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首页> 外文期刊>International journal of biological sciences >Diabetes Induced Changes in Podocyte Morphology and Gene Expression Evaluated Using GFP Transgenic Podocytes
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Diabetes Induced Changes in Podocyte Morphology and Gene Expression Evaluated Using GFP Transgenic Podocytes

机译:糖尿病诱导足细胞形态和基因表达的变化,使用GFP转基因足细胞进行评估

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摘要

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.
机译:尚未在分离的足细胞上检查体内糖尿病在糖尿病中的作用。为了实现这一点,GFP在PGFP转基因小鼠的足细胞中组成性表达,将其繁殖到OVE小鼠以产生糖尿病性OVE-GFP小鼠。查看GFP荧光,可见和可测量地消除了OVE-GFP足细胞的足突,这在轻度STZ糖尿病患者中没有发生。从每只PGFP小鼠中纯化了超过300,000足细胞,但是每位糖尿病OVE-GFP小鼠仅纯化了49,000足细胞。 OVE-GFP小鼠的低收率似乎是由于大多数OVE-GFP糖尿病足细胞的脆性状态所致,它们在分离过程中无法幸免。分离出的糖尿病足细胞具有高水平的脂质过氧化产物4-HNE,并且它们对因氧化应激而导致的死亡更敏感。 OVE-GFP足细胞的基因阵列分析显示,糖尿病对炎症相关基因的诱导作用强。四个CXC趋化因子被诱导至少3倍,并且首次证明OVE,dbdb和STZ糖尿病在足细胞中特异性诱导趋化因子CXCL1。

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