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Table 2 Cell type-specific sex-dependent gene expression changes across major brain cell types in THY-Tau22 mice at 17 months of age

From: Temporal transcriptomic changes in the THY-Tau22 mouse model of tauopathy display cell type- and sex-specific differences

Cell Type

Sex-Specific Changes

Sex-Dimorphic Changes

Microglia

Malat1 (↑♂)

H2-D1 (↑♂)

Tyrobp (↑♂)

Hsp90ab1 (↑♀)

Cst3 (↑♂/↓♀)

Ccl3 (↑♂/↓♀)

Hsp90b1 (↓♂/↑♀)

Astrocytes

Clu (↑♂)

Cldn10 (↑♂)

Cpe (↑♂)

Pnisr (↑♀)

mt-Rnr2 (↑♂/↓♀)

Apoe (↑♂/↓♀)

Mt1 (↑♂/↓♀)

Neurons

mt-Cytb (↑♂)

Sparcl1 (↑♂)

Snhg11 (↑♂)

Strbp (↓♂)

Plp1 (↑♂/↓♀)

Atp1b1 (↓♂/↑♀)

mt-Rnr2 (↓♂/↑♀)

Oligodendrocytes

Car2 (↑♂)

mt-Nd1 (↑♂)

mt-Nd2 (↑♂)

Malat1 (↓♂/↑♀)

Fth1 (↑♂/↓♀)

Mbp (↑♂/↓♀)

Endothelial cells

Id3 (↑♂)

Cxcl12 (↓♀)

Eif3a (↓♂)

mt-Rnr2 (↓♂/↑♀)

B2m (↑♂/↓♀)

Malat1 (↓♂/↑♀)

  1. Summary of the most significant differentially expressed genes showing either sex-specific or sex-dimorphic patterns across five major brain cell types. Sex-specific changes indicate significant alterations (FDR < 0.05, absolute log2 fold-change ≥ 0.5) in one sex only (♂: male, ♀: female) with direction shown by arrows (↑: increased, ↓: decreased). Sex-dimorphic changes indicate significant opposing changes between sexes. Notable patterns include widespread male-specific upregulation across cell types, recurrent dysregulation of Malat1 across multiple cell populations, and cell type-specific regulation of genes involved in inflammation (microglia), protein homeostasis (astrocytes), mitochondrial function (neurons), myelination (oligodendrocytes), and vascular function (endothelial cells). All changes compare THY-Tau22 mice to wild-type controls