Rotondo John Charles, Oton-Gonzalez Lucia, Selvatici Rita, Rizzo Paola, Pavasini Rita, Campo Gianluca Calogero, Lanzillotti Carmen, Mazziotta Chiara, De Mattei Monica, Tognon Mauro, Martini Fernanda
Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
Department of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Front Cell Dev Biol. 2020 Sep 3;8:550543. doi: 10.3389/fcell.2020.550543. eCollection 2020.
SERine Protein INhibitor-A1 (SERPINA1) is an inducible blood cell gene coding for alpha1-antitrypsin (AAT), a plasma protease inhibitor whose circulating levels are raised during inflammation, infection and advanced pregnancy. DNA methylation has been suggested to play a role in SERPINA1 gene expression regulation in peripheral blood mononuclear cells (PBMCs). The methylation status of in PBMCs is unknown. The aim of this study was to evaluate the methylation profile of the SERPINA1 promoter in PBMC. To this purpose PBMCs and serum were collected from healthy subjects (HS) ( = 75), including blood donors (BD) ( = 25), pregnant women at early pregnancy (EP) ( = 25), i.e., within the first trimester, and pregnant women at late pregnancy (LP) ( = 25), i.e., at the third trimester. DNA from PBMCs was treated with sodium bisulfite and PCR amplified for SERPINA1 gene promoter, followed by sequencing analyses. AAT serum levels were determined by ELISA test. was found hypermethylated in 58.7% of HS. The prevalence of hypermethylation was significantly higher in BD (68%) and EP (88%) than in LP (20%) ( < 0.01). The median serum AAT concentration was 1.07, 0.63, and 3.15 mg/ml in BD, EP, and LP, respectively ( < 0.05, BD and EP vs LP). This study indicates, for the first time, that SERPINA1 gene promoter is differentially methylated in PBMCs from HS. Likely, modulation of the methylation may be a novel epigenetic regulator mechanism of AAT expression in the PBMC of HS. Therefore, SERPINA1 gene promoter methylation may represent an epigenetic biomarker of PBMCs in healthy subjects.
丝氨酸蛋白酶抑制剂A1(SERPINA1)是一种可诱导的血细胞基因,编码α1 -抗胰蛋白酶(AAT),AAT是一种血浆蛋白酶抑制剂,其循环水平在炎症、感染和晚期妊娠期间会升高。已有研究表明DNA甲基化在外周血单核细胞(PBMC)的SERPINA1基因表达调控中发挥作用。PBMC中该基因的甲基化状态尚不清楚。本研究的目的是评估PBMC中SERPINA1启动子的甲基化谱。为此,从健康受试者(HS)(n = 75)中收集PBMC和血清,其中包括献血者(BD)(n = 25)、早孕(EP)(n = 25)即妊娠早期的孕妇以及晚孕(LP)(n = 25)即妊娠晚期的孕妇。PBMC的DNA用亚硫酸氢钠处理后,对SERPINA1基因启动子进行PCR扩增,随后进行测序分析。通过ELISA试验测定AAT血清水平。发现HS中有58.7%的样本该基因高度甲基化。BD(68%)和EP(88%)中该基因高度甲基化的发生率显著高于LP(20%)(P < 0.01)。BD、EP和LP的血清AAT浓度中位数分别为1.07、0.63和3.15 mg/ml(P < 0.05,BD和EP与LP相比)。本研究首次表明,HS的PBMC中SERPINA1基因启动子存在差异甲基化。甲基化的调节可能是HS的PBMC中AAT表达的一种新的表观遗传调控机制。因此,SERPINA1基因启动子甲基化可能代表健康受试者PBMC的一种表观遗传生物标志物。