Gao Lei, Juan Juan, Zheng Zimeng, Huang Lihua
Department of Public Health, International College, Krirk University, Bangkok 10220, Thailand.
School of Public Health, Baotou Medical College, Baotou 014030, China.
Toxics. 2024 Dec 18;12(12):917. doi: 10.3390/toxics12120917.
Nanoparticles of neodymium oxide (NPs-NdO) can induce respiratory-related diseases, including lung tissue injury when entering the organism through the respiratory tract. However, it is currently unclear whether they can induce epithelial-mesenchymal transition (EMT) in lung tissue and the related mechanisms. In this study, we investigated the function of circ_009773 in the process of EMT induced by NPs-NdO in lung tissue from in vivo as well as in vitro experiments. The findings showed that NPs-NdO induced EMT in 16HBE cells and SD rat lung tissues. This was characterised by a decrease in epithelial markers and an increase in mesenchymal markers. Additionally, circ_009773 expression was found to decrease in 16HBE cells infected with NPs-NdO and also decreased in the lung tissues of SD rats. Relevant experiments showed that circ_009773 inhibited EMT in NPs-NdO-treated 16HBE cells and SD rat lung tissues. The previous experiments revealed that circ_009773 was localised in the cytoplasm and functioned at the post-transcriptional level. With the EMT-related pathway used as the basis for circ_009773-related competing endogenous (ce)RNA mechanisms, our observations indicate that circ_009773 is capable of binding to and regulating the expression of miR-135b-5p. In summary, we found that circ_009773 inhibits the EMT induced by NPs-NdO in lung tissues, and this process likely occurs through competitive binding to miR-135b-5p.
氧化钕纳米颗粒(NPs-NdO)可诱发与呼吸相关的疾病,当通过呼吸道进入机体时,会导致肺组织损伤。然而,目前尚不清楚它们是否能诱导肺组织上皮-间质转化(EMT)及其相关机制。在本研究中,我们通过体内和体外实验,研究了circ_009773在NPs-NdO诱导的肺组织EMT过程中的作用。研究结果表明,NPs-NdO可诱导16HBE细胞和SD大鼠肺组织发生EMT。其特征是上皮标志物减少,间质标志物增加。此外,发现感染NPs-NdO的16HBE细胞中circ_009773表达降低,SD大鼠肺组织中也降低。相关实验表明,circ_009773可抑制NPs-NdO处理的16HBE细胞和SD大鼠肺组织中的EMT。先前实验表明,circ_009773定位于细胞质,在转录后水平发挥作用。以EMT相关通路为基础探讨circ_009773相关竞争性内源(ce)RNA机制,我们的观察结果表明,circ_009773能够结合并调节miR-135b-5p的表达。总之,我们发现circ_009773可抑制NPs-NdO诱导的肺组织EMT,这一过程可能通过与miR-135b-5p竞争性结合而发生。