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Effects of fibroblast growth factor-2 on the in vitro culture of caprine preantral follicles.

机译:成纤维细胞生长因子2对山羊腔前卵泡体外培养的影响。

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The aims of the present study were to evaluate the effects of fibroblast growth factor-2 (FGF-2) on survival, activation and growth of caprine early-staged (preantral) follicles using histological and ultrastructural studies. Fragments of caprine ovarian cortex were cultured for 1 or 5 days in an enriched minimum essential medium, supplemented or not with different concentrations of FGF-2 (10, 50 or 100 ng/ml). Fragments from non-cultured ovarian tissue (control) and from tissues cultured for 1 or 5 days in a specific medium were processed for transmission electron microscopy (TEM) or classical histology to evaluate the morphological quality of caprine preantral follicles and to calculate the percentages of normal follicles. Additionally, effects of FGF-2 on oocyte and follicle diameter of cultured preantral follicles were investigated. Our results showed that, although the percentages of histologically normal follicles were lower in cultured than in non-cultured ovarian tissue fragments, there were nodifferences in this regard among treatments, neither on day 1 nor on day 5 of culture. After 1 and 5 days of culture, a significantly higher percentage of growing follicles was observed in the medium supplemented with 50 ng/ml of FGF-2. This FGF-2 treatment furthermore resulted in an increase in diameter of both oocytes and follicles that were cultured for 5 days. TEM showed that the ultrastructural integrity of caprine preantral follicles was maintained during their 5-day culture in the presence of 50 ng/ml FGF-2. In conclusion, this study demonstrated that at a concentration of 50 ng/ml FGF-2 not only maintains the morphological integrity of caprine preantral follicles cultured for 5 days, but also stimulates the activation of primordial follicles and the growth of activated follicles.
机译:本研究的目的是使用组织学和超微结构研究来评估成纤维细胞生长因子2(FGF-2)对山羊早期(窦前)卵泡存活,激活和生长的影响。在丰富的基本必需培养基中补充或不添加不同浓度的FGF-2(10、50或100 ng / ml),将山羊卵巢皮质的片段培养1或5天。将未培养的卵巢组织(对照)和在特定培养基中培养1或5天的组织的片段进行透射电子显微镜(TEM)或经典组织学处理,以评估山羊窦前卵泡的形态学质量并计算百分比正常卵泡。另外,研究了FGF-2对培养的腔前卵泡的卵母细胞和卵泡直径的影响。我们的结果表明,尽管培养的组织学正常卵泡百分比低于未培养的卵巢组织碎片,但在处理的这方面,在培养的第1天和第5天都没有差异。培养1天和5天后,在添加了50 ng / ml FGF-2的培养基中观察到明显更高的卵泡生长百分比。该FGF-2处理还导致培养5天的卵母细胞和卵泡直径的增加。 TEM显示,在存在50 ng / ml FGF-2的情况下培养5天时,山羊窦前卵泡的超微结构完整性得以保持。总之,这项研究表明,浓度为50 ng / ml的FGF-2不仅可以维持培养5天的山羊窦前卵泡的形态完整性,而且还可以刺激原始卵泡的活化和活化卵泡的生长。

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