Key Laboratory of Laboratory Medicine, Ministry of Education, Zhejiang Provincial Key Laboratory of Medical Genetics, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, China.
Department of Clinical Laboratory, Wenzhou People's Hospital, Wenzhou, China.
J Clin Lab Anal. 2020 Jun;34(6):e23238. doi: 10.1002/jcla.23238. Epub 2020 Feb 13.
Most studies on cell-free DNA (cfDNA) were only for single body fluids; however, the differences in cfDNA distribution between two body fluids are rarely reported. Hence, in this work, we compared the differences in cfDNA distribution between cerebrospinal fluid (CSF) and serum of patients with brain-related diseases.
The fragment length of cfDNA was determined by using Agilent 2100 Bioanalyzer. The copy numbers of cell-free mitochondrial DNA (cf-mtDNA) and cell-free nuclear DNA (cf-nDNA) were determined by using real-time quantitative PCR (qPCR) and droplet digital PCR (ddPCR) with three pairs of mitochondrial ND1 and nuclear GAPDH primers, respectively.
There were short (60 bp), medium (167 bp), and long (>250 bp) cfDNA fragment length distributions totally obtained from CSF and serum using Agilent 2100 Bioanalyzer. The results of both qPCR and ddPCR confirmed the existence of these three cfDNA fragment ranges in CSF and serum. According to qPCR, the copy numbers of long cf-mtDNA, medium, and long cf-nDNA in CSF were significantly higher than in paired serum. In CSF, only long cf-mtDNA's copy numbers were higher than long cf-nDNA. But in serum, the copy numbers of medium and long cf-mtDNA were higher than the corresponding cf-nDNA.
The cf-nDNA and cf-mtDNA with different fragment lengths differentially distributed in the CSF and serum of patients with brain disorders, which might serve as a biomarker of human brain diseases.
大多数关于游离细胞 DNA(cfDNA)的研究仅针对单一体液;然而,两种体液之间 cfDNA 分布的差异很少有报道。因此,在这项工作中,我们比较了脑相关疾病患者脑脊液(CSF)和血清中 cfDNA 分布的差异。
使用 Agilent 2100 Bioanalyzer 测定 cfDNA 的片段长度。使用实时定量 PCR(qPCR)和液滴数字 PCR(ddPCR),分别使用三对线粒体 ND1 和核 GAPDH 引物,测定细胞游离线粒体 DNA(cf-mtDNA)和细胞游离核 DNA(cf-nDNA)的拷贝数。
使用 Agilent 2100 Bioanalyzer 从 CSF 和血清中总共获得了三种 cfDNA 片段长度分布:短(60 bp)、中(167 bp)和长(>250 bp)。qPCR 和 ddPCR 的结果均证实了 CSF 和血清中存在这三种 cfDNA 片段范围。根据 qPCR,CSF 中长 cf-mtDNA、中、长 cf-nDNA 的拷贝数明显高于配对血清。在 CSF 中,只有长 cf-mtDNA 的拷贝数高于长 cf-nDNA。但在血清中,中、长 cf-mtDNA 的拷贝数高于相应的 cf-nDNA。
不同片段长度的 cf-nDNA 和 cf-mtDNA 在脑疾病患者的 CSF 和血清中分布不同,可作为人类脑部疾病的生物标志物。