TY - JOUR
T1 - The Spatially Resolved Kidney Transcriptome Signatures in Rat Models of Trauma-Induced Acute Kidney Injury
AU - Isnard, Pierre
AU - Laemmel, Elisabeth
AU - Martinez, Thibault
AU - Bergis, Benjamin
AU - Harrois, Anatole
AU - Huertas, Alice
AU - Li, Dian
AU - Humphreys, Benjamin D.
AU - Libert, Nicolas
N1 - Publisher Copyright:
© 2025
PY - 2025
Y1 - 2025
N2 - Background: – Trauma is a leading global cause of death, and acute kidney injury (AKI) significantly worsens outcomes. Hemorrhagic shock (HS) and rhabdomyolysis (RM) are major contributors, yet their individual and combined effects on the kidney remain poorly defined.Methods: – Using a clinically relevant rat model that closely mimics human trauma, we performed bulk and spatial transcriptomics to characterize early renal responses to HS, RM, and their combination (RM-HS). Commercial mouse spatial transcriptomics probes were successfully applied to rat kidney tissue, enabling cost-effective and region-specific gene expression profiling.Results: – RM emerged as the dominant driver of transcriptional changes, while RM-HS triggered a synergistic, mortality-associated response. Comparative analyses revealed distinct regional and molecular signatures: HS suppressed metabolic activity, whereas RM induced widespread upregulation of inflammatory and stress-response pathways.Conclusions: – We propose a mechanistic framework linking these traumatic insults to tubular cell injury and death, with mitochondrial dysfunction, dysregulated lipid metabolism, PLIN2 expression, and ferroptosis as central components. This integrative model advances our understanding of trauma-induced renal injury and may enable the identification of novel biomarkers and therapeutic strategies to mitigate AKI severity in trauma patients.
AB - Background: – Trauma is a leading global cause of death, and acute kidney injury (AKI) significantly worsens outcomes. Hemorrhagic shock (HS) and rhabdomyolysis (RM) are major contributors, yet their individual and combined effects on the kidney remain poorly defined.Methods: – Using a clinically relevant rat model that closely mimics human trauma, we performed bulk and spatial transcriptomics to characterize early renal responses to HS, RM, and their combination (RM-HS). Commercial mouse spatial transcriptomics probes were successfully applied to rat kidney tissue, enabling cost-effective and region-specific gene expression profiling.Results: – RM emerged as the dominant driver of transcriptional changes, while RM-HS triggered a synergistic, mortality-associated response. Comparative analyses revealed distinct regional and molecular signatures: HS suppressed metabolic activity, whereas RM induced widespread upregulation of inflammatory and stress-response pathways.Conclusions: – We propose a mechanistic framework linking these traumatic insults to tubular cell injury and death, with mitochondrial dysfunction, dysregulated lipid metabolism, PLIN2 expression, and ferroptosis as central components. This integrative model advances our understanding of trauma-induced renal injury and may enable the identification of novel biomarkers and therapeutic strategies to mitigate AKI severity in trauma patients.
UR - https://www.scopus.com/pages/publications/105027780458
U2 - 10.34067/KID.0000001045
DO - 10.34067/KID.0000001045
M3 - Article
C2 - 41396698
AN - SCOPUS:105027780458
SN - 2641-7650
VL - Publish Ahead of Print
JO - Kidney360
JF - Kidney360
ER -