a Animal Biotechnology Department , Institute of Tropical Biology, Vietnam Academy of Science and Technology , Ho Chi Minh City , Vietnam.
b Biotechnology Department , Graduate University of Science and Technology, Vietnam Academy of Science and Technology , Ha Noi , Vietnam.
Cell Cycle. 2019 Jul;18(13):1490-1497. doi: 10.1080/15384101.2019.1624108. Epub 2019 May 31.
The objective of this study was to evaluate replicative senescence of bovine granulosa cells (bGCs) during long-term culture. WST-1 assay analysis showed that bGCs proliferation was reduced from primary culture to 14th passage. The several bGCs from the 3rd passage and 7th passage exposed the weak activity of beta-galactosidase, while a strongly positive staining of beta-galactosidase was observed in bGCs from 14th passage. Flow cytometry analysis showed that bGCs were induced to cell cycle arrest at G0/G1 phase through expansion. transcript expression of bGCs was downregulated from primary culture to 14th passage. The cell and nuclear area of bGCs were dramatically increased from 14th passage to 25th passage. The nucleocytoplasmic ratio of bGCs was dramatically reduced in 22th passage (4.32%) and 25th passage (2.45%), comparing to previous passages: primary culture (10.67%), 7th passage (9.21%), or 14th passage (10.33%). The number of microfilament bundle of bGCs was increased in 22nd passage (67.42 ± 17.76) and 25th passage (56.31 ± 22.45). The diameter of microfilament bundle of bGCs in 25th passage was dramatically increased to 1.88 ± 0.32 µm comparing to the primary culture (1.15 ± 0.03 µm). In this study, we also assessed the nuclear form factor which illustrates the level of nuclear circular form. A reduction of nuclear form factor was observed in bGCs during long-term expansion. The changes of nuclear form factor were correlated to other senescent characteristics, especially the nucleocytoplasmic ratio.
本研究旨在评估牛颗粒细胞(bGCs)在长期培养过程中的复制性衰老。WST-1 分析表明,bGCs 的增殖能力从原代培养到第 14 代时降低。第 3 代和第 7 代的几个 bGCs 表现出β-半乳糖苷酶活性较弱,而第 14 代的 bGCs 则表现出强烈的β-半乳糖苷酶染色阳性。流式细胞术分析表明,bGCs 通过扩增被诱导至 G0/G1 期细胞周期停滞。bGCs 的转录表达从原代培养到第 14 代时下调。从第 14 代到第 25 代,bGCs 的细胞和核面积显著增加。第 22 代(4.32%)和第 25 代(2.45%)的 bGCs 的核质比与前几代相比显著降低:原代培养(10.67%)、第 7 代(9.21%)或第 14 代(10.33%)。第 22 代(67.42±17.76)和第 25 代(56.31±22.45)的 bGCs 中的微丝束数量增加。第 25 代的 bGCs 微丝束直径与原代培养相比显著增加,达到 1.88±0.32 µm(1.15±0.03 µm)。在本研究中,我们还评估了核形态因子,该因子反映了核的圆形形态水平。在长期扩增过程中,bGCs 的核形态因子降低。核形态因子的变化与其他衰老特征相关,特别是核质比。