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GPK细胞培养物增殖率的克隆变异。

Clonal variation in proliferation rate of cultures of GPK cells.

作者信息

Riley P A, Hola M

出版信息

Cell Tissue Kinet. 1981 Sep;14(5):489-99. doi: 10.1111/j.1365-2184.1981.tb00555.x.

Abstract

Pedigrees of twenty-six clones of a line of keratocytes derived from guinea-pig ear epidermis (GPK cells) were analysed from time-lapse film. The mean interdivision time (IDT) for the culture was 1143 +/- 215 (SD) min. The mean generation rates (mean reciprocal interdivision times) of clones varied over a range of 3.93--10.2 x 10(-4)/min and the standard deviation of the clonal mean generation rates was 16.8% of the average value. Transient intraclonal variations in IDT due to mitoses in a plane perpendicular to the substratum were observed. The data were also analysed on the basis of cell location in sixteen equal zones (quadrats) of the filmed area. The mean generation rate of quadrats was 8.73 x 10(-4)/min (SD = 4.9%). The spatial distribution showed some clustering of cells. The mean local density of the clones (2.25 +/- 0.62 cells/10(-4) cm2) was significantly higher than the quadrat density (1.76 +/- 0.8 cells/10(-4) cm2). There was no significant correlation between clonal density and mean generation rates, whereas for quadrats a significant negative correlation was found (P = 2.7%). The results support the proposition that cell lineage is the major determinant of the proliferation rate of subconfluent cultures.

摘要

从延时拍摄影片中分析了源自豚鼠耳表皮的角质形成细胞系(GPK细胞)的26个克隆的谱系。该培养物的平均分裂间期(IDT)为1143±215(标准差)分钟。克隆的平均生成率(平均倒数分裂间期)在3.93 - 10.2×10⁻⁴/分钟范围内变化,克隆平均生成率的标准差为平均值的16.8%。观察到由于在垂直于基质的平面内进行有丝分裂而导致的克隆内IDT的瞬时变化。还根据拍摄区域的16个相等区域(样方)中的细胞位置对数据进行了分析。样方的平均生成率为8.73×10⁻⁴/分钟(标准差 = 4.9%)。空间分布显示细胞有一些聚集。克隆的平均局部密度(2.25±0.62个细胞/10⁻⁴平方厘米)显著高于样方密度(1.76±0.8个细胞/10⁻⁴平方厘米)。克隆密度与平均生成率之间没有显著相关性,而对于样方则发现有显著的负相关(P = 2.7%)。结果支持细胞谱系是亚汇合培养物增殖率的主要决定因素这一观点。

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