Roeder Sebastian S, Stefanska Ania, Eng Diana G, Kaverina Natalya, Sunseri Maria W, McNicholas Bairbre A, Rabinovitch Peter, Engel Felix B, Daniel Christoph, Amann Kerstin, Lichtnekert Julia, Pippin Jeffrey W, Shankland Stuart J
Division of Nephrology, University of Washington, Seattle, Washington; Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
Division of Nephrology, University of Washington, Seattle, Washington;
Am J Physiol Renal Physiol. 2015 Jul 15;309(2):F164-78. doi: 10.1152/ajprenal.00144.2015. Epub 2015 May 27.
Kidney aging is accompanied by characteristic changes in the glomerulus, but little is known about the effect of aging on glomerular parietal epithelial cells (PECs), nor if the characteristic glomerular changes in humans and rats also occur in very old mice. Accordingly, a descriptive analysis was undertaken in 27-mo-old C57B6 mice, considered advanced age. PEC density was significantly lower in older mice compared with young mice (aged 3 mo), and the decrease was more pronounced in juxtamedullary glomeruli compared with outer cortical glomeruli. In addition to segmental and global glomerulosclerosis in older mice, staining for matrix proteins collagen type IV and heparan sulfate proteoglycan were markedly increased in Bowman's capsules of older mouse glomeruli, consistent with increased extracellular matrix production by PECs. De novo staining for CD44, a marker of activated and profibrotic PECs, was significantly increased in aged glomeruli. CD44 staining was more pronounced in the juxtamedullary region and colocalized with phosphorylated ERK. Additionally, a subset of aged PECs de novo expressed the epithelial-to-mesenchymal transition markers α-smooth muscle and vimentin, with no changes in epithelial-to-mesenchymal transition markers E-cadherin and β-catenin. The mural cell markers neural/glial antigen 2, PDGF receptor-β, and CD146 as well as Notch 3 were also substantially increased in aged PECs. These data show that mice can be used to better understand the aging kidney and that PECs undergo substantial changes, especially in juxtamedullary glomeruli, that may participate in the overall decline in glomerular structure and function with advancing age.
肾脏衰老伴随着肾小球的特征性变化,但关于衰老对肾小球壁层上皮细胞(PEC)的影响知之甚少,也不清楚人类和大鼠中观察到的肾小球特征性变化是否也会出现在非常老龄的小鼠中。因此,我们对27月龄的C57B6小鼠(已步入老龄)进行了描述性分析。与年轻小鼠(3月龄)相比,老龄小鼠的PEC密度显著降低,且与外皮质肾小球相比,近髓肾小球中的这种降低更为明显。除了老龄小鼠中的节段性和整体性肾小球硬化外,老龄小鼠肾小球鲍曼囊内IV型胶原蛋白和硫酸乙酰肝素蛋白聚糖等基质蛋白的染色显著增加,这与PEC产生细胞外基质增加一致。活化和促纤维化PEC的标志物CD44的新生染色在老龄肾小球中显著增加。CD44染色在近髓区域更为明显,并与磷酸化的细胞外信号调节激酶共定位。此外,一部分老龄PEC开始表达上皮-间充质转化标志物α-平滑肌肌动蛋白和波形蛋白,而上皮-间充质转化标志物E-钙黏蛋白和β-连环蛋白没有变化。壁细胞标志物神经/胶质抗原2、血小板衍生生长因子受体-β和CD146以及Notch 3在老龄PEC中也显著增加。这些数据表明,小鼠可用于更好地理解衰老肾脏,且PEC会发生实质性变化,尤其是在近髓肾小球中,这些变化可能参与了随着年龄增长肾小球结构和功能的整体衰退。