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Studies of the cell cycle of in vitro cultured skin fibroblasts in goats: work in progress

机译:山羊体外培养皮肤成纤维细胞的细胞周期研究:正在进行中

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The effect of serum starvation and olomoucine treatment on the cell cycle and apoptosis of goat skin fibroblasts cultured in vitro is reported in this paper. The cells were obtained from the ear of a female goat 1.5 years of age. Analysis of cell cycle distribution by fluorescence-activated cell sorting (FACS) showed that 3.4, 60.8 and 15.1% of normally cycling cells were at G1, G0 and S phase, respectively. Serum starvation for 1, 3 and 5 days arrested 70.1, 70.2 and 83.4% cells, respectively, at G0/G1 phase. Seventy-eight percent of confluent cells were at G0/G1 stage, but in contrast to the serum starved group, this high percentage of G0/G1 cells was mainly associated with G1 cells. Of cells not deprived of serum, 73.6% were arrested at G1/G0 when treated with 100 muM olomoucine for 9 h compared to 85.5% of cells that had been starved of serum for 2 days (co-inhibition) (P < 0.01). After co-inhibition, 45% of cells entered S phase when re-cultured in normal medium for 5 h, indicating that the inhibition was reversible. Under normal culture conditions, 1.2% of cells underwent apoptosis. Serum starvation for 1, 2, 3, 5 and 10 days caused apoptosis in 1.7, 3.9, 4.5, 11.7 and 90.3% of cells, respectively. Treatment with 100 muM olomoucine for 9 h did not increase the number of apoptotic cells significantly (1.9%, P > 0.05). When cells were co-inhibited, 4.1 % of cells underwent apoptosis. In conclusion, although serum withdrawal for 5 days or more effectively arrested cells at G0/G1 stages, it increased apoptosis of cells significantly. However, co-inhibition by serum withdrawal and olomoucine treatment was found to be an appropriate treatment to obtain more healthy G0/G1 cells based on the low percentage of apoptotic cells after treatment.
机译:本文报道了血清饥饿和olomoucine处理对体外培养的山羊皮肤成纤维细胞的细胞周期和凋亡的影响。这些细胞是从1.5岁的雌性山羊的耳朵中获得的。通过荧光激活细胞分选术(FACS)分析细胞周期分布,发现正常循环细胞的3.4%,60.8%和15.1%分别处于G1,G0和S期。在G0 / G1期,血清饥饿1、3和5天分别使70.1、70.2和83.4%的细胞停滞。 78%的融合细胞处于G0 / G1阶段,但是与血清饥饿的组相比,G0 / G1细胞的这一高百分比主要与G1细胞有关。在未剥夺血清的细胞中,当用100μMolomoucine处理9 h时,有73.6%的细胞被阻滞在G1 / G0处,相比之下,饥饿2天(共抑制)的细胞中有85.5%的细胞被阻滞(P <0.01)。共抑制后,当在正常培养基中再培养5 h时,有45%的细胞进入S期,表明该抑制是可逆的。在正常培养条件下,有1.2%的细胞发生凋亡。血清饥饿1、2、3、5和10天分别导致1.7、3.9、4.5、11.7和90.3%的细胞凋亡。用100μMolomoucine处理9 h并未显着增加凋亡细胞的数量(1.9%,P> 0.05)。当细胞被共同抑制时,有4.1%的细胞发生凋亡。总之,尽管停药5天或更长时间可以有效地将细胞停滞在G0 / G1期,但它可以显着增加细胞凋亡。然而,由于治疗后凋亡细胞的百分比较低,因此发现通过血清停药和olomoucine处理共同抑制是获得更健康的G0 / G1细胞的合适方法。

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