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Updated: Jun 25, 2025

Separation of Avian Preovulatory Follicle Granulosa and Theca Cell Layers for Downstream Applications
Published on: October 25, 2024
DUSP8-attenuated ERK1/2 signaling mediates lipogenesis and steroidogenesis in chicken granulosa cells
Hao Sun1, Zhongzhen Lin1, Yanrong Gong1
1State Key Laboratory of Swine and Poultry Breeding Industry, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, China; Key Laboratory of Livestock and Poultry Multi-omics, Ministry of Agriculture and Rural Affairs, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu, China; Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu, China.
Abstract:
The lipogenesis and steroidogenesis of granulosa cells are crucial during follicular development, yet it remains unclear whether dual-specificity phosphatase 8 (DUSP8) is involved. In this study, the specific role of DUSP8 in lipogenesis and steroidogenesis was investigated through culturing chicken granulosa cells in vitro. The results revealed that the expression levels of adipogenic genes were elevated after DUSP8 overexpression and reduced after knockdown. The same was observed for lipid deposition in granulosa cells. Meanwhile, the steroidogenic gene expression and progesterone synthesis were promoted after DUSP8 overexpression and inhibited after knockdown. In addition, we also found that DUSP8 blocked the phosphorylation of extracellular regulatory kinase 1/2 (ERK1/2). Based on the previous results that activated ERK1/2 signaling inhibited lipid deposition and progesterone synthesis in chicken granulosa cells, we demonstrated that DUSP8 promoted lipid deposition and progesterone synthesis through mediating the ERK1/2 signaling pathway. The results will improve our understanding of the molecular regulatory mechanisms regarding lipid metabolism and progesterone synthesis in chicken granulosa cells.
Insights
Dual-specificity phosphatase 8 (DUSP8) promotes lipid deposition and progesterone synthesis in chicken granulosa cells. DUSP8 regulates these processes by influencing the extracellular signal-regulated kinase 1/2 (ERK1/2) signaling pathway.
Area of Science:
- Reproductive Biology
- Cellular Metabolism
- Molecular Endocrinology
Background:
- Granulosa cell lipogenesis and steroidogenesis are vital for follicular development.
- The precise role of dual-specificity phosphatase 8 (DUSP8) in these processes is not well understood.
- Investigating DUSP8's function can elucidate key regulatory mechanisms in avian reproduction.
Purpose of the Study:
- To determine the specific role of DUSP8 in regulating lipogenesis and steroidogenesis in chicken granulosa cells.
- To investigate the molecular pathway through which DUSP8 exerts its effects.
- To enhance understanding of lipid metabolism and progesterone synthesis during follicular development.
Main Methods:
- Primary chicken granulosa cells were cultured in vitro.
- DUSP8 was overexpressed and knocked down to assess its functional impact.
- Gene expression of adipogenic and steroidogenic markers was quantified.
- Lipid deposition and progesterone synthesis were measured.
- Extracellular signal-regulated kinase 1/2 (ERK1/2) phosphorylation was analyzed.
Main Results:
- DUSP8 overexpression increased adipogenic gene expression and lipid deposition.
- DUSP8 knockdown reduced adipogenic gene expression and lipid deposition.
- DUSP8 overexpression enhanced steroidogenic gene expression and progesterone synthesis.
- DUSP8 knockdown inhibited steroidogenic gene expression and progesterone synthesis.
- DUSP8 was found to inhibit ERK1/2 phosphorylation.
Conclusions:
- DUSP8 plays a significant role in promoting both lipogenesis and steroidogenesis in chicken granulosa cells.
- DUSP8 mediates these effects via the extracellular signal-regulated kinase 1/2 (ERK1/2) signaling pathway.
- These findings provide novel insights into the molecular regulation of lipid metabolism and progesterone production in avian granulosa cells.
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