<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE312nnn/GSE312015/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Mus musculus</species><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE312015</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Single-cell spatial transcriptomics reveals sex-dependent gene expression and intercellular signaling in the mouse adrenal cortex</name><description>Sexual dimorphism profoundly influences adrenal physiology and disease susceptibility, yet its molecular and spatial basis remains poorly understood. The female-predominant X-zone, a transient cortical structure recognized for nearly a century, has lacked comprehensive molecular characterization. Here we use high-resolution Visium HD spatial transcriptomics with Cellpose-based cell segmentation to generate ~203,000 near-single-cell-resolution transcriptomic profiles from sexually mature mouse adrenal glands (four male, four female). We identify ten distinct cell populations with sex differences spatially restricted to inner cortical zones. The X-zone exhibits pronounced sexual dimorphism, with Akr1c18 (20α-hydroxysteroid dehydrogenase) as the definitive marker (log₂FC = −16.28, female-enriched), establishing the X-zone as a specialized progesterone-catabolizing endocrine compartment. Female adrenal glands exhibit greater intercellular communication complexity (435 vs 369 interactions) and higher aggregate signalling strength, with SPP1-integrin pathways enriched in the female X-zone microenvironment. Spatial trajectory inference reveals a dominant centripetal transcriptional gradient from the CT capsule toward the middle zona fasciculata conserved across both sexes, and a secondary centrifugal axis emanating from the JMZ/X region that is prominent in females and reflects the transcriptionally active X-zone. This spatial atlas establishes spatial restriction as a fundamental organizing principle of endocrine sexual dimorphism and provides a foundational resource for investigating sex-specific adrenal physiology, with implications for precision medicine approaches to adrenal disorders.</description><dates><publication>2026/06/25</publication></dates><accession>GSE312015</accession><cross_references><GSM>GSM9336190</GSM><GSM>GSM9336189</GSM><GPL>34290</GPL><GSE>312015</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>