Pavanello Sofia, Bonzini Matteo, Angelici Laura, Motta Valeria, Pergoli Laura, Hoxha Mirjam, Cantone Laura, Pesatori Angela Cecilia, Apostoli Pietro, Tripodi Armando, Baccarelli Andrea, Bollati Valentina
Occupational Medicine, Department of Cardiac, Thoracic and Vascular Sciences, Università degli Studi di Padova, 35128, Padova, Italy.
EPIGET - Epidemiology, Epigenetics and Toxicology Lab, Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milan, Italy; Epidemiology Unit, Department of Preventive Medicine, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Toxicol Lett. 2016 Sep 30;259:143-150. doi: 10.1016/j.toxlet.2016.08.002. Epub 2016 Aug 6.
Continuous exposure to particulate air pollution (PM) is a serious worldwide threat to public health as it coherently links with increased morbidity and mortality of cardiorespiratory diseases (CRD), and of type 2 diabetes (T2D). Extracellular vesicles (EVs) are circular plasma membrane fragments released from human cells that transfer microRNAs between tissues. In the present work it was explored the hypothesis that EVs with their encapsulated microRNAs (EVmiRNAs) contents might mediate PM effects by triggering key pathways in CRD and T2D.
Expression of EVmiRNAs analyzed by real-time PCR was correlated with oxidative stress, coagulation and inflammation markers, from healthy steel plant workers (n=55) with a well-characterized exposure to PM and PM-associated metals. All p-values were adjusted for multiple comparisons. In-silico Ingenuity Pathway Analysis (IPA) was performed to identify biological pathways regulated by PM-associated EVmiRNAs.
Increased expression in 17 EVmiRNAs is associated with PM and metal exposure (p<0.01). Mir-196b that tops the list, being related to 9 different metals, is fundamental in insulin biosynthesis, however three (miR-302b, miR-200c, miR-30d) out of these 17 EVmiRNAs are in turn also related to disruptions (p<0.01) in inflammatory and coagulation markers.
The study's findings support the hypothesis that adverse cardiovascular and metabolic effects stemming from inhalation exposures in particular to PM metallic component may be mediated by EVmiRNAs that target key factors in the inflammation, coagulation and glucose homeostasis pathways.
持续暴露于空气中的颗粒物污染(PM)是一个严重的全球性公共卫生威胁,因为它与心血管呼吸系统疾病(CRD)和2型糖尿病(T2D)的发病率和死亡率增加密切相关。细胞外囊泡(EVs)是从人类细胞释放的圆形质膜片段,可在组织间转移微小RNA。在本研究中,我们探讨了一个假设,即携带其包裹的微小RNA(EVmiRNAs)的细胞外囊泡可能通过触发CRD和T2D中的关键途径来介导PM的影响。
通过实时PCR分析的EVmiRNAs表达与氧化应激、凝血和炎症标志物相关,这些标志物来自55名健康的钢铁厂工人,他们对PM和与PM相关的金属有明确的暴露情况。所有p值均针对多重比较进行了调整。进行了计算机 Ingenuity 通路分析(IPA),以识别由与PM相关的EVmiRNAs调节的生物通路。
17种EVmiRNAs的表达增加与PM和金属暴露相关(p<0.01)。排名第一的mir-196b与9种不同的金属相关,在胰岛素生物合成中起重要作用,然而这17种EVmiRNAs中的三种(miR-302b、miR-200c、miR-30d)反过来也与炎症和凝血标志物的破坏相关(p<0.01)。
该研究结果支持以下假设:吸入暴露尤其是PM金属成分所产生的不良心血管和代谢影响可能由靶向炎症、凝血和葡萄糖稳态途径中的关键因子的EVmiRNAs介导。