作者
David Andrijevic,Zvonimir Vrselja,Taras Lysyy,Shupei Zhang,Mario Skarica,Ana-Marija Spajic,David Dellal,Stephanie Thorn,Robert B. Duckrow,Shaojie Ma,Phan Q. Duy,Atagun U. Isiktas,Dan Liang,Mingfeng Li,Suel Kee Kim,Stefano G. Daniele,Khadija Banu,Sudhir Perincheri,Madhav C. Menon,Anita Huttner,Kevin N. Sheth,Kevin T Gobeske,Gregory T. Tietjen,Hitten P. Zaveri,Stephen R. Latham,Albert J. Sinusas,Nenad Sestan
摘要
After cessation of blood flow or similar ischaemic exposures, deleterious molecular cascades commence in mammalian cells, eventually leading to their death1,2. Yet with targeted interventions, these processes can be mitigated or reversed, even minutes or hours post mortem, as also reported in the isolated porcine brain using BrainEx technology3. To date, translating single-organ interventions to intact, whole-body applications remains hampered by circulatory and multisystem physiological challenges. Here we describe OrganEx, an adaptation of the BrainEx extracorporeal pulsatile-perfusion system and cytoprotective perfusate for porcine whole-body settings. After 1 h of warm ischaemia, OrganEx application preserved tissue integrity, decreased cell death and restored selected molecular and cellular processes across multiple vital organs. Commensurately, single-nucleus transcriptomic analysis revealed organ- and cell-type-specific gene expression patterns that are reflective of specific molecular and cellular repair processes. Our analysis comprises a comprehensive resource of cell-type-specific changes during defined ischaemic intervals and perfusion interventions spanning multiple organs, and it reveals an underappreciated potential for cellular recovery after prolonged whole-body warm ischaemia in a large mammal.