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Adipose tissue-derived stem cell treatment prevents renal disease progression

机译:脂肪组织来源的干细胞治疗可预防肾脏疾病的进展

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Adipose tissue-derived stem cells (ASCs) are an attractive source of stem cells with regenerative properties that are similar to those of bone marrow stem cells. Here, we analyze the role of ASCs in reducing the progression of kidney fibrosis. Progressive renal fibrosis was achieved by unilateral clamping of the renal pedicle in mice for 1 h; after that, the kidney was reperfused immediately. Four hours after the surgery, 2 × 10 5 ASCs were intraperitoneally administered, and mice were followed for 24 h posttreatment and then at some other time interval for the next 6 weeks. Also, animals were treated with 2 × 10 5 ASCs at 6 weeks after reperfusion and sacrificed 4 weeks later to study their effect when interstitial fibrosis is already present. At 24 h after reperfusion, ASCtreated animals showed reduced renal dysfunction and enhanced regenerative tubular processes. Renal mRNA expression of IL-6 and TNF was decreased in ASC-treated animals, whereas IL-4, IL-10, and HO-1 expression increased despite a lack of ASCs in the kidneys as determined by SRY analysis. As expected, untreated kidneys shrank at 6 weeks, whereas the kidneys of ASC-treated animals remained normal in size, showed less collagen deposition, and decreased staining for FSP-1, type I collagen, and Hypoxyprobe. The renal protection seen in ASC-treated animals was followed by reduced serum levels of TNF-α, KC, RANTES, and IL-1α. Surprisingly, treatment with ASCs at 6 weeks, when animals already showed installed fibrosis, demonstrated amelioration of functional parameters, with less tissue fibrosis observed and reduced mRNA expression of type I collagen and vimentin. ASC therapy can improve functional parameters and reduce progression of renal fibrosis at early and later times after injury, mostly due to early modulation of the inflammatory response and to less hypoxia, thereby reducing the epithelial-mesenchymal transition.
机译:脂肪组织干细胞(ASC)是具有与骨髓干细胞相似的再生特性的干细胞的诱人来源。在这里,我们分析了ASC在减少肾脏纤维化进程中的作用。通过单侧夹紧小鼠肾蒂1 h可达到进行性肾纤维化。之后,立即对肾脏进行再灌注。手术后四个小时,腹膜内注射2×10 5 ASC,对小鼠进行治疗后24小时,然后在接下来的6周内以其他时间间隔进行随访。同样,在再灌注后第6周用2×10 5 ASC处理动物,并在4周后处死动物以研究其间质纤维化已经存在的效果。在再灌注后24小时,ASC处理的动物表现出减少的肾功能障碍和增强的肾小管再生过程。通过SRY分析确定,尽管在肾脏中缺乏ASC,但在接受ASC治疗的动物中,肾脏IL-6和TNF的mRNA表达降低,而IL-4,IL-10和HO-1的表达增加。如预期的那样,未经治疗的肾脏在第6周萎缩,而经ASC治疗的动物的肾脏大小保持正常,胶原蛋白沉积减少,FSP-1,I型胶原蛋白和Hypoxyprobe的染色减少。在接受ASC治疗的动物中观察到的肾脏保护作用是血清TNF-α,KC,RANTES和IL-1α降低。出乎意料的是,当动物已经显示出已安装的纤维化时,在6周时用ASCs治疗表明功能参数得到改善,观察到的组织纤维化更少,I型胶原和波形蛋白的mRNA表达降低。 ASC治疗可改善损伤后早期和晚期的功能参数并减少肾纤维化的进展,这主要是由于炎症反应的早期调节和较少的缺氧,从而减少了上皮-间质转化。

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