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间充质干细胞可预防实验性进行性肾衰竭,但会异常分化为肾小球脂肪细胞。

Mesenchymal stem cells prevent progressive experimental renal failure but maldifferentiate into glomerular adipocytes.

作者信息

Kunter Uta, Rong Song, Boor Peter, Eitner Frank, Müller-Newen Gerhard, Djuric Zivka, van Roeyen Claudia R, Konieczny Andrzej, Ostendorf Tammo, Villa Luigi, Milovanceva-Popovska Maja, Kerjaschki Dontscho, Floege Jürgen

机构信息

Division of Nephrology, University Hospital RWTH Aachen, Pauwelsstrasse 30, D-52057 Aachen, Germany.

出版信息

J Am Soc Nephrol. 2007 Jun;18(6):1754-64. doi: 10.1681/ASN.2007010044. Epub 2007 Apr 25.

Abstract

Glomerulonephritis (GN) is a major cause of renal failure. This study sought to determine whether intrarenal injection of rat mesenchymal stem cells (MSC) can preserve renal function in a progressive rat model of GN. Early in GN (day 10), fluorescently labeled rat MSC localized to more than 70% of glomeruli, ameliorated acute renal failure, and reduced glomerular adhesions. Fifty days later, proteinuria had progressed in controls to 40 +/- 25 mg/d but stayed low in MSC-treated rats (13 +/- 4 mg/d; P < 0.01). Renal function on day 60 in the MSC group was better than in medium controls. Kidneys of the MSC group as compared with controls on day 60 contained 11% more glomeruli per 1-mm(2) section of cortex but also significantly more collagen types I, III, and IV and alpha-smooth muscle actin. Approximately 20% of the glomeruli of MSC-treated rats contained single or clusters of large adipocytes with pronounced surrounding fibrosis. Adipocytes exhibited fluorescence in their cytoplasm and/or intracellular lipid droplets. Lipid composition in these adipocytes in vivo mirrored that of MSC that underwent adipogenic differentiation in vitro. Thus, in this GN model, the early beneficial effect of MSC of preserving damaged glomeruli and maintaining renal function was offset by a long-term partial maldifferentiation of intraglomerular MSC into adipocytes accompanied by glomerular sclerosis. These data suggest that MSC treatment can be a valuable therapeutic approach only if adipogenic maldifferentiation is prevented.

摘要

肾小球肾炎(GN)是肾衰竭的主要原因。本研究旨在确定肾内注射大鼠间充质干细胞(MSC)是否能在进行性大鼠GN模型中保留肾功能。在GN早期(第10天),荧光标记的大鼠MSC定位于超过70%的肾小球,改善急性肾衰竭,并减少肾小球粘连。50天后,对照组的蛋白尿进展至40±25mg/d,但在MSC治疗的大鼠中保持较低水平(13±4mg/d;P<0.01)。MSC组第60天的肾功能优于培养基对照组。与第60天的对照组相比,MSC组肾脏每1mm²皮质切片中的肾小球多11%,但I型、III型和IV型胶原蛋白以及α平滑肌肌动蛋白也明显更多。接受MSC治疗的大鼠中约20%的肾小球含有单个或成簇的大脂肪细胞,周围有明显的纤维化。脂肪细胞在其细胞质和/或细胞内脂滴中显示荧光。这些体内脂肪细胞中的脂质组成反映了体外经历脂肪生成分化的MSC的脂质组成。因此,在这个GN模型中,MSC早期保护受损肾小球和维持肾功能的有益作用被肾小球内MSC长期部分异常分化为脂肪细胞并伴有肾小球硬化所抵消。这些数据表明,只有防止脂肪生成异常分化,MSC治疗才可能是一种有价值的治疗方法。

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