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鸭分级卵泡膜细胞培养模型的建立。

Establishment of an culture model of theca cells from hierarchical follicles in ducks.

作者信息

Gan Xiang, Chen Da, Deng Yan, Yuan Jusong, Kang Bo, Qiu Jiamin, Sun Wenqiang, Han Chunchun, Hu Jiwei, Li Liang, Wang Jiwen

机构信息

Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, ChengDu, SiChuan, China.

Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, ChengDu, SiChuan, China

出版信息

Biosci Rep. 2017 May 11;37(3). doi: 10.1042/BSR20160491. Print 2017 Jun 30.

Abstract

Theca cells, including theca interna cells and theca externa cells, are vital components of ovarian follicles. The aim of the present study is to identify a reliable method for the culture of theca cells from duck ovarian hierarchical (F4-F2) follicles. We improved the method for cell separation by using trypsin to further remove granular cells, and we increased the concentration of fetal bovine serum used in culture to improve cytoactivity. Cell antibody immunofluorescence (IF) showed that all inoculated cells could be stained by the CYP17A1/19A1 antibody but not by the FSHR antibody, which could stain granulosa cells. Furthermore, morphological differences were observed between the outlines of theca interna and externa cells and in their nuclei. Growth curve and mRNA relative expression analyses suggested that the growth profile of theca interna cells may have been significantly different from that of theca externa cells Theca interna cells experienced the logarithmic phase on d1-d2, the plateau phase on d2-d3, and the senescence phase after d3, while theca externa cells experienced the logarithmic phase on d1-d3, the plateau phase on d3-d5, and the senescence phase after d5. Taken together, these results suggested that we have successfully established a reliable theca cell culture model and further defined theca cell characteristics .

摘要

卵泡膜细胞,包括卵泡膜内层细胞和卵泡膜外层细胞,是卵巢卵泡的重要组成部分。本研究的目的是确定一种可靠的方法,用于培养鸭卵巢分级(F4 - F2)卵泡的卵泡膜细胞。我们改进了细胞分离方法,使用胰蛋白酶进一步去除颗粒细胞,并提高了培养中使用的胎牛血清浓度以提高细胞活性。细胞抗体免疫荧光(IF)显示,所有接种的细胞都可以被CYP17A1/19A1抗体染色,但不能被可染色颗粒细胞的FSHR抗体染色。此外,在卵泡膜内层和外层细胞的轮廓及其细胞核中观察到形态差异。生长曲线和mRNA相对表达分析表明,卵泡膜内层细胞的生长曲线可能与卵泡膜外层细胞有显著差异。卵泡膜内层细胞在第1 - 2天经历对数期,第2 - 3天经历平台期,第3天后进入衰老期,而卵泡膜外层细胞在第1 - 3天经历对数期,第3 - 5天经历平台期,第5天后进入衰老期。综上所述,这些结果表明我们已成功建立了一种可靠的卵泡膜细胞培养模型,并进一步明确了卵泡膜细胞的特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9c3/5426285/c8092e90d280/BSR-2016-0491i001.jpg

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