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Protection Mechanisms Of EPA On Renal Tubular Epithelial Cells Injury Stimulated By Albumin

Posted on:2015-03-29Degree:MasterType:Thesis
Country:ChinaCandidate:W C HanFull Text:PDF
GTID:2254330431454025Subject:Academy of Pediatrics
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BackgroundAmong various kinds of chronic kidney disease (CKD), renal fibrosis is the common pathological basis and the leading cause of end-stage renal disease. Pathological changes of the renal fibrosis include glomerulosclerosis and tubule-interstitial fibrosis. Damage to the renal tubular epithelial cells (HK-2) can cause the secretion of pro-inflammation cytokine, profibrogenic cytokines, and matrix protein. These inflammatory agents strengthen the injury to HK-2. This vicious circle is the major reason for renal fibrosis. Factors such as integrin linked kinase, integrin β1and peroxisome proliferator-activated receptor y (PPARy) have a very close relationship with renal fibrosis.N-3polyunsaturated fatty acid (n-3PUFA) is necessary in mammals. It mainly comes from the food, including eicosapentaenoic acid and docosahexaenoic acid. Fish oil is extracted from deep-sea fish, and is rich in n-3polyunsaturated fatty acids. Besides the anti-thrombotic effect, vasodilation, blood lipoid adjustment and anti-tumor effect, fish oil has a renal protective effect.In this study, we investigated the effects of EPA on the expression of PPARy, ILK and integrin (31in HK-2stimulated by albumin and to explore its possible protective mechanisms.MethodsThe HK-2of logarithmic growth phase was used. After serum-free cultured for24h, the cells were synchronized in the Go period, and then divided into four groups:the control group; human albumin group (model group, albumin20.0mg/L); Albumin plus EPA (10μmol/L,100μmol/L) group. All the cells were cultured in37℃,5%CO2for24h,48h and72h.The expression of PPARy, integrin β1and ILK was determined by Western Blotting; The mRNA expression of PPARy, integrin β1and ILK were eterminated by RT-PCR.Results1. Effects of EPA on the expression of PPARy in HK-2stimulated by albumin.Albumin could inhibit PPARy protein and mRNA expression; EPA could promote the albumin stimulation HK-2PPARy protein and mRNA expression.2. Effects of EPA on the expression of ILK in HK-2stimulated by albumin.Albumin could promote ILK protein and mRNA expression; EPA could inhibit the albumin stimulation HK-2ILK protein and mRNA expression.3. Effects of EPA on the expression of integrin β1in HK-2stimulated by albumin.Albumin could inhibit integrin β1protein and mRNA expression; EPA could promote the albumin stimulation HK-2integrin β1protein and mRNA expression.Conclusion1. EPA can promote albumin-induced HK-2PPARy protein and gene expression.2. EPA can reduce albumin-induced HK-2ILK protein and gene expression.3. EPA can promote albumin-induced HK-2integrin β1protein and gene expression.
Keywords/Search Tags:eicosapentaenoic acid, albumin, peroxisome proliferator activatedreceptors-γ, integrin, integrin-linked kinase
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