| Literature DB >> 32627324 |
Jenna R DiRito1,2, Sarah A Hosgood1, Melanie Reschke3, Claire Albert4, Laura G Bracaglia4, John R Ferdinand5, Benjamin J Stewart5, Christopher M Edwards2, Anand G Vaish2, Sathia Thiru6, David C Mulligan2, Danielle J Haakinson2, Menna R Clatworthy5, W Mark Saltzman4, Jordan S Pober7, Michael L Nicholson1, Gregory T Tietjen2,4.
Abstract
Thousands of kidneys from higher-risk donors are discarded annually because of the increased likelihood of complications posttransplant. Given the severe organ shortage, there is a critical need to improve utilization of these organs. To this end, normothermic machine perfusion (NMP) has emerged as a platform for ex vivo assessment and potential repair of marginal organs. In a recent study of 8 transplant-declined human kidneys on NMP, we discovered microvascular obstructions that impaired microvascular blood flow. However, the nature and physiologic impact of these lesions were unknown. Here, in a study of 39 human kidneys, we have identified that prolonged cold storage of human kidneys induces accumulation of fibrinogen within tubular epithelium. Restoration of normoxic conditions-either ex vivo during NMP or in vivo following transplant-triggered intravascular release of fibrinogen correlating with red blood cell aggregation and microvascular plugging. Combined delivery of plasminogen and tissue plasminogen activator during NMP lysed the plugs leading to a significant reduction in markers of renal injury, improvement in indicators of renal function, and improved delivery of vascular-targeted nanoparticles. Our study suggests a new mechanism of cold storage injury in marginal organs and provides a simple treatment with immediate translational potential.Entities:
Keywords: basic (laboratory) research/science; coagulation and hemostasis; disease pathogenesis; kidney biology; kidney transplantation/nephrology; thrombolytic therapy/thrombolysis; translational research/science; vascular biology
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Year: 2020 PMID: 32627324 PMCID: PMC7775334 DOI: 10.1111/ajt.16148
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086