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Neutrophil gelatinase-associated lipocalin (NGAL) and matrix metalloproteinases as novel stress markers in children and young adults on chronic dialysis

机译:中性粒细胞明胶酶相关脂钙蛋白(NGAL)和基质金属蛋白酶作为慢性透析儿童和年轻人的新型应激指标

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Phenomena related to chronic kidney disease, such as atherosclerosis, aggravate with the introduction of dialysis. Matrix metalloproteinases (MMP) and factors modifying their activity, such as their tissue inhibitors (TIMP) or neutrophil gelatinase-associated lipocalin (NGAL), take part in the matrix turnover and the endothelial damage characteristic for atherogenesis. However, there are no data on the associations between these parameters and other known pro-atherogenic factors, or on the impact of various dialysis modalities on them. The aim of our study was to assess the serum concentrations of NGAL, MMP-7, MMP-9, and TIMP-1, as well as their correlations with human heat shock proteins (Hsp90α, anti-Hsp60), endothelial dysfunction (sE-selectin), and inflammation (hsCRP) in pediatric patients chronically dialyzed. Twenty-two children on automated peritoneal dialysis (APD), 17 patients on hemodialysis (HD) and 24 controls were examined. The serum concentrations of NGAL, MMP-7, MMP-9, TIMP-1, Hsp90α, anti-Hsp60, and sE-selectin were assessed by enzyme-linked immunosorbent assay (ELISA). The median values of NGAL, MMP-7, MMP-9, TIMP-1, and MMP-9/NGAL ratio were significantly elevated in all dialyzed children vs. controls and were higher in HD than in APD. The values of MMP-9/TIMP-1 and MMP-7/TIMP-1 ratios in the HD subjects were lower than those in the APD children. Hsp90α and anti-Hsp60 predicted the values of NGAL, MMPs, and TIMP-1. Additionally, sE-selectin was a predictor of NGAL levels, whereas NGAL predicted the MMP and TIMP-1 concentrations. The increased concentrations of examined parameters indicate the dysfunction of MMP/TIMP/NGAL system in the dialyzed children, more pronounced on hemodialysis. The discrepancies between dialysis modalities and correlations with heat shock proteins (HSPs) suggest that NGAL may be considered a novel stress protein, whereas MMP-7, MMP-9, and TIMP-1 may be regarded as indicators of stress response in the pediatric population on chronic dialysis.
机译:随着透析的引入,与慢性肾脏疾病如动脉粥样硬化有关的现象加剧。基质金属蛋白酶(MMP)及其修饰其活性的因子,例如其组织抑制剂(TIMP)或与中性粒细胞明胶酶相关的lipocalin(NGAL),均参与基质转换和动脉粥样硬化的内皮损伤特征。但是,没有关于这些参数与其他已知的促动脉粥样硬化因素之间的关联的数据,也没有关于各种透析方式对其的影响的数据。我们研究的目的是评估NGAL,MMP-7,MMP-9和TIMP-1的血清浓度,以及它们与人热休克蛋白(Hsp90α,抗Hsp60),内皮功能障碍(sE-选择素)和炎症(hsCRP)在小儿患者中进行了长期透析。检查了22例接受自动腹膜透析(APD)的儿童,17例接受血液透析(HD)的患者和24例对照。通过酶联免疫吸附测定(ELISA)评估NGAL,MMP-7,MMP-9,TIMP-1,Hsp90α,抗Hsp60和sE-选择素的血清浓度。与对照组相比,所有透析儿童的NGAL,MMP-7,MMP-9,TIMP-1和MMP-9 / NGAL的中位数值均显着升高,而HD高于APD。 HD受试者中MMP-9 / TIMP-1和MMP-7 / TIMP-1的值低于APD儿童。 Hsp90α和抗Hsp60预测NGAL,MMP和TIMP-1的值。另外,sE-选择蛋白是NGAL水平的预测因子,而NGAL预测MMP和TIMP-1浓度。所检查参数的浓度增加表明在透析儿童中MMP / TIMP / NGAL系统功能异常,在血液透析中更为明显。透析方式与热休克蛋白(HSP)相关性之间的差异表明,NGAL可能被认为是一种新型应激蛋白,而MMP-7,MMP-9和TIMP-1可能被视为儿科人群应激反应的指标进行慢性透析。

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