Department of Sports Medicine, Disease Prevention and Rehabilitation, Johannes Gutenberg-University Mainz, Mainz, Germany.
Department of Internal Medicine III, Hematology, Oncology and Pneumology, University Medical Center, Johannes Gutenberg-University, Mainz, Germany.
Exerc Immunol Rev. 2015;21:164-73.
The role of cell free DNA (cfDNA) has been intensively discussed under various pathological conditions and after acute bouts of exercise. To date, there is still no conclusive evidence concerning the cellular origin of cfDNA and the entire mechanism leading to elevated cfDNA concentrations in human plasma and serum. Here, we investigated the cellular origin of cfDNA in sex-mismatched haematopoietic stem cell transplantation (HSCT) and liver transplantation (LT) patients by determining the relative proportion of Y-chromosomal to total nuclear cfDNA. Total nuclear cfDNA and Y-chromosomal cfDNA concentrations were determined in blood plasma before and after an incremental exercise test via quantitative real-time PCR (qPCR). Female HSCT patients showed high proportions of Y-chromosomal cfDNA. Both total nuclear and Y-chromosomal cfDNA increased significantly and in a highly correlated fashion due to exercise. In male HSCT patients with female donors less than 10% of the cfDNA was of Y-chromosomal origin at any point in time and even though the total amount of cfDNA increased during exercise, no increases in Y-chromosomal DNA could be detected. The percentage of Y-chromosomal cfDNA in female LT patients with male donors was very low and levels remained unchanged during exercise. This indicates that cells not derived from the bone marrow, in this case transplanted liver cells, represented only a minor fraction of cfDNA in blood plasma and were not released during acute physical exercise. Even though many physiological conditions may be altered in transplant patients versus healthy people, our results strongly suggest that cells from the haematopoietic lineage are the main source of cfDNA released during acute bouts of exercise.
无细胞游离 DNA(cfDNA)在各种病理条件下以及急性运动后都被广泛研究。迄今为止,关于 cfDNA 的细胞来源以及导致人血浆和血清中 cfDNA 浓度升高的整个机制仍没有确凿的证据。在这里,我们通过确定 Y 染色体与总核 cfDNA 的相对比例,研究了性不匹配造血干细胞移植(HSCT)和肝移植(LT)患者 cfDNA 的细胞来源。通过定量实时 PCR(qPCR),在递增运动试验前后,我们测定了血浆中总核 cfDNA 和 Y 染色体 cfDNA 的浓度。女性 HSCT 患者表现出高比例的 Y 染色体 cfDNA。由于运动,总核和 Y 染色体 cfDNA 均显著增加,且呈高度相关的方式增加。在女性供体的男性 HSCT 患者中,在任何时间点,cfDNA 的 Y 染色体来源都不到 10%,尽管运动期间 cfDNA 的总量增加,但无法检测到 Y 染色体 DNA 的增加。男性供体的女性 LT 患者的 Y 染色体 cfDNA 百分比非常低,且在运动期间保持不变。这表明,在这种情况下,源自移植肝脏细胞的非骨髓细胞仅代表血浆中 cfDNA 的一小部分,并且不会在急性体力活动中释放。尽管移植患者与健康人相比,许多生理条件可能会发生改变,但我们的结果强烈表明,造血谱系的细胞是急性运动期间释放的 cfDNA 的主要来源。