Cillo Umberto, Lonati Caterina, Bertacco Alessandra, Magnini Lucrezia, Battistin Michele, Borsetto Lara, Dazzi Francesco, Al-Adra David, Gringeri Enrico, Bacci Maria Laura, Schlegel Andrea, Dondossola Daniele
Hepato-Biliary-Pancreatic Surgery and Liver Transplant Unit, General Surgery 2, Department of Surgical, Oncological and Gastroenterological Sciences, University of Padua, Padua, Italy.
Center for Preclinical Research, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Via Pace 9, 20100, Milan, Italy.
Nat Commun. 2025 Jan 2;16(1):283. doi: 10.1038/s41467-024-55217-7.
To fully harness mesenchymal-stromal-cells (MSCs)' benefits during Normothermic Machine Perfusion (NMP), we developed an advanced NMP platform coupled with a MSC-bioreactor and investigated its bio-molecular effects and clinical feasibility using rat and porcine models. The study involved three work packages: 1) Development (n = 5): MSC-bioreactors were subjected to 4 h-liverless perfusion; 2) Rat model (n = 10): livers were perfused for 4 h on the MSC-bioreactor-circuit or with the standard platform; 3) Porcine model (n = 6): livers were perfused using a clinical device integrated with a MSC-bioreactor or in its standard setup. MSCs showed intact stem-core properties after liverless-NMP. Liver NMP induced specific, liver-tailored, changes in MSCs' secretome. Rat livers exposed to bioreactor-based perfusion produced more bile, released less damage and pro-inflammatory biomarkers, and showed improved mithocondrial function than those subjected to standard NMP. MSC-bioreactor integration into a clinical device resulted in no machine failure and perfusion-related injury. This proof-of-concept study presents a novel MSC-based liver NMP platform that could reduce the deleterious effects of ischemia/reperfusion before transplantation.
为了在常温机器灌注(NMP)过程中充分利用间充质基质细胞(MSC)的益处,我们开发了一个与MSC生物反应器相结合的先进NMP平台,并使用大鼠和猪模型研究了其生物分子效应和临床可行性。该研究包括三个工作包:1)开发(n = 5):对MSC生物反应器进行4小时无肝灌注;2)大鼠模型(n = 10):在MSC生物反应器回路或标准平台上对肝脏进行4小时灌注;3)猪模型(n = 6):使用与MSC生物反应器集成的临床设备或其标准设置对肝脏进行灌注。在无肝NMP后,MSC显示出完整的干细胞核心特性。肝脏NMP诱导了MSC分泌组中特定的、针对肝脏的变化。与接受标准NMP的大鼠肝脏相比,接受基于生物反应器灌注的大鼠肝脏产生了更多胆汁,释放的损伤和促炎生物标志物更少,并且线粒体功能得到改善。将MSC生物反应器集成到临床设备中未导致机器故障和灌注相关损伤。这项概念验证研究提出了一种基于MSC的新型肝脏NMP平台,该平台可以减少移植前缺血/再灌注的有害影响。