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PM 诱导 k-ras 沉默的 HBE 细胞差异表达蛋白的蛋白质组学特征。

Proteomic characteristics of PM-induced differentially expressed proteins in k-ras-silenced HBE cells.

机构信息

School of Public Health, University of South China, Hengyang, China.

Shenzhen Center for Disease Control and Prevention, Institute of environment and health, Shenzhen, China.

出版信息

Toxicol Mech Methods. 2022 Jul;32(6):431-438. doi: 10.1080/15376516.2022.2028328. Epub 2022 Jan 19.

Abstract

The human bronchial epithelial cells (HBE) and K-ras-silenced HBE cells were treated with fine particulate matter (PM) samples from Taiyuan for 24 h. To screen the proteomic characteristics of PM-induced differentially expressed proteins (DEPs), the Q Exactive mass spectrometer was used. Gene ontology (GO) analysis, Kyoto encyclopedia of genes and genomes (KEGG) analysis, functional prediction, protein-protein interaction (PPI) network analysis, and visualization of differential protein interactions were performed. 251 DEPs in K-ras silenced cells and 535 DEPs in normal HBE cells were identified, respectively. KEGG analysis showed that the differentially expressed proteins of PM-treated cells were related to the biosynthesis of ribosomes, antibiotics, and amino acids. On the other hand, K-ras silenced cells were related to metabolic pathways, RNA transport, and DNA replication. Through the construction of a PPI network, the top 10 hub proteins were screened from the two cell groups, among which MRPL13, RPS20, and EIF1AX were of great significance. Our results indicated that the K-ras gene plays an important role in PM-induced DEPs, and the findings provide a scientific basis for the further study of PM toxic mechanisms and biomarkers.

摘要

将人类支气管上皮细胞(HBE)和 K-ras 沉默的 HBE 细胞用来自太原的细颗粒物(PM)样本处理 24 小时。为了筛选 PM 诱导的差异表达蛋白(DEPs)的蛋白质组学特征,使用了 Q Exactive 质谱仪。进行了基因本体论(GO)分析、京都基因与基因组百科全书(KEGG)分析、功能预测、蛋白质-蛋白质相互作用(PPI)网络分析以及差异蛋白相互作用的可视化。分别鉴定了 K-ras 沉默细胞中的 251 个 DEPs 和正常 HBE 细胞中的 535 个 DEPs。KEGG 分析表明,PM 处理细胞的差异表达蛋白与核糖体、抗生素和氨基酸的生物合成有关。另一方面,K-ras 沉默细胞与代谢途径、RNA 转运和 DNA 复制有关。通过构建 PPI 网络,从两个细胞群中筛选出前 10 个枢纽蛋白,其中 MRPL13、RPS20 和 EIF1AX 具有重要意义。我们的结果表明,K-ras 基因在 PM 诱导的 DEPs 中起重要作用,这些发现为进一步研究 PM 毒性机制和生物标志物提供了科学依据。

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