Department of Microbiology and Clinical Immunology, The Children's Memorial Health Institute, Warsaw, Poland.
Collegium Medicum Nicolaus Copernicus University, Bydgoszcz, Poland.
Mediators Inflamm. 2020 Sep 10;2020:8327945. doi: 10.1155/2020/8327945. eCollection 2020.
Gene expression profiles of matrix metalloproteinases () and their tissue inhibitors () were evaluated in peripheral blood leukocytes of children with nonalcoholic fatty liver disease (NAFLD). Gene expression patterns were correlated with their plasma protein counterparts, systemic parameters of liver injury, and selected markers of inflammation. The -, -, -, -, -, -, -, and - transcripts levels were tested by the real-time PCR. Plasma concentrations of MMP-9, TIMP-1, MMP-9/TIMP-1 ratio, MMP-2/TIMP-2 ratio, sCD14, leptin, resistin, IL-1 beta, and IL-6 and serum markers of liver injury were estimated by ELISA. The -, - expression levels, plasma amounts of MMP-9, TIMP-1, and the MMP-9/TIMP-1 ratio were increased in children with NAFLD. Concentrations of AST, ALT, GGT, and leptin were elevated in serum patients with NAFLD, while concentration of other inflammatory or liver injury markers was unchanged. The - and - levels correlated with serum liver injury parameters (ALT and GGT concentrations, respectively); there were no other correlations between gene expression profiles, their plasma counterparts, and serum inflammatory markers. Association of - and -9 expression with serum liver injury parameters (ALT, GGT) may suggest leukocyte engagement in the early stages of NAFLD development which possibly precedes subsequent systemic inflammatory responses.
我们评估了非酒精性脂肪性肝病 (NAFLD) 患儿外周血白细胞中基质金属蛋白酶 () 和其组织抑制剂 () 的基因表达谱。基因表达模式与它们的血浆蛋白对应物、肝损伤的系统参数和选定的炎症标志物相关联。通过实时 PCR 检测 -、-、-、-、-、-、- 和 - 转录本水平。通过 ELISA 测定 MMP-9、TIMP-1、MMP-9/TIMP-1 比值、MMP-2/TIMP-2 比值、sCD14、瘦素、抵抗素、IL-1β 和 IL-6 的血浆浓度和血清肝损伤标志物。NAFLD 患儿的 - 和 - 表达水平、血浆 MMP-9、TIMP-1 量和 MMP-9/TIMP-1 比值增加。血清中 NAFLD 患者的 AST、ALT、GGT 和瘦素浓度升高,而其他炎症或肝损伤标志物的浓度不变。- 和 - 水平与血清肝损伤参数(ALT 和 GGT 浓度)相关;基因表达谱、其血浆对应物和血清炎症标志物之间没有其他相关性。- 和 -9 表达与血清肝损伤参数(ALT、GGT)的关联可能表明白细胞参与了 NAFLD 发展的早期阶段,这可能先于随后的全身炎症反应。