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[Fas/FasL在体外培养过程中对分离卵泡来源的猪卵泡颗粒细胞凋亡的作用]

[Role of Fas/FasL on apoptosis of porcine follicular granulosa cells derived from isolated follicles during culture in vitro].

作者信息

Lin Peng-Fei, Hao Yuan-Bing, Guo Hui-Li, Liu Hong-Lin, Rui Rong

机构信息

College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.

出版信息

Dongwuxue Yanjiu. 2010 Jun;31(3):268-74. doi: 10.3724/SP.J.1141.2010.03268.

Abstract

The whole antral follicles were isolated from porcine ovaries and classified as follows: healthy follicles (HF), early atretic follicles (EF) and progressed atretic follicles (PF). The isolated porcine follicles were used for routine histological section and HE staining after examination by eyesight. Morphological research shows that the accuracy rate of eyesight examination for HF is 92%. Healthy follicles were chosen for further experiment and divided into 3 groups: large follicles (greater than 5 mm in diameter), medium follicles (3-5 mm in diameter) and small follicles (less than 3 mm in diameter). All follicles were cultured for 8, 16 and 24 h, respectively and the apoptosis of of their granulosa cells were examined by Annexin V-FITC/PI double-labeling. It showed that the total apoptotic rate of granulosa cells derived from cultured follicles could reach over 70% at 8 h after culture and be 81.1% - 94.6% at 24 h after culture. Granulosa cells from groups were collected at 0, 8, 16, 24, 48 and 72 h after culture without serum and used for the examination of expression of FasL and Fas mRNA with real time PCR SYBRgreen method. The expression level of FasL mRNA of granulosa cells from different size of follicles increased with culture time and reached the highest level at 24 h after culture (P<0.05). Expression level of FasL mRNA of granulosa cells from small follicles was higher than those from large and medium follicles. There exists no difference for expression level of Fas mRNA of granulosa cells among groups before culture but significantly increased at 8 h after culture and reached the highest level at 48 h after culture. It showed in the present experiment that the follicular culture system without serum used could effectively induce the apoptosis of follicular granulosa cells. Cell apoptosis is the main cause of follicular atresia, the degree of which varied with the size of follicles. Small follicles seemed to be easier atretic than medium and large follicles.

摘要

从猪卵巢中分离出整个窦状卵泡,并将其分为以下几类:健康卵泡(HF)、早期闭锁卵泡(EF)和进展期闭锁卵泡(PF)。分离出的猪卵泡经肉眼检查后用于常规组织切片和苏木精-伊红(HE)染色。形态学研究表明,肉眼检查HF的准确率为92%。选择健康卵泡进行进一步实验,并将其分为3组:大卵泡(直径大于5mm)、中卵泡(直径3-5mm)和小卵泡(直径小于3mm)。所有卵泡分别培养8、16和24小时,并用膜联蛋白V-异硫氰酸荧光素/碘化丙啶(Annexin V-FITC/PI)双标记法检测其颗粒细胞的凋亡情况。结果显示,培养卵泡来源的颗粒细胞总凋亡率在培养8小时后可达70%以上,在培养24小时后为81.1%-94.6%。培养后0、8、16、24、48和72小时,在无血清条件下收集各组颗粒细胞,采用实时荧光定量PCR SYBRgreen法检测FasL和Fas mRNA的表达。不同大小卵泡颗粒细胞FasL mRNA表达水平随培养时间增加而升高,在培养24小时达到最高水平(P<0.05)。小卵泡颗粒细胞FasL mRNA表达水平高于大、中卵泡。培养前各组颗粒细胞Fas mRNA表达水平无差异,但在培养8小时后显著升高,在培养48小时达到最高水平。本实验表明,所采用的无血清卵泡培养系统可有效诱导卵泡颗粒细胞凋亡。细胞凋亡是卵泡闭锁的主要原因,其程度随卵泡大小而异。小卵泡似乎比中、大卵泡更容易闭锁。

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