University of Littoral Côte d'Opale, Unit of Environmental Chemistry and Interactions with Life, UCEIV EA4492, SFR Condorcet FR CNRS 3417, Dunkerque, France.
University of Littoral Côte d'Opale, Common Center of Measurements, CCM, Dunkerque, France.
Environ Pollut. 2019 Nov;254(Pt A):112933. doi: 10.1016/j.envpol.2019.07.101. Epub 2019 Jul 25.
Exposure to fine atmospheric Particulate Matter (PM) is one of the major environmental causes involved in the development of inflammatory lung diseases, such as chronic obstructive pulmonary disease (COPD) or asthma. When PM is penetrating in the pulmonary system, alveolar macrophages represent the first line of defense, in particular by triggering a pro-inflammatory response, and also by their ability to recruit infiltrating macrophages from the bone marrow. The aim of this in vitro study was to evaluate the gene expression and cytokine production involved in the toxicological and inflammatory responses of infiltrating macrophages, as well as the Extracellular Vesicles (EVs) production, after their exposure to PM. The ability of these EVs to convey information related to PM exposure from exposed macrophages to pulmonary epithelial cells was also evaluated. Infiltrating macrophages respond to fine particles exposure in a conventional manner, as their exposure to PM induced the expression of Xenobiotic Metabolizing Enzymes (XMEs) such as CYP1A1 and CYP1B1, the enzymes involved in oxidative stress SOD2, NQO1 and HMOX as well as pro-inflammatory cytokines in a dose-dependent manner. Exposure to PM also induced a greater release of EVs in a dose-dependent manner. In addition, the produced EVs were able to induce a pro-inflammatory phenotype on pulmonary epithelial cells, with the induction of the release of IL6 and TNFα proinflammatory cytokines. These results suggest that infiltrating macrophages participate in the pro-inflammatory response induced by PM exposure and that EVs could be involved in this mechanism.
大气细颗粒物(PM)暴露是引发炎症性肺部疾病(如慢性阻塞性肺疾病或哮喘)的主要环境因素之一。当 PM 穿透肺部系统时,肺泡巨噬细胞是第一道防线,特别是通过触发促炎反应,以及通过其从骨髓招募浸润巨噬细胞的能力。本体外研究旨在评估浸润性巨噬细胞的毒性和炎症反应所涉及的基因表达和细胞因子产生,以及 PM 暴露后细胞外囊泡(EVs)的产生。还评估了这些 EVs 将与 PM 暴露相关的信息从暴露的巨噬细胞传递到肺上皮细胞的能力。浸润性巨噬细胞以常规方式对细颗粒暴露做出反应,因为它们暴露于 PM 会诱导细胞色素 P450 家族 1 亚家族 A 成员 1(CYP1A1)和细胞色素 P450 家族 1 亚家族 B 成员 1(CYP1B1)等外源代谢酶(XMEs)的表达,这些酶参与氧化应激 SOD2、NQO1 和 HMOX 以及细胞因子的表达呈剂量依赖性。PM 暴露还会诱导 EVs 的释放呈剂量依赖性增加。此外,产生的 EVs 能够在上皮细胞上诱导促炎表型,诱导白细胞介素 6(IL6)和肿瘤坏死因子 α(TNFα)等促炎细胞因子的释放。这些结果表明,浸润性巨噬细胞参与 PM 暴露诱导的促炎反应,并且 EVs 可能参与这种机制。