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作 者:王哲[1] 刘晓玉[2] 张殿宝[2] 王秋实[1]
机构地区:[1]中国医科大学盛京医院输血科,辽宁沈阳110004 [2]中国医科大学细胞生物学卫生部重点实验室、干细胞与再生医学研究室,辽宁沈阳110001
出 处:《中国病理生理杂志》2014年第5期897-901,共5页Chinese Journal of Pathophysiology
基 金:辽宁省科技厅项目(No.2011225020;No.2012225014;No.2013225303)
摘 要:目的:探讨晚期糖基化终产物(AGEs)对人脂肪来源的间充质干细胞(hADSCs)促进创伤修复功能的影响。方法:体外培养hADSCs,实验分为牛血清白蛋白(BSA)对照组、低浓度糖基化修饰的牛血清白蛋白(AGE-BSA)效应组和高浓度AGE-BSA效应组。采用WST法和Transwell迁移实验检测各组细胞增殖和迁移情况。应用实时定量PCR和ELISA检测各组细胞分泌血管内皮生长因子(VEGF)、肝细胞生长因子(HGF)和胰岛素样生长因子1(IGF-1)的表达。结果:与对照组相比,AGE-BSA组增殖能力和迁移能力明显下降(P<0.05),VEGF、HGF和IGF-1 mRNA及蛋白表达水平显著降低(P<0.05)。结论:AGEs能损伤hADSCs的促进创伤修复功能,因而能够影响hADSCs治疗糖尿病皮肤溃疡病的治疗效果。AIM: To explore the effect of advanced glycosylatinn end products (AGEs) on the function of human adipose-derived stem cells (hADSCs) in promoting wound healing. METHODS: hADSCs were isolated by conventional method in vitro anti divided into control bovine serum albumin ( BSA ) group, low-dose AGE-BSA group anti highdose AGE-BSA group. The proliferatiun and migration of hADSCs with different treatments were determined by WST-8 assay and Transwell assay, respectively. In addition, the expression of vascular endothelial growth factor (VEGF) , hepatoeyte grnwth factor ( HGF), and insulin-like growth factor-1 ( IGF-1 ) at mRNA and protein levels was determined by realtime PCR and ELISA analysis. RESULTS: Compared with control group, the proliferation and migration abilities were significantly inhibited in the hADSCs of AGE-BSA group. The mRNA expression of VEGF, HGF and IGF-1 in AGE-BSA group was obviously lower than that in control group. The contents of VEGF, HGF and IGF-1 in hADSCs-c.onditioned medium in AGE-BSA group were also obviously lower than those in control group. CONCLUSION: AGEs alter the intrinsic properties of hADSCs and impair their functions in promoting wound healing, thus affecting the therapeutic potential of hADSCs in the treatment of diabetic ulcers.
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