Department of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, WAO Center of Excellence, 80131 Naples, Italy.
Istituto di Scienze e Tecnologie per l'Energia e la Mobilità Sostenibili (STEMS)-CNR, 80125 Naples, Italy.
Environ Int. 2022 Aug;166:107395. doi: 10.1016/j.envint.2022.107395. Epub 2022 Jul 7.
The anthropogenic particulate matter (PM), suspended air dust that can be inhaled by humans and deposited in the lungs, is one of the main pollutants in the industrialized cities atmosphere. Recent studies have shown that PM has adverse effects on respiratory diseases. These effects are mainly due to the ultrafine particles (PM0.1, PM < 100 nm), which, thanks to their PM size, are efficiently deposited in nasal, tracheobronchial, and alveolar regions. Pulmonary macrophages are a heterogeneous cell population distributed in different lung compartments, whose role in inflammatory response to injury is of particular relevance. In this study, we investigated the effect of PM0.1 on Human Lung Macrophages (HLMs) activation evaluated as proinflammatory cytokines and chemokine release, Reactive Oxygen Species (ROS) production and intracellular Caconcentration ([Ca]). Furthermore, PM0.1, after removal of organic fraction, was fractionated in nanoparticles both smaller (NP20) and bigger (NP100) than 20 nm by a properlydeveloped analytical protocol, allowed isolating their individual contribution. Interestingly, while PM0.1 and NP20 induced stimulatory effects on HLM cytokines release, NP100 had not effect. In particular, PM0.1 induced IL-6, IL-1β, TNF-α, but not CXCL8, release from HLMs. Moreover, PM0.1, NP20 and NP100 did not induce β-glucuronidase release, a preformed mediator contained in HLMs. The long time necessary for cytokines release (18 h) suggested that PM0.1 and NP20 could induce ex-novo production of the tested mediators. Accordingly, after 6 h of incubation, PM0.1 and NP20 induced mRNA expression of IL-6, TNF-α and IL-1β. Moreover, NP20 induced ROS production and [Ca] increase in a time-dependent manner, without producing cytotoxicity. Collectively, the present data highlight the main proinflammatory role of NP20 among PM fractions. This is particularly of concern because this fraction is not currently covered by legal limits as it is not easily measured at the exhausts by the available technical methodologies, suggesting that it is mandatory to search for new monitoring techniques and strategies for limiting NP20 formation.
人为产生的颗粒物(PM)是一种可被人类吸入并沉积在肺部的悬浮空气尘埃,是工业化城市大气中的主要污染物之一。最近的研究表明,PM 对呼吸道疾病有不良影响。这些影响主要归因于超细颗粒(PM0.1,PM<100nm),由于其 PM 尺寸,这些颗粒可以有效地沉积在鼻腔、气管支气管和肺泡区域。肺巨噬细胞是一种异质细胞群体,分布在不同的肺区,其在炎症反应中的作用尤其重要。在这项研究中,我们研究了 PM0.1 对人肺巨噬细胞(HLMs)激活的影响,这种激活表现为促炎细胞因子和趋化因子的释放、活性氧物质(ROS)的产生和细胞内 Ca2+浓度([Ca2+]i)的变化。此外,PM0.1 在去除有机部分后,根据适当开发的分析方案,通过纳米颗粒分级为更小(NP20)和更大(NP100)的两种纳米颗粒(均小于 20nm),从而可以分离出它们各自的贡献。有趣的是,虽然 PM0.1 和 NP20 可刺激 HLMs 细胞因子的释放,但 NP100 没有效果。具体来说,PM0.1 诱导 HLMs 释放白细胞介素 6(IL-6)、白细胞介素 1β(IL-1β)和肿瘤坏死因子-α(TNF-α),但不诱导趋化因子 CXCL8 的释放。此外,PM0.1、NP20 和 NP100 均未诱导 HLMs 预先存在的β-葡糖苷酸酶的释放。细胞因子释放所需的时间较长(18 小时)表明,PM0.1 和 NP20 可能诱导了所测试介质的从头合成。因此,在孵育 6 小时后,PM0.1 和 NP20 诱导了 IL-6、TNF-α 和 IL-1β 的 mRNA 表达。此外,NP20 以时间依赖性方式诱导 ROS 的产生和[Ca2+]i 的增加,而不产生细胞毒性。总之,这些数据突出了 PM 各部分中 NP20 的主要促炎作用。这一点尤其令人关注,因为由于该部分目前不受法律限制,因此不易通过现有技术方法在废气中进行测量,这表明必须寻找新的监测技术和策略来限制 NP20 的形成。