Institute of Molecular Biomedicine, Faculty of Medicine, Comenius University, Sasinkova 4, 811 08 Bratislava, Slovakia.
Institute of Physiology, Faculty of Medicine, Comenius University, Sasinkova 2, 813 72 Bratislava, Slovakia.
Int J Mol Sci. 2019 Aug 26;20(17):4163. doi: 10.3390/ijms20174163.
Extracellular DNA (ecDNA) is studied as a possible biomarker, but also as a trigger of the immune responses important for the pathogenesis of several diseases. Extracellular deoxyribonuclease (DNase) activity cleaves ecDNA. The aim of our study was to describe the interindividual variability of ecDNA and DNase activity in the plasma of healthy mice, and to analyze the potential determinants of the variability, including sex, age, and bodyweight. In this experiment, 58 adult CD1 mice (41 females and 31 males) of a variable age (3 to 16 months old) and bodyweight (females 25.7 to 52.1 g, males 24.6 to 49.6 g) were used. The plasma ecDNA was measured using a fluorometric method. The nuclear ecDNA and mitochondrial ecDNA were quantified using real-time PCR. The deoxyribonuclease activity was assessed using the single radial enzyme diffusion method. The coefficient of variance for plasma ecDNA was 139%, and for DNase 48%. Sex differences were not found in the plasma ecDNA (52.7 ± 73.0 ηg/mL), but in the DNase activity (74.5 ± 33.5 K.u./mL for males, and 47.0 ± 15.4 K.u./mL for females). There were no associations between plasma ecDNA and bodyweight or the age of mice. Our study shows that the variability of plasma ecDNA and DNase in adult healthy mice is very high. Sex, age, and bodyweight seem not to be major determinants of ecDNA variability in healthy mice. As ecDNA gains importance in the research of several diseases, it is of importance to understand its production and cleavage. Further studies should, thus, test other potential determinants, taking into account cleavage mechanisms other than DNase.
细胞外 DNA(ecDNA)不仅被研究为一种可能的生物标志物,还被研究为触发几种疾病发病机制中免疫反应的因素。细胞外脱氧核糖核酸酶(DNase)活性可切割 ecDNA。本研究旨在描述健康小鼠血浆中 ecDNA 和 DNase 活性的个体间变异性,并分析包括性别、年龄和体重在内的潜在变异性决定因素。在该实验中,使用了年龄(3 至 16 个月)和体重(雌性 25.7 至 52.1g,雄性 24.6 至 49.6g)不同的 58 只成年 CD1 小鼠(41 只雌性和 31 只雄性)。使用荧光法测量血浆 ecDNA。使用实时 PCR 定量核 ecDNA 和线粒体 ecDNA。使用单径向酶扩散法评估脱氧核糖核酸酶活性。血浆 ecDNA 的变异系数为 139%,DNase 为 48%。在血浆 ecDNA(52.7 ± 73.0 ηg/mL)中未发现性别差异,但在 DNase 活性(雄性 74.5 ± 33.5 K.u./mL,雌性 47.0 ± 15.4 K.u./mL)中存在差异。血浆 ecDNA 与体重或小鼠年龄之间无相关性。本研究表明,成年健康小鼠血浆 ecDNA 和 DNase 的变异性非常高。性别、年龄和体重似乎不是健康小鼠 ecDNA 变异性的主要决定因素。由于 ecDNA 在几种疾病的研究中变得越来越重要,因此了解其产生和切割至关重要。因此,进一步的研究应该考虑其他潜在的决定因素,包括除 DNase 以外的其他切割机制。