首页> 外文期刊>Peritoneal dialysis international: Journal of the International Society for Peritoneal Dialysis >Modulation of fibrinolytic system components in mesothelial cells by hyaluronan.
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Modulation of fibrinolytic system components in mesothelial cells by hyaluronan.

机译:透明质酸对间皮细胞中纤溶系统成分的调节。

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OBJECTIVE: Hyaluronan (HA) is an important extracellular matrix component and is involved in fluid homeostasis, tissue repair, and response to infections. Previous studies have shown that supplementation of dialysis fluid with high molecular weight HA may have a positive impact on peritoneal solute and fluid transport characteristics. In the present study, we investigated the impact of HA on the synthesis of tissue-type plasminogen activator (t-PA) and its inhibitor, plasminogen activator inhibitor type 1 (PAI-1) in cultured human peritoneal mesothelial cells (MC). METHODS: Cultured human peritoneal MC isolated from omental tissue were used for the experiments. Concentrations of t-PA and PAI-1 antigens were measured in conditioned media of confluent MC using ELISA. Northern blot analysis was performed to investigate mRNA expression of t-PA, PAI-1, and low-density lipoprotein receptor-related protein. RESULTS: Hyaluronan in a concentration as suggested for supplementation of dialysis fluid (10 mg/dL) did not have a significant impact on the synthesis of t-PA or PAI-1 in human MC. However, incubation of MC with higher concentrations of HA (30-1000 mg/dL) resulted in a concentration- and time- (8- 48 hours) dependent decrease in t-PA antigen release and mRNA expression. In contrast, PAI-1 antigen secretion was distinctly but not significantly increased in the presence of HA. CONCLUSION: The expression of t-PA and PAI-1 in MC was not affected by low concentrations of HA. Therefore, it is reasonable to assume that supplementation of dialysis fluid with HA (10 mg/dL) will not decrease mesothelial fibrinolytic activity. Only high concentrations (> 50 mg/dL) may disturb the balance between intraperitoneal generation and degradation of fibrin by decreasing t-PA synthesis.
机译:目的:透明质酸(HA)是重要的细胞外基质成分,参与液体体内稳态,组织修复和对感染的反应。先前的研究表明,补充高分子量HA的透析液可能会对腹膜溶质和液体的输送特性产生积极影响。在本研究中,我们研究了HA对培养的人腹膜间皮细胞(MC)中组织型纤溶酶原激活物(t-PA)及其抑制剂纤溶酶原激活物抑制剂1型(PAI-1)合成的影响。方法:从大网膜组织中分离培养的人腹膜MC。使用ELISA在融合MC的条件培养基中测量t-PA和PAI-1抗原的浓度。进行了Northern印迹分析以研究t-PA,PAI-1和低密度脂蛋白受体相关蛋白的mRNA表达。结果:透明质酸的建议浓度可补充透析液(10 mg / dL),对人MC中t-PA或PAI-1的合成没有显着影响。但是,将MC与较高浓度的HA(30-1000 mg / dL)孵育会导致t-PA抗原释放和mRNA表达的浓度和时间依赖性(8-48小时)减少。相反,在HA存在下,PAI-1抗原的分泌明显但没有明显增加。结论:低浓度的HA不影响MC中t-PA和PAI-1的表达。因此,可以合理地假设向透析液中补充HA(10 mg / dL)不会降低间皮纤维蛋白溶解活性。只有高浓度(> 50 mg / dL)才能通过减少t-PA合成来扰乱腹膜内生成与纤维蛋白降解之间的平衡。

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