Molecular mechanisms of enhancing porcine granulosa cell proliferation and function by treatment in vitro with anti-inhibin alpha subunit antibody
文献类型: 外文期刊
作者: Cai, Liuping 1 ; Sun, Aidong 1 ; Li, Hui 1 ; Tsinkgou, Anastasia 2 ; Yu, Jianning 1 ; Ying, Shijia 1 ; Chen, Zhe 1 ; Shi, 1 ;
作者机构: 1.Jiangsu Acad Agr Sci, Inst Anim Sci, Lab Anim Breeding & Reprod, Nanjing 210014, Jiangsu, Peoples R China
2.Xijiao Liverpool Univ, Dept Life Sci, Suzhou 215123, Peoples R China
关键词: Immunoneutralization of inhibin bioactivity;Porcine granulosa cells;Estradiol secretion;Proliferation;Molecular mechanisms
期刊名称:REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY ( 影响因子:5.211; 五年影响因子:5.017 )
ISSN: 1477-7827
年卷期: 2015 年 13 卷
页码:
收录情况: SCI
摘要: Background: This study was conducted to clarify the effect of the inhibiting action of inhibin on porcine granulosa cell proliferation and function, and to investigate the underlying intracellular regulatory molecular mechanisms. Methods: Porcine granulosa cells were cultured in vitro, and were treated with an anti-inhibin alpha subunit antibody, with or without co-treatment of follicle-stimulating hormone (FSH) in the culture medium. Results: Treatment with anti-inhibin alpha subunit antibody led to a significant increase in estradiol (E2) secretion and cell proliferation. Anti-inhibin alpha subunit antibody worked synergistically with FSH at low concentrations (25 microg/mL) to stimulate E2 secretion, but attenuated FSH action at high concentrations (50 microg/mL). Immunoneutralization of inhibin bioactivity increased FOXL2, Smad3, and PKA phosphorylation, and mRNA expression of the transcription factors CEBP and c-FOS. The expression of genes encoding gonadotropin receptors, FSHR and LHR, and of those involved in steroidogenesis, as well as IGFs and IGFBPs, the cell cycle progression factors cyclinD1 and cyclinD2, and the anti-apoptosis and anti-atresia factors Bcl2, TIMP, and ADAMTS were upregulated following anti-inhibin alpha-subunit treatment. Treatment with anti-inhibin alpha subunit down regulated expression of the pro-apoptotic gene encoding caspase3. Although expression of the pro-angiogenesis genes FN1, FGF2, and VEGF was upregulated, expression of the angiogenesis-inhibiting factor THBS1 was downregulated following anti-inhibin alpha subunit treatment. Conclusions: These results suggest that immunoneutralization of inhibin bioactivity, through augmentation of the activin and gonadotropin receptor signaling pathways and regulation of gene expression, permits the development of healthy and viable granulosa cells. These molecular mechanisms help to explain the enhanced ovarian follicular development observed following inhibin immunization in animal models.
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