Kidney Disease and Dialysis Center, Shaanxi Provincial People's Hospital, Xi'an, China.
J Biol Regul Homeost Agents. 2020;34(4):1369-1377. doi: 10.23812/20-280-A.
The aim of this study was to observe the expression of Klotho in renal tissues of mice with diabetic ne¬phropathy (DN), and to further explore the effect of Klotho on DN in mice and its mechanism. The 10-week-old mice in this experiment were divided into three groups: heterozygous db/+ mouse group (db/+ group, n=20), homozygous db/db mouse group (db/db group, n=20) and homozygous db/db mice + Klotho group (db/db + Klotho group, n=20). Firstly, Western blotting and immunohistochemical staining were applied to detect the protein expression of Klotho in the renal tissues of diabetic and non-diabetic mice of different ages. Finally, the protein expressions of fibroblast growth factor 2 (FGF2) and E-cadherin in the renal tissues of mice in each group were examined by Western blotting. The protein expression level of Klotho in the renal tissues of mice aged 10 and 16 weeks in the db/db group was remarkably lower than that in yhedb/+ group. In addition, it was found that db/db + Klotho group exhibited a prominently lower degree of interstitial fi¬brosis and content of Collagen I and Collagen III in the renal tissues than db/db group. Furthermore, it was revealed that the overexpression of Klotho could significantly repress the protein expression level of FGF2 but elevate that of E-cadherin in the renal tissues of DN mice. Klotho protein may ameliorate the renal injury and fibrosis in diabetic mice by inhibiting FGF2, so it is expected to become a targeted drug for DN.
本研究旨在观察 Klotho 在糖尿病肾病(DN)小鼠肾脏组织中的表达,并进一步探讨 Klotho 对小鼠 DN 的作用及其机制。实验中,将 10 周龄的小鼠分为三组:杂合子 db/+ 小鼠组(db/+ 组,n=20)、纯合子 db/db 小鼠组(db/db 组,n=20)和纯合子 db/db 小鼠+Klotho 组(db/db+Klotho 组,n=20)。首先,应用 Western blot 及免疫组化染色检测不同年龄糖尿病及非糖尿病小鼠肾脏组织中 Klotho 的蛋白表达情况。最后,应用 Western blot 检测各组小鼠肾脏组织中纤维母细胞生长因子 2(FGF2)和 E-钙黏蛋白的蛋白表达。结果显示,10 周龄和 16 周龄 db/db 组小鼠肾脏组织中 Klotho 蛋白表达水平显著低于 db/+ 组;db/db+Klotho 组小鼠肾脏组织中间质纤维化程度及胶原 I、胶原 III 含量均显著低于 db/db 组;此外,过表达 Klotho 可显著抑制 DN 小鼠肾脏组织中 FGF2 的蛋白表达水平,同时上调 E-钙黏蛋白的蛋白表达水平。Klotho 蛋白可能通过抑制 FGF2 改善糖尿病小鼠的肾脏损伤和纤维化,有望成为治疗 DN 的靶向药物。