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DNA sequence variation in the promoter region of the VEGF gene: Impacts on VEGF gene expression and maximal oxygen consumption.

机译:VEGF基因启动子区域中的DNA序列变异:对VEGF基因表达和最大耗氧量的影响。

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Maximal oxygen consumption (Vo2max) is inversely associated with cardiovascular and all-cause mortality and is responsive to aerobic exercise training. A portion of the increase in Vo2max with aerobic exercise training can be attributed to an increase in skeletal muscle capillarity (i.e., angiogenesis), which contributes to increased blood flow and oxygen extraction in working skeletal muscle. One contributing factor to exercise-induced angiogenesis is vascular endothelial growth factor (VEGF), as it is an endothelial cell proliferation and migration factor that is upregulated by acute aerobic exercise. Significant variability has been observed in VEGF protein levels, VEGF gene expression, skeletal muscle capillarity, and Vo2max before and after aerobic exercise training. Additionally, variability is found in the DNA sequence of the gene encoding VEGF. Variation in the VEGF gene has the ability to impact VEGF gene expression and VEGF protein level and because of the relationship between VEGF, angiogenesis, and Vo2max, we hypothesized that variation in the VEGF gene is related to VEGF gene expression in human myoblasts, plasma VEGF level, and Vo2max before and after aerobic exercise training.; The present report shows that VEGF promoter region haplotype impacts VEGF gene expression in human myoblasts in vitro. It was also found that VEGF promoter region haplotype was associated with Vo2max in older men and women before and after exercise training in a manner that is consistent with the results of the VEGF gene expression experiments. Additionally, we found that plasma VEGF level was not associated with VEGF promoter region haplotype, nor did plasma VEGF level correlate with baseline Vo2max or DeltaVo2max with aerobic exercise training. To date, we are the first to report that VEGF promoter region haplotype impacts VEGF gene expression in human myoblasts and is associated with Vo2max. These results have potential implications for aerobic exercise training and may also contribute to the understanding of the function of the VEGF promoter region in different cell types. Furthermore, these results may prove relevant in the study of pathological conditions which can be affected by angiogenesis, namely obesity, cancer, coronary artery disease, and peripheral artery disease.
机译:最大耗氧量(Vo2max)与心血管疾病和全因死亡率成反比,对有氧运动训练有反应。有氧运动训练中最大Vo2max的增加的一部分可以归因于骨骼肌毛细血管的增加(即血管生成),这有助于增加工作骨骼肌的血流量和氧气提取量。运动诱导的血管生成的一个促成因素是血管内皮生长因子(VEGF),因为它是被有氧运动上调的内皮细胞增殖和迁移因子。在有氧运动训练前后,VEGF蛋白水平,VEGF基因表达,骨骼肌毛细血管和Vo2max均存在显着差异。另外,在编码VEGF的基因的DNA序列中发现了变异性。 VEGF基因的变异具有影响VEGF基因表达和VEGF蛋白水平的能力,并且由于VEGF,血管生成和Vo2max之间的关系,我们假设VEGF基因的变异与人成肌细胞,血浆VEGF中的VEGF基因表达有关。有氧运动训练前后的水平和Vo2max。本报告显示,VEGF启动子区单倍型在体外影响人成肌细胞中的VEGF基因表达。还发现在运动训练前后,老年男性和女性中VEGF启动子区域单倍型与Vo2max相关,其方式与VEGF基因表达实验的结果一致。此外,我们发现血浆VEGF水平与VEGF启动子区域单倍型无关,在有氧运动训练中血浆VEGF水平也不与基线Vo2max或DeltaVo2max相关。迄今为止,我们是第一个报道VEGF启动子区域单倍型影响人类成肌细胞中VEGF基因表达并与Vo2max相关的报道。这些结果对有氧运动训练有潜在的影响,也可能有助于了解不同细胞类型中VEGF启动子区域的功能。此外,这些结果可能在可能受血管生成影响的病理状况的研究中被证明是相关的,即肥胖,癌症,冠状动脉疾病和外周动脉疾病。

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