Ambrocio-Ortiz Enrique, Pérez-Rubio Gloria, Ramírez-Venegas Alejandra, Hernández-Zenteno Rafael, Del Angel-Pablo Alma D, Pérez-Rodríguez Martha E, Salazar Ana M, Abarca-Rojano Edgar, Falfán-Valencia Ramcés
HLA Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, Mexico.
Tobacco Smoking and COPD Research Department, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, Mexico.
Front Genet. 2020 Jan 9;10:1307. doi: 10.3389/fgene.2019.01307. eCollection 2019.
Heat shock proteins (HSP) genes are a superfamily responsible for encoding highly conserved proteins that are important for antigen presentation, immune response regulation, and cellular housekeeping processes. These proteins can be increased by cellular stress related to pollution, for example, smoke from biomass burning and/or tobacco smoking. Single nucleotide polymorphisms (SNPs) in these genes could affect the levels of their proteins, as well as the susceptibility to developing lung diseases, such as chronic obstructive pulmonary disease (COPD), related to the exposure to environmental factors. The subjects included were organized into two comparison groups: 1,103 smokers (COPD patients, COPD-S = 360; smokers without COPD, SWOC = 743) and 442 never-smokers who were chronically exposed to biomass smoke (COPD patients, COPD-BS = 244; exposed without COPD, BBES = 198). Eight SNPs in three genes were selected and genotyped: four in , two in , and two in . Sputum expectoration was induced to obtain pulmonary cells and relative quantification of mRNA expression. Subsequently, the intracellular protein levels of total Hsp27, phosphorylated Hsp27 (Hsp27p), Hsp60, and Hsp70 were measured in a sample of 148 individuals selected based on genotypes. In the smokers' group, by a dominant model analysis, we found associations between rs1008438 (CA+AA; p = 0.006, OR = 1.52), rs6457452 (CT+TT; p = 0.000015, OR = 1.99), and rs2763979 (CT+TT; p = 0.007, OR = 1.60) and the risk to COPD. Among those exposed to biomass-burning smoke, only rs1008438 (CA+AA; p < 0.01, OR = 2.84) was associated. Additionally, rs1008438 was associated with disease severity in the COPD-S group (AA; p = 0.02, OR = 2.09). An increase in the relative expression level of was found (12-fold change) in the COPD-BS over the BBES group. Differences in Hsp27 and Hsp60 proteins levels were found (p < 0.05) in the comparison of COPD-S vs. SWOC. Among biomass-burning smoke-exposed subjects, differences in the levels of all proteins (p < 0.05) were detected. SNPs in HSP genes are associated with the risk of COPD and severe forms of the disease. Differences in the intracellular Hsp levels are altered depending on the exposition source.
热休克蛋白(HSP)基因是一个超家族,负责编码高度保守的蛋白质,这些蛋白质对抗抗原呈递、免疫反应调节和细胞管家过程很重要。这些蛋白质可因与污染相关的细胞应激而增加,例如生物质燃烧和/或吸烟产生的烟雾。这些基因中的单核苷酸多态性(SNP)可能会影响其蛋白质水平,以及与接触环境因素相关的患肺部疾病(如慢性阻塞性肺疾病(COPD))的易感性。纳入的受试者被分为两个比较组:1103名吸烟者(COPD患者,COPD-S = 360;无COPD的吸烟者,SWOC = 743)和442名长期接触生物质烟雾的从不吸烟者(COPD患者,COPD-BS = 244;无COPD的接触者,BBES = 198)。选择并对三个基因中的八个SNP进行基因分型: 中的四个, 中的两个,以及 中的两个。诱导咳痰以获得肺细胞并对mRNA表达进行相对定量。随后,在根据基因型选择的148名个体的样本中测量了总Hsp27、磷酸化Hsp27(Hsp27p)、Hsp60和Hsp70的细胞内蛋白质水平。在吸烟者组中,通过显性模型分析,我们发现rs1008438(CA+AA;p = 0.006,OR = 1.52)、rs6457452(CT+TT;p = 0.000015,OR = 1.99)和rs2763979(CT+TT;p = 0.007,OR = 1.60)与患COPD的风险相关。在接触生物质燃烧烟雾的人群中,只有rs1008438(CA+AA;p < 0.01,OR = 2.84)与之相关。此外,rs1008438与COPD-S组的疾病严重程度相关(AA;p = 0.02,OR = 2.09)。发现COPD-BS组中 的相对表达水平增加(12倍变化),高于BBES组。在COPD-S与SWOC的比较中,发现Hsp27和Hsp60蛋白水平存在差异(p < 0.05)。在接触生物质燃烧烟雾的受试者中,检测到所有蛋白质水平存在差异(p < 0.05)。HSP基因中的SNP与COPD风险及其严重形式相关。细胞内Hsp水平的差异根据暴露源而改变。