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Follicle-stimulating hormone stimulated differentiation and progesterone production of bovine granulosa cells in culture
Institution:1. Scottish Agricultural College, 581 King Street, School of Agriculture, Aberdeen AB9 1UD, UK;2. University of Aberdeen, 581 King Street, School of Agriculture, Aberdeen AB9 1UD, UK;1. Department of Laboratory Medicine, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China;2. First Clinical College, Fujian Medical University, Fuzhou, China;3. Fujian Key Laboratory of Laboratory Medicine, Fuzhou, China;1. Department of Biochemistry, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, Nijmegen, The Netherlands;2. CIQUP/Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, Portugal;1. Department of Theriogenology, Faculty of Veterinary Science, University of Veterinary and Animal Sciences, Lahore 54000, Pakistan;2. Nuclear Institute for Agriculture and Biology (NIAB), Faisalabad 38000, Pakistan;3. Department of Epidemiology and Public Health, Faculty of Veterinary Science, University of Veterinary and Animal Sciences, Lahore 54000, Pakistan;4. Department of Animal Sciences, University of Florida, Gainesville, FL 32611, USA
Abstract:Progesterone production of granulosa cells cultured in vitro is stimulated and cell differentiation increased, by follicle-stimulating hormone (FSH). This study examined whether the increased progesterone production observed when bovine granulosa cells are cultured occurs because (1) progesterone production by undifferentiated and/or differentiated cells is increased or (2) the differentiation of granulosa cells is stimulated. Viable bovine granulosa cells (2−3×105) from follicles 5–8 mm in diameter were cultured in the presence of 0, 1, 10 and 100 μu FSH (1 μu ≡ 1 μg NIH-FSH-S1) for 6 days at 37°C in a humidified atmosphere of 5% CO2 in air in 1 ml of a 1:1 mixture of Dulbecco's modified Eagle medium: Ham's F10 medium supplemented with 365 μg ml−1 l-glutamine, 100 U ml−1 penicillin and 100 μg ml−1 streptomycin. Progesterone production, total DNA and protein, and cell diameter were determined sequentially over the culture period. The increases in progesterone production (ng μg−1 DNA per 24 h), cytoplasmic:nuclear ratio (μg protein μg−1 DNA) and cell diameter (μm) over 6 days culture indicated that granulosa cells underwent differentiation in the presence of FSH. Progesterone production of undifferentiated granulosa cells (diameter 14 μm or less) was stimulated by FSH (P < 0.01) in a dose dependent manner (1.0±0.2, 2.9±0.3, 3.7±0.3 and 4.9±0.4 ng μg−1 DNA per 24 h for 0, 1, 10 and 100 μu ml−1 FSH respectively) but remained constant within dose (P > 0.05) during a 6 day culture period. FSH stimulated (P < 0.05) the rate of granulosa cell differentiation (10±3%, 53±13%, 74±21% and 82±10% differentiating cells per well for 0 μu, 1 μu, 10 μu and 100 μu ml−1 FSH respectively) but did not stimulate (P > 0.05) progesterone production by differentiating granulosa cells (8.7±0.5 ng μg−1 DNA per 24 h). In conclusion, the increase in progesterone production of FSH-stimulated granulosa cells cultured in vitro appears to be mainly due to an increase in the number of differentiating cells with a constant rather than an increasing progesterone production per cell.
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