体外实验研究COPD巨噬细胞的促炎活性

I. Sugaylo, D. Naumov, D. Gassan, O. Kotova, Y. Gorchakova
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介绍。慢性阻塞性肺疾病(COPD)是一种以不可逆气道阻塞和肺气肿为特征的严重进行性疾病。长期暴露于空气中有毒物质会引发不可逆的过程,导致巨噬细胞异常极化和吞噬功能缺陷,促炎性和抗炎性细胞因子失衡。的目标。探讨慢性阻塞性肺病患者巨噬细胞对促炎和抗炎刺激的反应特点。材料和方法。该研究包括8名COPD患者和6名对照受试者。所有人都接受了临床和功能检查,并采集了外周静脉血以分离单核细胞。用50 ng/mL的粒细胞-巨噬细胞集落刺激因子培养细胞6 d,然后分别加入100 ng/mL的大肠杆菌脂多糖(LPS)和20 ng/mL的重组人干扰素γ (IFN-γ)或20 ng/mL的白细胞介素4 (IL-4),将细胞极化为促炎(M1)和抗炎(M2)巨噬细胞。用流式细胞仪对培养基上清进行细胞因子分析。结果。在非极化状态(M0)下,COPD患者和对照组的细胞在细胞因子产生率上没有差异。与此同时,在LPS/IFN-γ刺激下,COPD患者促炎CXCL10较对照组增加更明显(104.5倍比41.6倍,p=0.04),相反,对照组抗炎IL-10的产生增加更大(99.6倍比30.5倍,p=0.06)。与健康组相比,IL-4对COPD巨噬细胞的影响伴随着IL-6、TNFα和IL-8的更明显下降。结论。COPD巨噬细胞的特点是对极化刺激的敏感性增加:在M1刺激下,我们观察到促炎活性增加,而在M2分化的条件下,促炎介质的抑制更为明显。
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Pro-inflammatory activity of COPD macrophages in the in vitro experiment
Introduction. Chronic obstructive pulmonary disease (COPD) is a severe, progressive disease characterized by irreversible airway obstruction and emphysema. Prolonged exposition to airborne toxicants triggers irreversible processes leading to aberrant polarization of macrophages and defective phagocytosis, imbalance of pro- and anti-inflammatory cytokines. Aim. To study the features of the reaction of macrophages in COPD patients to the action of pro- and anti-inflammatory stimuli. Materials and methods. The study included 8 COPD patients and 6 control subjects. All persons underwent clinical and functional examination and sampling of peripheral venous blood for the isolation of monocytes. Cells had been cultured with 50 ng/mL granulocyte-macrophage colony-stimulating factor for 6 days, and then were polarized into pro-inflammatory (M1) and anti-inflammatory (M2) macrophages by adding E. coli lipopolysaccharides (LPS) 100 ng/mL and recombinant human interferon gamma (IFN-γ) 20 ng/ml, or interleukin 4 (IL-4) 20 ng/ml, respectively. Cytokine analysis was performed in the culture medium supernatant by multiplex analysis on a flow cytometer. Results. In the non-polarized state (M0), cells of COPD patients and the control group did not differ in the rate of cytokine production. At the same time, under LPS/IFN-γ stimulation a more pronounced increase in pro-inflammatory CXCL10 was observed in patients with COPD as compared with the control group (104.5-fold vs. 41.6-fold, p=0.04), and in the control group, on the contrary, the production of anti-inflammatory IL-10 was increased to a greater extent (99.6-fold vs. 30.5- fold, p=0.06). The effect of IL-4 on COPD macrophages was accompanied by a more pronounced decrease in IL-6, TNFα and IL-8 as compared to the group of healthy subjects. Conclusion. COPD macrophages are characterized by increased sensitivity to polarizing stimuli: under M1 stimulation we observed increased pro-inflammatory activity and under conditions of M2 differentiation, on the contrary, more pronounced inhibition of pro-inflammatory mediators occurred. 
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