Xu Jianxiang, Zheng Shirong, Kralik Patricia M, Krishnan Laxminarayanan, Huang Hui, Hoying James B, Cai Lu, Carlson Edward C, Tan Yi, Epstein Paul N
1. Department of Pediatrics, University of Louisville;
2. Cardiovascular Innovations Institute, University of Louisville;
Int J Biol Sci. 2016 Jan 1;12(2):210-8. doi: 10.7150/ijbs.13057. eCollection 2016.
The effect of diabetes in vivo has not been examined on isolated podocytes. To achieve this, GFP was expressed constitutively in podocytes of PGFP transgenic mice which were bred to OVE mice to produce diabetic OVE-GFP mice. Viewing GFP fluorescence, foot processes of OVE-GFP podocytes were visually and measurably effaced, which did not occur with less severe STZ diabetes. Over 300,000 podocytes were purified from each PGFP mouse but only 49,000 podocytes per diabetic OVE-GFP mouse. The low yield from OVE-GFP mice appeared to be due to more fragile state of most OVE-GFP diabetic podocytes which did not survive the isolation process. Diabetic podocytes that were isolated had high levels of the lipid peroxidation product 4-HNE and they were more sensitive to death due to oxidative stress. Gene array analysis of OVE-GFP podocytes showed strong diabetes induction of genes involved in inflammation. Four CXC chemokines were induced at least 3-fold and the chemokine CXCL1 was shown for the first time to be specifically induced in podocytes by OVE, dbdb and STZ diabetes.
糖尿病对体内分离的足细胞的影响尚未得到研究。为了实现这一点,在PGFP转基因小鼠的足细胞中组成性表达绿色荧光蛋白(GFP),将这些小鼠与OVE小鼠杂交以产生糖尿病OVE-GFP小鼠。观察GFP荧光发现,OVE-GFP足细胞的足突在视觉上和测量上均消失,而在病情较轻的链脲佐菌素诱导的糖尿病中并未出现这种情况。从每只PGFP小鼠中纯化出超过300,000个足细胞,但每只糖尿病OVE-GFP小鼠仅得到49,000个足细胞。OVE-GFP小鼠足细胞产量低似乎是由于大多数OVE-GFP糖尿病足细胞状态更脆弱,在分离过程中无法存活。分离出的糖尿病足细胞中脂质过氧化产物4-羟基壬烯醛(4-HNE)水平较高,并且它们对氧化应激导致的死亡更敏感。对OVE-GFP足细胞的基因芯片分析显示,糖尿病强烈诱导了与炎症相关的基因。四种CXC趋化因子的诱导倍数至少为3倍,趋化因子CXCL1首次被证明在OVE、db/db和链脲佐菌素诱导的糖尿病模型的足细胞中特异性诱导表达。