Literature DB >> 28388830

The release of microRNA-122 during liver preservation is associated with early allograft dysfunction and graft survival after transplantation.

Jasmijn W Selten1, Cornelia J Verhoeven1, Veerle Heedfeld2, Henk P Roest1, Jeroen de Jonge1, Jacques Pirenne2, Jos van Pelt3, Jan N M Ijzermans1, Diethard Monbaliu2, Luc J W van der Laan1.   

Abstract

Early allograft dysfunction (EAD) after liver transplantation (LT) is associated with inferior graft survival. EAD is more prevalent in grafts from donation after circulatory death (DCD). However, accurate prediction of liver function remains difficult because of the lack of specific biomarkers. Recent experimental and clinical studies highlight the potential of hepatocyte-derived microRNAs (miRNAs) as sensitive, stable, and specific biomarkers of liver injury. The aim of this study was to determine whether miRNAs in graft preservation fluid are predictive for EAD after clinical LT and in an experimental DCD model. Graft preservation solutions of 83 liver grafts at the end of cold ischemia were analyzed for miRNAs by reverse transcription polymerase chain reaction. Of these grafts, 42% developed EAD after transplantation. Results were verified in pig livers (n = 36) exposed to different lengths of warm ischemia time (WIT). The absolute miR-122 levels and miR-122/miR-222 ratios in preservation fluids were significantly higher in DCD grafts (P = 0.001) and grafts developing EAD (P = 0.004). In concordance, the miR-122/miR-222 ratios in perfusion fluid correlate with serum transaminase levels within the first 24 hours after transplantation. Longterm graft survival was significantly diminished in grafts with high miR-122/miR-222 ratios (P = 0.02). In the porcine DCD model, increased WIT lead to higher absolute miR-122 levels and relative miR-122/miR-222 ratios in graft perfusion fluid (P = 0.01 and P = 0.02, respectively). High miR-122/miR-222 ratios in pig livers were also associated with high aspartate aminotransferase levels after warm oxygenated reperfusion. In conclusion, both absolute and relative miR-122 levels in graft preservation solution are associated with DCD, EAD, and early graft loss after LT. As shown in a porcine DCD model, miRNA release correlated with the length of WITs. Liver Transplantation 23 946-956 2017 AASLD.
© 2017 by the American Association for the Study of Liver Diseases.

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Year:  2017        PMID: 28388830     DOI: 10.1002/lt.24766

Source DB:  PubMed          Journal:  Liver Transpl        ISSN: 1527-6465            Impact factor:   5.799


  13 in total

1.  Hypoxia-inducible factor-1α-dependent induction of miR122 enhances hepatic ischemia tolerance.

Authors:  Cynthia Ju; Meng Wang; Eunyoung Tak; Boyun Kim; Christoph Emontzpohl; Yang Yang; Xiaoyi Yuan; Huban Kutay; Yafen Liang; David R Hall; Wasim A Dar; J Steve Bynon; Peter Carmeliet; Kalpana Ghoshal; Holger K Eltzschig
Journal:  J Clin Invest       Date:  2021-04-01       Impact factor: 14.808

2.  Liver Ischemia and Reperfusion Induce Periportal Expression of Necroptosis Executor pMLKL Which Is Associated With Early Allograft Dysfunction After Transplantation.

Authors:  Shaojun Shi; Eliano Bonaccorsi-Riani; Ivo Schurink; Thierry van den Bosch; Michael Doukas; Karishma A Lila; Henk P Roest; Daela Xhema; Pierre Gianello; Jeroen de Jonge; Monique M A Verstegen; Luc J W van der Laan
Journal:  Front Immunol       Date:  2022-05-17       Impact factor: 8.786

3.  Peritransplant kinetics of Mac-2-binding protein glycosylation isomer levels in living donor liver transplantation: its implication of posttransplant small-for-size syndrome.

Authors:  Hideaki Uchiyama; Ken Shirabe; Yuki Bekki; Takeo Toshima; Norifumi Harimoto; Toru Ikegami; Tomoharu Yoshizumi
Journal:  Transl Gastroenterol Hepatol       Date:  2019-05-25

4.  The Macrophage Activation Marker Soluble CD163 is Associated With Early Allograft Dysfunction After Liver Transplantation.

Authors:  Karen L Thomsen; Francis P Robertson; Peter Holland-Fischer; Brian R Davidson; Rajeshwar P Mookerjee; Holger J Møller; Rajiv Jalan; Henning Grønbæk
Journal:  J Clin Exp Hepatol       Date:  2018-10-05

Review 5.  Current review of machine perfusion in liver transplantation from the Japanese perspective.

Authors:  Noboru Harada; Tomoharu Yoshizumi; Masaki Mori
Journal:  Surg Today       Date:  2021-03-22       Impact factor: 2.549

Review 6.  Novel Targets for Treating Ischemia-Reperfusion Injury in the Liver.

Authors:  Weili Yang; Ji Chen; Yuhong Meng; Zhenzhen Chen; Jichun Yang
Journal:  Int J Mol Sci       Date:  2018-04-26       Impact factor: 5.923

7.  Cell-free microRNAs as early predictors of graft viability during ex vivo normothermic machine perfusion of human donor livers.

Authors:  Alix P M Matton; Jasmijn W Selten; Henk P Roest; Jeroen de Jonge; Jan N M IJzermans; Vincent E de Meijer; Robert J Porte; Luc J W van der Laan
Journal:  Clin Transplant       Date:  2020-02-20       Impact factor: 2.863

Review 8.  Assessment of Organ Quality in Kidney Transplantation by Molecular Analysis and Why It May Not Have Been Achieved, Yet.

Authors:  Seraina von Moos; Enver Akalin; Valeria Mas; Thomas F Mueller
Journal:  Front Immunol       Date:  2020-05-12       Impact factor: 7.561

9.  Inhibition of miRNA-222-3p Relieves Staphylococcal Enterotoxin B-Induced Liver Inflammatory Injury by Upregulating Suppressors of Cytokine Signaling 1.

Authors:  Peng Zhang; Jingda Yu; Yifang Gui; Cui Sun; Weiping Han
Journal:  Yonsei Med J       Date:  2019-11       Impact factor: 2.759

10.  Comprehensive Evaluation of a Donated After Circulatory Death (DCD) Donor Liver Model in Minipigs.

Authors:  Guang Wang; Ying Cheng; Yongfeng Liu
Journal:  Ann Transplant       Date:  2018-10-30       Impact factor: 1.530

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