ng/ml), both cytokines inhibited ROS production, while higher concentrations (1-5 ng/ml) exerted a stimulatory effect. While either CSF induced elastase and MMP-9 secretion, lactoferrin levels were increased only by G-CSF. Chemotaxis was inhibited by GM-CSF, but was increased by G-CSF. However, when present together at low concentrations, CSFs increased basal and fMLP-stimulated ROS production and chemotaxis. These results suggest the CSF levels that circulating neutrophils face before extravasating into the lungs of CF patients may enhance their function contributing to the airway damage.

摘要

集落刺激因子(CSFs)在囊性纤维化(CF)循环中性粒细胞中的作用尚未得到充分评估,因为这些患者肺部炎症的中性粒细胞负担非常高。本研究旨在评估不同临床情况下 CF 患者粒细胞集落刺激因子(G-CSF)和粒细胞-巨噬细胞集落刺激因子(GM-CSF)的水平,以及这些细胞因子如何影响中性粒细胞的激活和致敏。在稳定期 CF 患者(n=21)和 CF 患者急性加重期(n=19)的痰和血清样本中测量了 G-CSF 和 GM-CSF 水平,并在抗生素治疗前后进行了测量。在非 CF 中性粒细胞上测试了 CSFs,以研究它们对活性氧(ROS)产生、脱颗粒(CD66b、弹性蛋白酶、乳铁蛋白、MMP-9)和趋化性的影响。在 CF 患者中发现的非常低浓度(0.005-0.1ng/ml)下,两种细胞因子均抑制 ROS 产生,而较高浓度(1-5ng/ml)则产生刺激作用。虽然两种 CSF 都诱导弹性蛋白酶和 MMP-9 分泌,但乳铁蛋白水平仅由 G-CSF 增加。GM-CSF 抑制趋化性,但 G-CSF 增加趋化性。然而,当以低浓度同时存在时,CSFs 增加了基础和 fMLP 刺激的 ROS 产生和趋化性。这些结果表明,在渗出到 CF 患者肺部之前,循环中性粒细胞面临的 CSF 水平可能会增强其功能,从而导致气道损伤。

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