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Zamorano, M.

Publications and source records attributed to Zamorano, M..

2 recordsLinked to original sources

Transcriptional and DNA Methylation Changes in the Hippocampus and Prefrontal Cortex after Fractionated Cranial Radiation in Mice

Fractionated whole-brain irradiation is essential for treating brain tumors, but many long-term survivors develop cognitive decline whose molecular basis is poorly understood. We asked which cell types and gene programs change late after irradiation, how the hippocampus and prefrontal cortex compare, and whether DNA methylation changes affect the same genes or programs. Male and female mice received whole-brain irradiation (5 x 4 Gy) or anesthesia alone. Irradiated mice showed persistent deficits in executive function and spatial memory. Eleven weeks after irradiation, single-nucleus RNA sequencing and whole-genome bisulfite sequencing of pooled hippocampal (CA1-3) and prefrontal tissue showed cell-type-specific transcriptional changes in neurons of both regions. Both regions showed reduced ribosomal-protein gene expression and changes in adhesion genes, with reduced respiratory-chain genes in prefrontal neurons and bidirectional synaptic gene changes in hippocampus. Differentially methylated regions were enriched at promoters, with hypermethylation predominating in three of the four sex-by-region contrasts. Methylation and gene expression changes pointed to overlapping synaptic and signaling programs, largely through different genes.

neuroscience↗

Developmental Stage-Dependent Transcriptomic Responses to Neonatal Intraventricular Hemorrhage

Neonatal intraventricular hemorrhage (IVH) is a major complication of preterm birth, yet how developmental stage influences the brains response to injury remains unclear. We performed single-nucleus RNA sequencing on rat brains 24 hours after IVH at postnatal day 2 (PND2) or day 5 (PND5) to define transcriptional responses across cell types. We identified 42 distinct cell populations and found that PND5 brains exhibited a markedly stronger immune and inflammatory response to IVH, with a threefold increase in differentially expressed genes compared to PND2. Microglia were the most perturbed cell type at both stages, showing increased oxidative stress and polarization toward both pro- and anti-inflammatory phenotypes at PND5. Ligand-receptor and regulon analysis revealed a shift from reparative IGF2 and TGF-{beta} signaling at PND2 to proinflammatory Wnt signaling and activation of Runx1 and Stat5 at PND5. These findings highlight the importance of developmental timing in shaping the neuroimmune response to IVH and identify potential stage-specific therapeutic targets.

neuroscience↗