卵泡期
间充质干细胞
男科
毛囊
骨髓
生物
谷胱甘肽
卵巢皮质
卵母细胞
内分泌学
化学
内科学
卵巢
免疫学
医学
胚胎
生物化学
细胞生物学
卵巢组织
酶
作者
Camila Arrivabene Neves,Lucilene dos Santos Silva,Camila Ernanda Sousa de Carvalho,Marina Silva Carvalho,José Lindenberg Rocha Sarmento,Tânia Vasconcelos Cavalcante,Mônica Arrivabene,Tábatta Arrivabene Neves,Maria Éllida de Sousa Bezerra,Antônio Luíz Gomes Júnior,Cleidson Manoel Gomes da Silva,Maria Acelina Martins de Carvalho
出处
期刊:Zygote
[Cambridge University Press]
日期:2019-11-18
卷期号:28 (1): 65-71
被引量:9
标识
DOI:10.1017/s0967199419000686
摘要
This study aims to develop an in vitro co-culture system of in situ goat preantral follicles with bone marrow-derived mesenchymal stem cells (BM-MSC), evaluating the influence of these cells on follicular growth, rate of activation and morphologically normal follicles. Fragments of ovarian cortex were cultured for 1 or 7 days in the presence of BM-MSC (BM-MSC+) and absence of BM-MSC (BM-MSC-). Histological sections of the fragments were analysed and data were obtained regarding morphological classification, survival rate of morphologically normal follicles and rate of follicular activation. Culture medium on days 1 and 7 was also sampled for nitrite concentration and reduced glutathione activity. There was a reduction (P < 0.05) in the percentage of morphologically normal follicles in the BM-MSC+ compared with the fresh control only on the seventh day of culture. When comparing treatments, on the seventh day of culture, a higher rate of morphologically normal preantral follicles was observed in BM-MSC+ (P < 0.05). In both treatments, primordial and developing follicle rates were similar to the fresh control (P > 0.05). When comparing treatments with each other, as well as with the fresh control, no differences were observed in follicular diameter (P > 0.05) or nitrite concentration (P > 0.05). The concentration of reduced glutathione was lower on the seventh day of co-culture in both treatments (P < 0.05). In conclusion, co-culture had no influence on follicular or oocyte development. However, it was critical to maintain the survival of preantral follicles during 7 days of culture.
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