| Literature DB >> 35922506 |
David Andrijevic1, Zvonimir Vrselja1, Taras Lysyy1,2, Shupei Zhang1,3, Mario Skarica1, Ana Spajic1, David Dellal1,4, Stephanie L Thorn5, Robert B Duckrow6, Shaojie Ma1, Phan Q Duy1,7,8, Atagun U Isiktas1, Dan Liang1, Mingfeng Li1, Suel-Kee Kim1, Stefano G Daniele1,8, Khadija Banu9, Sudhir Perincheri10, Madhav C Menon9, Anita Huttner10, Kevin N Sheth6,7, Kevin T Gobeske6, Gregory T Tietjen2,4, Hitten P Zaveri6, Stephen R Latham11, Albert J Sinusas3,4,12,13, Nenad Sestan14,15,16,17,18,19.
Abstract
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.Entities:
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Year: 2022 PMID: 35922506 PMCID: PMC9518831 DOI: 10.1038/s41586-022-05016-1
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 69.504