Reperfusion Activates AP-1 and Heat Shock Response in Donor Kidney Parenchyma after Warm Ischemia
Autor: | Alexandr Reznik, O. N. Reznik, Andrey Skvortsov, Ancha Baranova, Olga Plotnikova, Mikhail Skoblov |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Resuscitation Article Subject lcsh:Medicine 030230 surgery Kidney General Biochemistry Genetics and Molecular Biology Andrology 03 medical and health sciences 0302 clinical medicine Heat shock protein medicine Humans Warm Ischemia Heat shock Endoplasmic Reticulum Chaperone BiP General Immunology and Microbiology Warm Ischemia Time business.industry Gene Expression Profiling lcsh:R General Medicine medicine.disease Kidney Transplantation Perfusion Transcription Factor AP-1 030104 developmental biology medicine.anatomical_structure Reperfusion Injury business Reperfusion injury Heat-Shock Response Ex vivo Research Article |
Zdroj: | BioMed Research International, Vol 2018 (2018) BioMed Research International |
ISSN: | 2314-6141 2314-6133 |
DOI: | 10.1155/2018/5717913 |
Popis: | Utilization of kidneys from extended criteria donors leads to an increase in average warm ischemia time (WIT), which is associated with larger degrees of ischemia-reperfusion injury (IRI). Kidney resuscitation by extracorporeal perfusion in situ allows up to 60 minutes of asystole after the circulatory death. Molecular studies of kidney grafts from human donors with critically expanded WIT are warranted. Transcriptomes of two human kidneys from two different donors were profiled after 35-45 minutes of WIT and after 120 minutes of normothermic perfusion and compared. Baseline gene expression patterns in ischemic grafts display substantial intrinsic differences. IRI does not lead to substantial change in overall transcription landscape but activates a highly connected protein network with hubs centered on Jun/Fos/ATF transcription factors and HSP1A/HSPA5 heat shock proteins. This response is regulated by positive feedback. IRI networks are enriched in soluble proteins and biofluids assayable substances, thus, indicating feasibility of the longitudinal, minimally invasive assessment in vivo. Mapping of IRI related molecules in ischemic and reperfused kidneys provides a rationale for possible organ conditioning during machine assisted ex vivo normothermic perfusion. A study of natural diversity of the transcriptional landscapes in presumably normal, transplantation-suitable human organs is warranted. |
Databáze: | OpenAIRE |
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