Center for Engineering in Medicine, Harvard Medical School and Massachusetts General Hospital, Boston, MA, USA.
Shriners Hospitals for Children - Boston, Boston, MA, USA.
Sci Rep. 2020 Jan 24;10(1):1102. doi: 10.1038/s41598-020-57589-4.
The global shortage of donor organs has made it crucial to deeply understand and better predict donor liver viability. However, biomarkers that effectively assess viability of marginal grafts for organ transplantation are currently lacking. Here, we showed that hepatocytes, sinusoidal endothelial, stellate, and liver-specific immune cells were released into perfusates from Lewis rat livers as a result of cold ischemia and machine perfusion. Perfusate comparison analysis of fresh livers and cold ischemic livers showed that the released cell profiles were significantly altered by the duration of cold ischemia. Our findings show for the first time that parenchymal cells are released from organs under non-proliferative pathological conditions, correlating with the degree of ischemic injury. Thus, perfusate cell profiles could serve as potential biomarkers of graft viability and indicators of specific injury mechanisms during organ handling and transplantation. Further, parenchymal cell release may have applications in other pathological conditions beyond organ transplantation.
全球捐献器官短缺,因此深入了解和更好地预测供肝活力至关重要。然而,目前缺乏有效评估边缘供体器官移植活力的生物标志物。在这里,我们发现冷缺血和机器灌注会导致Lewis 大鼠肝脏中的肝细胞、窦内皮细胞、星状细胞和肝脏特异性免疫细胞释放到灌流液中。新鲜肝脏和冷缺血肝脏的灌流液比较分析表明,冷缺血时间会显著改变释放细胞的特征。我们的研究结果首次表明,实质细胞在非增殖性病理条件下从器官中释放出来,与缺血损伤程度相关。因此,灌流液细胞特征可以作为移植物活力的潜在生物标志物,以及器官处理和移植过程中特定损伤机制的指标。此外,实质细胞的释放可能在器官移植以外的其他病理情况下具有应用价值。