Spatiotemporal dynamics of early oogenesis in pigs

In humans and other mammals, the process of oogenesis initiates asynchronously in specific ovarian regions, leading to the localization of dormant and growing follicles in the cortex and medulla, respectively; however, the current understanding of this process remains insufficient. Here, we integrat...

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Published inGenome Biology Vol. 26; no. 1; p. 2
Main Authors Ge, Wei, Niu, Yi-Lin, Li, Yu-Kang, Li, Li, Wang, Han, Li, Wen-Wen, Qiao, Tian, Feng, Yan-Ni, Feng, Yu-Qing, Liu, Jing, Wang, Jun-Jie, Sun, Xiao-Feng, Cheng, Shun-Feng, Li, Lan, Shen, Wei
Format Journal Article
LanguageEnglish
Published England BioMed Central 02.01.2025
BMC
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Summary:In humans and other mammals, the process of oogenesis initiates asynchronously in specific ovarian regions, leading to the localization of dormant and growing follicles in the cortex and medulla, respectively; however, the current understanding of this process remains insufficient. Here, we integrate single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics (ST) to comprehend spatial-temporal gene expression profiles and explore the spatial organization of ovarian microenvironments during early oogenesis in pigs. Projection of the germ cell clusters at different stages of oogenesis into the spatial atlas unveils a "cortical to medullary (C-M)" distribution of germ cells in the developing porcine ovaries. Cross-species analysis between pigs and humans unveils a conserved C-M distribution pattern of germ cells during oogenesis, highlighting the utility of pigs as valuable models for studying human oogenesis in a spatial context. RNA velocity analysis with ST identifies the molecular characteristics and spatial dynamics of granulosa cell lineages originating from the cortical and medullary regions in pig ovaries. Spatial co-occurrence analysis and intercellular communication analysis unveils a distinct cell-cell communication pattern between germ cells and somatic cells in the cortex and medulla regions. Notably, in vitro culture of ovarian tissues verifies that intercellular NOTCH signaling and extracellular matrix (ECM) proteins played crucial roles in initiating meiotic and oogenic programs, highlighting an underappreciated role of ovarian microenvironments in orchestrating germ cell fates. Overall, our work provides insight into the spatial characteristics of early oogenesis and the regulatory role of ovarian microenvironments in germ cell fate within a spatial context.
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ISSN:1474-760X
1474-7596
1474-760X
DOI:10.1186/s13059-024-03464-8