兔关节软骨细胞原代培养和第一代增殖动力学。

Cell and tissue kinetics Pub Date : 1983-11-01
X Ronot, C Hecquet, P Jaffray, M Guiguet, M Adolphe, J Fontagne, P Lechat
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引用次数: 0

摘要

比较了幼兔关节软骨细胞原代培养和一次传代时的体外增殖动力学。用流动微荧光法测定两组细胞生长7 d期间的生长曲线标记和有丝分裂指数、百分比标记有丝分裂(PLM)曲线和DNA含量分布。由生长曲线指数部分计算的细胞周期长度和倍增时间非常相似:原代培养Tc = 19小时,Td = 20小时,第一代培养Tc = 17 × 3小时,Td = 20小时。但7 d内的生长曲线和DNA分布存在一定差异。生长曲线研究的滞后时间在原代培养中比在第一次传代中更长。FCM分析也观察到这一现象。培养第2天的生长分数测定与原代培养细胞增殖能力较低一致。这些数据表明,在第一次传代时研究关节软骨细胞的生长动力学和药物修饰比在原代培养中更好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proliferation kinetics of rabbit articular chondrocytes in primary culture and at the first passage.

The in-vitro proliferation kinetics of young rabbit articular chondrocytes were compared in primary culture and at the first passage. The growth curves labelling and mitotic indices, percentage labelled mitosis (PLM) curves and DNA content distributions by flow-microfluorometric analysis during a 7-day growth period were determined in both cases. The length of the cell cycle and the doubling time calculated from the exponential part of the growth curve were quite similar: Tc = 19 hr and Td = 20 hr for the primary culture, Tc = 17 X 3 hr and Td = 20 hr for the first passage. However, the growth curve and the DNA distribution during the 7-day period showed some differences. The duration of the lag period studied by the growth curve was longer in the primary culture than at the first passage. This phenomenon was also observed using the FCM analysis. The growth fraction determination on the second day of culture was in accordance with the lower proliferation capacity of the cells in primary culture. These data suggest that it would be better to study growth kinetics and drug modifications in articular chondrocytes at the first passage than in primary culture.

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