Department of Respiratory and Critical Care Medicine, Peking University First Hospital, Beijing, China.
Jiangsu Provincial Key Laboratory of Geriatrics, Department of Geriatrics, the First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Ecotoxicol Environ Saf. 2021 Jun 1;215:112127. doi: 10.1016/j.ecoenv.2021.112127. Epub 2021 Mar 11.
Numerous epidemiological studies have demonstrated that chronic PM2.5 exposure was associated with the lung carcinogenesis without known potential mechanisms. Exosomes-derived non-coding RNAs, including miRNAs, are proposed to play critical role in the occurrence and development of malignant diseases. So identification of exosomes-derived miRNAs could help us to better understand the molecular toxicity of PM2.5-induced lung cancer. Establishment chronic exposure animal and cell model with PM2.5 was conducted as before. HE staining was used for estimating the histological alternations of lungs in vivo. The expressions of EMT markers in vivo and vitro were quantified by Western blot. Then the exosomes in cell culture supernatant were extracted and the involved miRNAs were extracted and sequenced. The different expression level of miRNAs were verified by RT-PCR. Chronic PM2.5 exposure induced bronchial epithelial cell atypical hyperplasia and massive macrophage infiltration. PM2.5 exposure induce EMT event in vivo and vitro indicated as increased expression of Vimentin and decreased expression of E-cadherin. And five passages of PM2.5 stimulation also induced the release of rich and extractable exosomes in the cell culture supernatant in vitro. Through sequencing, there were differentially expressed 36 miRNAs between PM2.5 chronic exposed and control groups with 1.5-fold and greater differences. Among them, there were 30 exosome-miRNAs upregulated and 6 downregulated expression by PM2.5 exposure. The downregulated expression of miR-29b-2-5p, miR-193b-5p and miR-320c and upregulated expression of miR-100-5p, 125b-5p and unconservative_2_45093 in PM2.5 group were identified and reconfirmed by qRT-PCR. Chronic PM2.5 exposure causes bronchial epithelial cells atypical hyperplasia and induces EMT event in vivo, and it also induce the expression differences of miRNAs in exosome in vitro. Meanwhile, the identified differentially expressed exosome-miRNAs may partially associate with tumorigenesis. To sum up, the identified exosome-miRNAs may play role in the development of lung cancer induced by chronic PM2.5 exposure.
大量的流行病学研究表明,慢性 PM2.5 暴露与肺癌的发生有关,但目前尚不清楚其潜在机制。外泌体衍生的非编码 RNA,包括 miRNA,被认为在恶性疾病的发生和发展中发挥关键作用。因此,鉴定外泌体衍生的 miRNA 可以帮助我们更好地理解 PM2.5 诱导肺癌的分子毒性。如前所述,建立了 PM2.5 慢性暴露动物和细胞模型。通过 HE 染色评估体内肺组织的组织学改变。通过 Western blot 定量检测体内和体外 EMT 标志物的表达。然后提取细胞培养上清液中的外泌体,并提取和测序其中涉及的 miRNA。通过 RT-PCR 验证 miRNA 的不同表达水平。慢性 PM2.5 暴露诱导支气管上皮细胞非典型增生和大量巨噬细胞浸润。PM2.5 暴露在体内和体外诱导 EMT 事件,表现为波形蛋白表达增加和 E-钙黏蛋白表达减少。并且经过五轮 PM2.5 刺激后,体外细胞培养上清液中也释放出丰富的可提取的外泌体。通过测序,发现慢性 PM2.5 暴露组与对照组之间有 36 个 miRNA 存在差异表达,差异倍数大于 1.5 倍。其中,PM2.5 暴露后有 30 个外泌体 miRNA 上调,6 个下调。PM2.5 组 miR-29b-2-5p、miR-193b-5p 和 miR-320c 表达下调,miR-100-5p、125b-5p 和 unconservative_2_45093 表达上调,通过 qRT-PCR 进行了鉴定和再确认。慢性 PM2.5 暴露导致支气管上皮细胞非典型增生,并在体内诱导 EMT 事件,同时也导致体外外泌体中 miRNA 的表达差异。此外,鉴定出的差异表达外泌体-miRNA 可能与肿瘤发生部分相关。总之,鉴定出的外泌体-miRNA 可能在慢性 PM2.5 暴露诱导的肺癌发展中发挥作用。