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Genome-wide DNA methylation and transcriptomic analysis of liver tissues subjected to early ischemia/reperfusion injury upon human liver transplantation.
Giraudi, Pablo J; Laraño, Allen A; Monego, Simeone Dal; Pravisani, Riccardo; Bonazza, Deborah; Gondolesi, Gabriel; Tiribelli, Claudio; Baralle, Francisco; Baccarani, Umberto; Licastro, Danilo.
Afiliação
  • Giraudi PJ; Metabolic Liver Disease Unit, Fondazione Italiana Fegato, Trieste, Italy. Electronic address: pablo.giraudi@fegato.it.
  • Laraño AA; Metabolic Liver Disease Unit, Fondazione Italiana Fegato, Trieste, Italy; Research Institute for Tropical Medicine, Department of Health, Muntinlupa City, Philippines.
  • Monego SD; Area Science Park, Trieste, Italy.
  • Pravisani R; Liver-Kidney Transplant Unit, Department of Medicine, University of Udine, Italy.
  • Bonazza D; Anatomia ed Istologia Patologica, Cattinara Hospital, ASUGI, Trieste, Italy.
  • Gondolesi G; Instituto de Medicina Traslacional, Trasplante y Bioingeniería, Universidad Favaloro, Buenos Aires, Argentina.
  • Tiribelli C; Metabolic Liver Disease Unit, Fondazione Italiana Fegato, Trieste, Italy.
  • Baralle F; Metabolic Liver Disease Unit, Fondazione Italiana Fegato, Trieste, Italy.
  • Baccarani U; Liver-Kidney Transplant Unit, Department of Medicine, University of Udine, Italy.
  • Licastro D; Area Science Park, Trieste, Italy.
Ann Hepatol ; 29(4): 101506, 2024.
Article em En | MEDLINE | ID: mdl-38710471
ABSTRACT
INTRODUCTION AND

OBJECTIVES:

Epigenetic changes represent a mechanism connecting external stresses with long-term modifications of gene expression programs. In solid organ transplantation, ischemia-reperfusion injury (IRI) appears to induce epigenomic changes in the graft, although the currently available data are extremely limited. The present study aimed to characterize variations in DNA methylation and their effects on the transcriptome in liver transplantation from brain-dead donors. PATIENTS AND

METHODS:

12 liver grafts were evaluated through serial biopsies at different timings in the procurement-transplantation process T0 (warm procurement, in donor), T1 (bench surgery), and T2 (after reperfusion, in recipient). DNA methylation (DNAm) and transcriptome profiles of biopsies were analyzed using microarrays and RNAseq.

RESULTS:

Significant variations in DNAm were identified, particularly between T2 and T0. Functional enrichment of the best 1000 ranked differentially methylated promoters demonstrated that 387 hypermethylated and 613 hypomethylated promoters were involved in spliceosomal assembly and response to biotic stimuli, and inflammatory immune responses, respectively. At the transcriptome level, T2 vs. T0 showed an upregulation of 337 and downregulation of 61 genes, collectively involved in TNF-α, NFKB, and interleukin signaling. Cell enrichment analysis individuates macrophages, monocytes, and neutrophils as the most significant tissue-cell type in the response.

CONCLUSIONS:

In the process of liver graft procurement-transplantation, IRI induces significant epigenetic changes that primarily act on the signaling pathways of inflammatory responses dependent on TNF-α, NFKB, and interleukins. Our DNAm datasets are the early IRI methylome literature and will serve as a launch point for studying the impact of epigenetic modification in IRI.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Traumatismo por Reperfusão / Transplante de Fígado / Metilação de DNA / Perfilação da Expressão Gênica / Epigênese Genética / Fígado Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de publicação: México

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Traumatismo por Reperfusão / Transplante de Fígado / Metilação de DNA / Perfilação da Expressão Gênica / Epigênese Genética / Fígado Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Hepatol Assunto da revista: GASTROENTEROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de publicação: México