首页> 美国卫生研究院文献>Brazilian Journal of Medical and Biological Research >Proteomic data show an increase in autoantibodies andalpha-fetoprotein and a decrease in apolipoprotein A-II with time in sera fromsenescence-accelerated mice
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Proteomic data show an increase in autoantibodies andalpha-fetoprotein and a decrease in apolipoprotein A-II with time in sera fromsenescence-accelerated mice

机译:蛋白质组学数据显示自身抗体和甲胎蛋白和血清载脂蛋白A-II随时间的降低衰老加速小鼠

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摘要

We evaluated changes in levels by comparing serum proteins in senescence-accelerated mouse-prone 8 (SAMP8) mice at 2, 6, 12, and 15 months of age (SAMP8-2 m, -6 m, -12 m, -15 m) to age-matched SAM-resistant 1 (SAMR1) mice. Mice were sacrificed, and blood was analyzed by 2-dimensional electrophoresis combined with mass spectrometry. Five protein spots were present in all SAMP8 serum samples, but only appeared in SAMR1 samples at 15 months of age except for spot 3, which also showed a slight expression in SAMR1-12 m sera. Two proteins decreased in the sera from SAMP8-2 m, -6 m, and -12 m mice, and divided into 2 spots each in SAMP8-15 m sera. Thus, the total number of altered spots in SAMP8 sera was 7; of these, 4 were identified as Ig kappa chain V region (M-T413), chain A of an activity suppressing Fab fragment to cytochrome P450 aromatase (32C2_A), alpha-fetoprotein, and apolipoprotein A-II. M-T413 is a monoclonal CD4 antibody, which inhibits T cell proliferation. We found that M-T413 RNA level was significantly enhanced in splenocytes from SAMP8-2 m mice. This agreed with serum M-T413 protein alterations and a strikingly lower blood CD4+ T cell count in SAMP8 mice when compared to theage-matched SAMR1 mice, with the latter negatively correlating with serum M-T413protein volume. Age-related changes in serum proteins favored an increase inautoantibodies and alpha-fetoprotein and a decrease of apolipoprotein A-II,which occurred in SAMP8 mice at 2 months of age and onwards. These proteins mayserve as candidate biomarkers for early aging.
机译:我们通过比较2、6、12和15个月大的衰老加速易鼠8(SAMP8)小鼠中的血清蛋白(SAMP8-2 m,-6 m,-12 m,-15 m )至年龄相符的SAM抗性1(SAMR1)小鼠。处死小鼠,并通过二维电泳结合质谱分析血液。所有SAMP8血清样品中均存在5个蛋白斑点,但仅在15个月大的SAMR1样品中出现,斑点3除外,后者在SAMR1-12 m血清中也有少量表达。 SAMP8-2 m,-6 m和-12 m小鼠的血清中有两种蛋白质减少,而在SAMP8-15 m血清中每个蛋白质分成两个斑点。因此,SAMP8血清中斑点的总数为7;其中,有4个被鉴定为Igκ链V区(M-T413),抑制细胞色素P450芳香化酶(32C2_A)的Fab片段的活性链A,甲胎蛋白和载脂蛋白A-II。 M-T413是单克隆CD4抗体,可抑制T细胞增殖。我们发现SAMP8-2 m小鼠的脾细胞中M-T413 RNA水平显着提高。与SAMP8小鼠相比,这与SAMP8小鼠的血清M-T413蛋白改变和血液CD4 + T细胞计数显着降低相符。年龄匹配的SAMR1小鼠,后者与血清M-T413负相关蛋白质量。与年龄有关的血清蛋白变化有利于血清蛋白的增加自身抗体和甲胎蛋白以及载脂蛋白A-II减少,发生在2个月及以上的SAMP8小鼠中。这些蛋白质可能作为早期衰老的候选生物标志物。

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