Simulated microgravity altered the cell cycle progression of porcine granulosa cells

Truong Xuan Dai, Hoang Nghia Son, Le Thanh Long
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Abstract

Microgravity has been shown to markedly affect reproduction in humans and animals, especially reproductive organs such as the ovaries. Granulosa cells are one of the important components of the ovary, playing an important role in supporting oocyte maturation and fertilization. However, the effects of microgravity on granulosa cells have not been well characterized. This study aimed to assess the effects of simulated microgravity (SMG) on the cell cycle progression of porcine granulosa cells (pGCs). The pGCs were induced SMG for 72 h by Gravite® simulator, while cells of the control group were treated in normal conditions. Cell cycle analysis revealed that SMG condition induced an increase of the ratio of pGCs in the G0/G1 phase, leading to the cell cycle arrest phase, while the ratio of pGCs in the G2/M phase was decreased. There was no difference in the cell ratio of the S phase between the control group and the SMG group. Real-time RT-PCR analysis indicated that the expression of cdk4 and cdk6 transcripts of pGCs from the SMG group was lower than the control group. This down-regulation was also observed cyclin A and cyclin D1 transcript expression in pGCs from the SMG group. Immunostaining displayed the lower exhibition of microfilament and microtubule in pGCs from the SMG group comparing to the control group. Western blot analysis showed that the expression of β-actin and α-tubulin was reduced in pGCs from the SMG group. These changes contributed to the alteration of cytoskeletal structure, including microfilaments and microtubules, which affect cell division. These results revealed that the SMG condition induced changes in the cell cycle progression of pGCs. 
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模拟微重力改变了猪颗粒细胞的细胞周期进程
微重力已被证明会显著影响人类和动物的生殖,特别是生殖器官,如卵巢。颗粒细胞是卵巢的重要组成部分之一,在支持卵母细胞成熟和受精方面起着重要作用。然而,微重力对颗粒细胞的影响尚未被很好地表征。本研究旨在评估模拟微重力(SMG)对猪颗粒细胞(pGCs)细胞周期进程的影响。采用Gravite®模拟器诱导pGCs SMG 72 h,对照组细胞在正常条件下处理。细胞周期分析显示,SMG诱导G0/G1期pGCs的比例增加,导致细胞周期停滞期,而G2/M期pGCs的比例减少。对照组与SMG组S期细胞比例无明显差异。Real-time RT-PCR分析显示,SMG组pGCs中cdk4和cdk6转录本的表达低于对照组。在SMG组的pGCs中也观察到细胞周期蛋白A和细胞周期蛋白D1转录本表达的下调。免疫染色显示,与对照组相比,SMG组pGCs中微丝和微管的表现较低。Western blot分析显示,SMG组pGCs中β-actin和α-tubulin的表达降低。这些变化导致细胞骨架结构的改变,包括微丝和微管,从而影响细胞分裂。这些结果表明,SMG条件诱导了pGCs细胞周期进程的变化。
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