We have previously shown that TGFB1 inhibits estradiol (E-2) and progesterone (P-4) biosynthesis in FSH-stimulated bovine granulosa cells by selective inhibition of steroidogenic enzymes. The objective of this study was to assess the effects of TGFB1 on E2 and P4 steroidogenesis in bovine granulosa cells cultured in the absence of FSH and to measure the effects of TGFB1 on cell proliferation and apoptosis in the presence and absence of FSH. Bovine granulosa cells from 2 to 5 mm follicles were cultured in serum-free medium for 2-6 days. In the absence of FSH, the secretion Of P4 increased with time in culture (P<0.05). Addition of TGFB1 for 6 days decreased P4 secretion and mRNA levels of the P4 synthesis-associated genes STAR, CYP11A1, HSD3B1, and GSTA (P<0.05). In the absence of FSH, the secretion of E2 decreased and addition of TGFB1 for 6 days partially reversed this decline and stimulated E2 biosynthesis, CYP19A1 and HSD17B1 mRNA levels and CYP19A1 activity (P<0.05). Conversely, TGFB1 did not affect HSD17B7 expression and HSD17B-reducing activity. TGFBI decreased the proportion of cells in the G0/G1 and S+G2/M phases in FSH-stimulated and unstimulated granulosa cells (P<0.05). Furthermore, in the presence or absence of FSH, TGFB1 increased the proportion of cells in apoptosis measured by propidium iodide staining and flow cytometry and confirmed by increased levels of cleaved caspase-3 (P<0.05). Our results therefore indicate that TGFB1 inhibits luteinization in cultured bovine granulosa cells while maintaining an estrogenic phenotype, and this effect was associated with increased apoptosis. Reproduction (2009) 137 969-977
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Univ Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, JapanUniv Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
Arase, Mayu
Horiguchi, Kana
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Univ Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, JapanUniv Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
Horiguchi, Kana
Ehata, Shogo
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Univ Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, JapanUniv Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
Ehata, Shogo
Morikawa, Masato
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Uppsala Univ, Ludwig Inst Canc Res, Sci Life Lab, Uppsala, SwedenUniv Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
Morikawa, Masato
Tsutsumi, Shuichi
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Univ Tokyo, Res Ctr Adv Sci & Technol, Genome Sci Div, Tokyo, JapanUniv Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
Tsutsumi, Shuichi
Aburatani, Hiroyuki
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Univ Tokyo, Res Ctr Adv Sci & Technol, Genome Sci Div, Tokyo, JapanUniv Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
Aburatani, Hiroyuki
Miyazono, Kohei
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Univ Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
Uppsala Univ, Ludwig Inst Canc Res, Sci Life Lab, Uppsala, SwedenUniv Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
Miyazono, Kohei
Koinuma, Daizo
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Univ Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, JapanUniv Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan