Molecular Pathways Underlying Adaptive Repair of the Injured Kidney: Novel Donation After Cardiac Death and Acute Kidney Injury Platforms. Issue 2 (February 2020)

• Record Type: Journal Article
• Authors: Orlando, Giuseppe; Danger, Richard; Okut, Hayrettin; Edgar, Lauren; Bussolati, Benedetta; Gall, Emily; Bergman, Christopher R.; Tamburrini, Riccardo; Gazia, Carlo; Farney, Alan C.; Freedman, Barry I.; McPherson, Gwen; Rogers, Jeffrey; Stratta, Robert J.; Brouard, Sophie; Walker, Stephen J.
• Is Part Of: Annals of surgery. Volume 271:Issue 2(2020)
• Publication Date: 2020-02
• Subjects: adaptive repair -- AKI kidneys -- DCD kidneys -- gene expression -- kidney regeneration -- kidney repair -- kidney transplantation -- regenerative medicine; Surgery -- Periodicals; 617.005
• DOI: 10.1097/SLA.0000000000002946
• Languages: English
• ISSNs: 0003-4932

Abstract

Abstract : Objective: To test the hypothesis that gene expression profiling in peripheral blood from patients who have undergone kidney transplantation (KT) will provide mechanistic insights regarding graft repair and regeneration. Background: Renal grafts obtained from living donors (LD) typically function immediately, whereas organs from donation after cardiac death (DCD) or acute kidney injury (AKI) donors may experience delayed function with eventual recovery. Thus, recipients of LD, DCD, and AKI kidneys were studied to provide a more complete understanding of the molecular basis for renal recovery. Methods: Peripheral blood was collected from LD and DCD/AKI recipients before transplant and throughout the first 30 days thereafter. Total RNA was isolated and assayed on whole genome microarrays. Results: Comparison of longitudinal gene expression between LD and AKI/DCD revealed 2 clusters, representing 141 differentially expressed transcripts. A subset of 11 transcripts was found to be differentially expressed in AKI/DCD versus LD. In all recipients, the most robust gene expression changes were observed in the first day after transplantation. After day 1, gene expression profiles differed depending upon the source of the graft. In patients receiving LD grafts, the expression of most genes did not remain markedly elevated beyond the first day post-KT. In the AKI/DCD groups, elevations in gene expression were maintained for at least 5 days post-KT. In all recipients, the pattern of coordinate gene overexpression subsided by 28 to 30 days. Conclusions: Gene expression in peripheral blood of AKI/DCD recipients offers a novel platform to understand the potential mechanisms and timing of kidney repair and regeneration after transplantation.