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首页> 外文期刊>Reproduction, fertility, and development >Effects of growth differentiation factor-9 and FSH on in vitro development, viability and mRNA expression in bovine preantral follicles
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Effects of growth differentiation factor-9 and FSH on in vitro development, viability and mRNA expression in bovine preantral follicles

机译:生长分化因子-9和FSH对牛预血管卵泡体外发育,活力和mRNA表达的影响

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摘要

The present study investigated the role of growth differentiation factor (GDF)-9 and FSH, alone or in combination, on the growth, viability and mRNA expression of FSH receptor, proliferating cell nuclear antigen (PCNA) and proteoglycan-related factors (i.e. hyaluronan synthase (HAS) 1, HAS2, versican, perlecan) in bovine secondary follicles before and after in vitro culture. After 12 days culture, sequential FSH (100ngmL-1 from Days 0 to 6 and 500ngmL-1 from Days 7 to 12) increased follicular diameter and resulted in increased antrum formation (P0.05). Alone, 200ngmL-1 GDF-9 significantly reduced HAS1 mRNA levels, but increased versican and perlecan mRNA levels in whole follicles, which included the oocyte, theca and granulosa cells. Together, FSH and GDF-9 increased HAS2 and versican (VCAN) mRNA levels, but decreased PCNA mRNA expression, compared with levels in follicles cultured in α-minimum essential medium supplemented with 3.0mgmL -1 bovine serum albumin, 10μgmL-1 insulin, 5.5μgmL-1 transferrin, 5ngmL-1 selenium, 2mM glutamine, 2mM hypoxanthine and 50gmL-1 ascorbic acid (α-MEM+). Comparisons of uncultured (0.2mm) and α-MEM+ cultured follicles revealed that HAS1 mRNA expression was higher, whereas VCAN expression was lower, in cultured follicles (P0.05). Expression of HAS1, VCAN and perlecan (HSPG2) was higher in cultured than in vivo-grown (0.3mm) follicles. In conclusion, FSH and/or GDF-9 promote follicular growth and antrum formation. Moreover, GDF-9 stimulates expression of versican and perlecan and interacts positively with FSH to increase HAS2 expression.
机译:本研究研究了生长分化因子(GDF)-9和FSH,单独或组合的作用对FSH受体的生长,活力和mRNA表达,增殖细胞核抗原(PCNA)和蛋白多糖相关因素(即Hyaluronan在体外培养之前和之后,在牛二次卵泡中合成(具有)1,Hase2,Versican,Percecan)。 12天培养后,顺序FSH(100ngml-1从0至6天和500ngml -1,从第7至12天开始)增加卵泡直径,导致胃窦形成增加(P <0.05)。单独,200ngml-1 gdf-9显着降低了Hase1 mRNA水平,但是整个卵泡中的百分之百和Percecan mRNA水平增加,其中包括卵母细胞,Theca和颗粒细胞。 COME,FSH和GDF-9增加了HARS2和VERICAN(VCAN)mRNA水平,但是降低了PCNA mRNA表达,与在α-最低基本培养基中培养的卵泡水平相比,其补充有3.0mgml -1牛血清白蛋白,10μgml-1胰岛素, 5.5μgml-1转铁蛋白,5ngml-1硒,2mm谷氨酰胺,2mm缺氧胺和50gml -1抗坏血酸(α-mem +)。未培养的(0.2mm)和α-MEM +培养卵泡的比较显示HAS1 mRNA表达较高,而VCAN表达较低,培养卵泡(P <0.05)。培养的表达,VCAN和PERCECAN(HSPG2)培养比体内生长(0.3mm)卵泡更高。总之,FSH和/或GDF-9促进滤泡生长和胃窦形成。此外,GDF-9刺激了Versican和Percecan的表达,并用FSH正面相互作用以增加Hase2表达。

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  • 作者单位

    Biotechnology Nucleus of Sobral (NUBIS) Federal University of Ceara CEP 62042-280 Sobral CE;

    Biotechnology Nucleus of Sobral (NUBIS) Federal University of Ceara CEP 62042-280 Sobral CE;

    Biotechnology Nucleus of Sobral (NUBIS) Federal University of Ceara CEP 62042-280 Sobral CE;

    Biotechnology Nucleus of Sobral (NUBIS) Federal University of Ceara CEP 62042-280 Sobral CE;

    Biotechnology Nucleus of Sobral (NUBIS) Federal University of Ceara CEP 62042-280 Sobral CE;

    Biotechnology Nucleus of Sobral (NUBIS) Federal University of Ceara CEP 62042-280 Sobral CE;

    Biotechnology Nucleus of Sobral (NUBIS) Federal University of Ceara CEP 62042-280 Sobral CE;

    LAMOFOPA Faculty of Veterinary Medicine State University of Ceara CEP 60740-000 Fortaleza CE;

    LAMOFOPA Faculty of Veterinary Medicine State University of Ceara CEP 60740-000 Fortaleza CE;

    LAMOFOPA Faculty of Veterinary Medicine State University of Ceara CEP 60740-000 Fortaleza CE;

    LAMOFOPA Faculty of Veterinary Medicine State University of Ceara CEP 60740-000 Fortaleza CE;

    Department of Pathobiology Faculty of Veterinary Medicine Utrecht University PO Box 80.163;

    Biotechnology Nucleus of Sobral (NUBIS) Federal University of Ceara CEP 62042-280 Sobral CE;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 产科学;
  • 关键词

    culture;

    机译:文化;

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