Nephrology Department, Guangzhou Women and Children's Medical Center, Guangzhou, 510000, China.
Pediatric Department, Gansu Province People's Hospital, Lanzhou City, 730000, China.
Biochem Biophys Res Commun. 2022 Mar 5;595:69-75. doi: 10.1016/j.bbrc.2022.01.061. Epub 2022 Jan 21.
The molecular mechanism of in hyperlipidemia-induced renal injury has not been elucidated. Angiogenin-like protein 4 (ANGPTL4) is a key regulator of lipid metabolism. The role of ANGPTL4 hyperlipidemia-induced renal injury has not been reported.
Wild type C57 mice and gene angptl4 knockout mice were fed with 60% high fat diet or normal diet respectively. The serum lipid, urinary albumin and renal pathology were tested at the 9th, 13th, 17th and 21st week with high fat diet.
Elevated blood lipids in the wild-type mice with high-fat diet were found at 9th week. At the 17th week, the level of urinary albumin in high-fat fed wild type mice were significantly higher than which with normal diet, correspondingly, segmental fusion of podocyte foot process in kidney could be observed in these hyperlipidemia mice. IHC showed that the expression of ANGPTL4 in glomeruli of high-fat fed wild type mice began significant elevated since the 9th week. When given high fat diet, compared to the wild type, the gene angptl4 knockout mice showed significantly alleviated the levels of hyperlipidemia, proteinuria and effacement of podocyte foot process. Finally, the expression of ACTN4 showed remarkably lower in glomeruli podocyte of wild type mice fed high fat diet than that of wild type mice with normal diet at each time-point (P < 0.01). Differently, the expression of ACTN4 in gene angptl4 knockout mice did not happen significantly weaken when given the same dose of high fat diet.
ANGPTL4 could play a role in hyperlipidemic-induced renal injury via down-regulating the expression of ACTN4 in kidney podocyte.
高脂血症诱导的肾损伤的分子机制尚未阐明。血管生成素样蛋白 4(ANGPTL4)是脂质代谢的关键调节因子。ANGPTL4 在高脂血症诱导的肾损伤中的作用尚未报道。
分别用普通饲料和 60%高脂饲料喂养野生型 C57 小鼠和基因 angptl4 敲除小鼠。在第 9、13、17 和 21 周用高脂饲料检测血清脂质、尿白蛋白和肾脏病理。
高脂喂养的野生型小鼠第 9 周即出现血脂升高。第 17 周时,高脂喂养野生型小鼠的尿白蛋白水平明显高于正常饮食组,相应地,这些高脂血症小鼠的肾小球足细胞足突融合。免疫组化显示,高脂喂养的野生型小鼠肾小球中 ANGPTL4 的表达从第 9 周开始明显升高。给予高脂饮食时,与野生型相比,基因 angptl4 敲除小鼠的高脂血症、蛋白尿和足细胞足突融合程度明显减轻。最后,高脂饮食喂养的野生型小鼠肾小球足细胞中 ACTN4 的表达明显低于正常饮食的野生型小鼠(P<0.01)。不同的是,在给予相同剂量的高脂饮食时,基因 angptl4 敲除小鼠中 ACTN4 的表达并没有明显减弱。
ANGPTL4 可能通过下调肾脏足细胞中 ACTN4 的表达在高脂血症诱导的肾损伤中发挥作用。