Jung Ki-Yoon, Dean Dana, Jiang Jing, Gaylor Susan, Griffith William H, Burghardt Robert C, Parrish Alan R
Department of Medical Pharmacology and Toxicology, College of Medicine, Texas A&M University System Health Science Center, College Station, TX 77843-1114, USA.
Mech Ageing Dev. 2004 Jun;125(6):445-53. doi: 10.1016/j.mad.2004.04.001.
Aging is associated with a loss of renal reserve, and increased sensitivity to either xenobiotic or physiologic insult. Given the critical role of the cadherin/catenin complex in establishing and maintaining the integrity and polarity of tubular epithelial cells, it was hypothesized that aging was associated with alterations in renal cadherin/catenin complexes. Histological assessment of aged (24 months) kidneys harvested from male Fischer 344 rats demonstrates mild degeneration of proximal tubules, multifocal chronic lymphocytic infiltration, moderate development of protein casts inside tubules, and tubular dilatation or degeneration. Western blot analysis revealed that N-cadherin protein expression is not constant over 24 months. N-cadherin expression increased from 4 to 9 months, with peak levels at 9 and 13 months. A decrease in expression was seen at 19 months and an almost complete loss of expression was seen at 24 months. In contrast, the expression of E- and Ksp-cadherin was constant over 24 months. A loss of alpha-catenin at was seen at 19 and 24 months in the absence of changes in beta-, gamma-, and p120-catenin. This pattern of N-cadherin expression (increase followed by decrease) was confirmed by real-time PCR analysis, which demonstrated a similar pattern as the Western blot, suggesting that the loss of N-cadherin protein was due to decreased gene expression. The loss of N-cadherin was specific for the kidney, as no changes in N-cadherin expression in the liver, brain, or testes were seen during aging. The conclusion that loss of N-cadherin expression is a critical component of the renal dysfunction associated with aging is supported by the finding that caloric restriction attenuates the loss of N-cadherin, as well as the finding that a significant loss of N-cadherin is seen in the kidneys of ZDF x SHHF rats, a genetic model of end-stage renal disease. Cadherin and catenin expression was further analyzed by immunofluorescence. A significant loss of staining of both N-cadherin and alpha-catenin was seen in the proximal tubules of rats at 24 months. Interestingly, this corresponded with delocalization of the alpha-1 subunit of the Na+K+-ATPase, i.e. aberrant staining on cell-cell borders and some indication of apical staining in proximal tubules. Taken together, these data suggest that aging is associated with decreased expression of N-cadherin and alpha-catenin and is associated with a loss of cell polarity.
衰老与肾储备的丧失以及对外源性或生理性损伤的敏感性增加有关。鉴于钙黏蛋白/连环蛋白复合物在建立和维持肾小管上皮细胞的完整性和极性方面的关键作用,有人推测衰老与肾钙黏蛋白/连环蛋白复合物的改变有关。对从雄性Fischer 344大鼠获取的24月龄老龄肾脏进行组织学评估,结果显示近端小管轻度变性、多灶性慢性淋巴细胞浸润、小管内蛋白管型中度形成以及小管扩张或变性。蛋白质印迹分析显示,N -钙黏蛋白的蛋白表达在24个月内并非恒定不变。N -钙黏蛋白表达从4个月到9个月增加,在9个月和13个月时达到峰值水平。在19个月时表达下降,在24个月时几乎完全丧失表达。相比之下,E -钙黏蛋白和Ksp -钙黏蛋白的表达在24个月内保持恒定。在19个月和24个月时观察到α -连环蛋白缺失,而β -连环蛋白、γ -连环蛋白和p120 -连环蛋白没有变化。实时PCR分析证实了N -钙黏蛋白这种表达模式(先增加后减少),其显示出与蛋白质印迹相似的模式,表明N -钙黏蛋白蛋白的丧失是由于基因表达降低所致。N -钙黏蛋白的丧失在肾脏中具有特异性,因为在衰老过程中肝脏、大脑或睾丸中的N -钙黏蛋白表达未见变化。热量限制可减轻N -钙黏蛋白的丧失这一发现,以及在终末期肾病的遗传模型ZDF x SHHF大鼠的肾脏中观察到N -钙黏蛋白显著丧失这一发现,均支持N -钙黏蛋白表达丧失是与衰老相关的肾功能障碍的关键组成部分这一结论。通过免疫荧光进一步分析了钙黏蛋白和连环蛋白的表达。在24月龄大鼠的近端小管中观察到N -钙黏蛋白和α -连环蛋白的染色均显著丧失。有趣的是,这与Na⁺K⁺ - ATP酶α - 1亚基的定位异常相对应,即在细胞 - 细胞边界出现异常染色以及近端小管中有一些顶端染色的迹象。综上所述,这些数据表明衰老与N -钙黏蛋白和α -连环蛋白的表达降低有关,并与细胞极性丧失有关。