• Jesse A Davidson, John Iguidbashian, Ludmila Khailova, Tanner Lehmann, Alejandro Suarez-Pierre, Lindsay M Thomson, Jack Zakrzewski, Eiman Ali, Schuyler Lee, Benjamin S Frank, Richard J Ing, Matthew L Stone, Suzanne Osorio Lujan, Sierra Niemiec, and Christopher A Mancuso.
• University of Colorado School of Medicine, Aurora, CO, Department of Pediatrics, USA. Electronic address: jesse.davidson@childrenscolorado.org.
• Transl Res. 2025 Mar 1; 277: 647464-74.

AbstractThe organ-level molecular response to cardiac surgery with cardiopulmonary bypass (CPB) remains inadequately understood and may be heterogeneous. Here, we measured organ-specific gene expression in a piglet model of CPB with deep hypothermic circulatory arrest (DHCA). Infant piglets underwent peripheral CPB with 75 min of DHCA and 6 h of critical care after separation from CPB. Mechanically ventilated animals served as controls. Tissue was obtained from the lung, kidney, liver, heart, and ileum. RNA sequencing was performed using NovaSeq 6000 and evaluated via differentially expressed gene (DEG) and pathway/network analyses. CPB/DHCA induced significant transcriptomic alterations, with greater changes seen in liver (2,166 DEGs), heart (775 DEGs), and kidney (1,759 DEGs) compared to lung (401 DEGs) and ileum (11 DEGs), and little overlap across organs (<20 % differentially expressed in >1 organ). Key upregulated systems included ribosomal proliferation and mitochondrial assembly in the liver, oxidative stress response and proximal tubular repair in the kidney, myofilament structural genes and pro-hypertrophy pathways in the heart, and solute channels and arginine metabolism in the lung. Downregulation of adaptive immunity genes occurred in multiple organs. Transcriptomics could inform the investigation of targeted therapies and adverse event screening after cardiac surgery.Copyright © 2025 Elsevier Inc. All rights reserved.

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