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AbstractHuman fetal adrenal glands produce substantial amounts of dehydroepiandrosterone (DHEA), which is one of the most important precursors of sex hormones. However, the underlying biological mechanism remains largely unknown. Herein, we sequenced human fetal adrenal glands and gonads from 7 to 14 GW via the 10× Genomics single-cell transcriptome techniques and reconstructed their location information by Spatial Transcriptome, conducted COOL-seq for the MC2R+ inner zone steroidogenic cells during the time window of sex differentiation (8-12GW). We found that relative to gonads, adrenal glands begin to synthesize steroids early. The coordination among steroidogenic cells and multiple nonsteroidogenic cells promotes adrenal cortex construction and steroid synthesis. Notably, during the time window of sex differentiation (8–12 GW), key enzyme gene expression shifts to accelerate DHEA synthesis in males and cortisol synthesis in females. Furthermore, high SST+ expressions in the adrenal gland and testis amplify androgen synthesis in males. Our research highlights the robustness of the action of fetal adrenal glands on gonads to modify the process of sexual differentiation.
Male, adrenal glands, Sex Differentiation, spatial transcriptomics, sexual differentiation, Dehydroepiandrosterone, RC648-665, Diseases of the endocrine glands. Clinical endocrinology, Endocrinology, Fetus, Adrenal Glands, Humans, Female, Sc-RNA sequencing, steroidogenic regulation network, Gonads
Male, adrenal glands, Sex Differentiation, spatial transcriptomics, sexual differentiation, Dehydroepiandrosterone, RC648-665, Diseases of the endocrine glands. Clinical endocrinology, Endocrinology, Fetus, Adrenal Glands, Humans, Female, Sc-RNA sequencing, steroidogenic regulation network, Gonads
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