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The lipidomic architecture of the mouse brain
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The lipidomic architecture of the mouse brain

Luca Fusar Bassini, Halima Hannah Schede, Laura Capolupo +12 more
October 2025
 ·
bioRxiv
 ·
DOI 
10.1101/2025.10.13.682018
94
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Reproducible
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It ranks in the top 1% of preprints assessed in Systems Biology this quarter.
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Why this is interesting

This whole-brain lipid atlas at micrometric resolution overturns the view that transcriptomics captures brain biochemical organization, revealing that membrane lipids define an independent spatial architecture—one that adapts dynamically to physiological states like pregnancy.

QED claims analysis

Summary

High-resolution spatial lipidomics reveals that the mouse brain is organized into 539 spatially coherent lipid territories (lipizones) that align with functional anatomy, capture both cell bodies and their distal axon terminals to reveal connectivity patterns inaccessible to transcriptomics, and undergo coordinated large-scale reorganization during pregnancy, establishing membrane lipid composition as a dynamic architectural dimension of brain organization that is irreducible to gene expression.

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Main Claim 1 –

Lipizones Define Spatial Lipid Territories Aligned with Brain Anatomy

Supporting evidence

  • Gray-Matter Lipizones Follow an Interior–Exterior Anatomical Organization
  • Oligodendrocyte Lipids Drive Unexpected Regional White-Matter Diversity
  • Ventricular System Shows Lipid Zonation with Sphingomyelin Markers
Main Claim 2 –

Lipizones Link Somata and Distal Terminals to Reveal Connectivity

Supporting evidence

  • Brain Lipidome Is Poorly Predicted by Transcriptome or Enzymes
Main Claim 3 –

Pregnancy Drives Coordinated, Brain-Wide Lipidomic Reorganization

Supporting evidence

  • Pregnancy-Induced Lipidome Changes Exceed Baseline Sex Differences

Abstract

Lipids are fundamental components of the brain, crucial for synaptic transmission and signal propagation. Altered brain lipid composition is associated with common and rare neuropathologies, yet, the spatial organization of the mammalian brain lipidome remains insufficiently characterized compared to other modalities. Here, we mapped the membrane lipid architecture of the adult mouse brain at micrometric scale, across sexes, and during pregnancy. This Lipid Brain Atlas reveals that lipids define a fine-grained biochemical structure that aligns with functional anatomy. Membrane lipid spatial heterogeneity clusters into territories, which we termed lipizones. Lipizones partially mirror cell type territories, but also capture distal axon terminals. Through lipizones, (i) we reveal the organizing principles of the gray matter lipidome, related to connectivity and cytoarchitecture; (ii) we discover a new axis of oligodendrocyte heterogeneity in the white matter; (iii) and we find biochemical zonation in the choroid plexus and in the ventricular walls. We show that this lipidomic architecture can adapt to changing physiological needs. In the brain of pregnant females, the white matter is metabolically activated and the outer cortex is reorganized. These results are a foundational resource (https://lbae-v2.epfl.ch/), poised to reshape our understanding of lipids in brain development, physiology, and pathology.

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