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Cellular recovery after prolonged warm ischaemia of the whole body.
Andrijevic, David; Vrselja, Zvonimir; Lysyy, Taras; Zhang, Shupei; Skarica, Mario; Spajic, Ana; Dellal, David; Thorn, Stephanie L; Duckrow, Robert B; Ma, Shaojie; Duy, Phan Q; Isiktas, Atagun U; Liang, Dan; Li, Mingfeng; Kim, Suel-Kee; Daniele, Stefano G; Banu, Khadija; Perincheri, Sudhir; Menon, Madhav C; Huttner, Anita; Sheth, Kevin N; Gobeske, Kevin T; Tietjen, Gregory T; Zaveri, Hitten P; Latham, Stephen R; Sinusas, Albert J; Sestan, Nenad.
Affiliation
  • Andrijevic D; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Vrselja Z; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Lysyy T; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Zhang S; Department of Surgery, Yale School of Medicine New Haven, New Haven, CT, USA.
  • Skarica M; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Spajic A; Department of Genetics, Yale School of Medicine, New Haven, CT, USA.
  • Dellal D; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Thorn SL; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Duckrow RB; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Ma S; Department of Biomedical Engineering, Yale University, New Haven, CT, USA.
  • Duy PQ; Yale Translational Research Imaging Center, Department of Medicine, Yale School of Medicine, New Haven, CT, USA.
  • Isiktas AU; Department of Neurology, Yale University School of Medicine, New Haven, CT, USA.
  • Liang D; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Li M; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Kim SK; Department of Neurosurgery, Yale School of Medicine, New Haven, CT, USA.
  • Daniele SG; Medical Scientist Training Program (MD-PhD), Yale School of Medicine, New Haven, CT, USA.
  • Banu K; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Perincheri S; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Menon MC; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Huttner A; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Sheth KN; Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
  • Gobeske KT; Medical Scientist Training Program (MD-PhD), Yale School of Medicine, New Haven, CT, USA.
  • Tietjen GT; Department of Nephrology, Yale School of Medicine, New Haven, CT, USA.
  • Zaveri HP; Department of Pathology, Yale School of Medicine, New Haven, CT, USA.
  • Latham SR; Department of Nephrology, Yale School of Medicine, New Haven, CT, USA.
  • Sinusas AJ; Department of Pathology, Yale School of Medicine, New Haven, CT, USA.
  • Sestan N; Department of Neurology, Yale University School of Medicine, New Haven, CT, USA.
Nature ; 608(7922): 405-412, 2022 08.
Article in En | MEDLINE | ID: mdl-35922506
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Perfusion / Swine / Cell Survival / Cytoprotection / Warm Ischemia Limits: Animals Language: En Journal: Nature Year: 2022 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Perfusion / Swine / Cell Survival / Cytoprotection / Warm Ischemia Limits: Animals Language: En Journal: Nature Year: 2022 Document type: Article Affiliation country: Estados Unidos
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