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具有不同细胞周期时间的小鼠表皮亚群的证据。

Evidence of mouse epidermal subpopulations with different cell cycle times.

作者信息

Clausen O P, Kirkhus B, Thorud E, Schjølberg A, Moen E, Cromarty A

出版信息

J Invest Dermatol. 1986 Mar;86(3):266-70. doi: 10.1111/1523-1747.ep12285397.

DOI:10.1111/1523-1747.ep12285397
PMID:3745951
Abstract

In order to obtain information on the distribution of total cell cycle times in hairless mouse epidermis, basal cells were isolated and prepared for DNA flow cytometry at intervals after a pulse labeling with 50 microCi of thymidine. The DNA distributions were recorded, and cells were sorted from windows in the S, G2, and G1 phases of the cell cycle, collected on glass slides, and subjected to autoradiography. The proportions of labeled cells were scored in each fraction, and the percentage of labeled mitoses was determined in histologic sections from the same animals. Grain count distributions were recorded at selected time points over labeled cells in sorted fractions and over labeled mitoses. The movement of the labeled S-phase cohort was thus followed through all cell cycle phases. Peaks in labeled cells were observed at about 36 h in S phase, G2 phase, and mitosis, and high levels of labeled G2 cells and mitoses were seen at about 80 h. These results indicate the existence of one rapidly cycling subpopulation of keratinocytes with a cell cycle time slightly less than 30 h, in addition to keratinocytes with considerably longer cell cycle times. The first peak of labeled G2 cells reached only about 30%. This is consistent with earlier findings of about 30% G2 cells with a rapid traverse, and 70% with a considerably delayed traverse through G2 phase. The proportion of labeled G1 cells reached a value corresponding to twice the initial labeling index at 8 h after pulse labeling. This is consistent with previously obtained phase durations, indicating an unperturbed cell cycle traverse of labeled cells from S phase through G2 and mitosis.

摘要

为了获取无毛小鼠表皮中细胞总周期时间的分布信息,在用50微居里胸苷进行脉冲标记后的不同时间间隔,分离基底细胞并制备用于DNA流式细胞术分析。记录DNA分布情况,从细胞周期的S期、G2期和G1期的窗口中分选细胞,收集到载玻片上,然后进行放射自显影。对每个组分中标记细胞的比例进行评分,并在来自同一动物的组织切片中确定标记有丝分裂的百分比。在选定的时间点记录分选组分中标记细胞以及标记有丝分裂上的颗粒计数分布。由此追踪标记的S期细胞群体在所有细胞周期阶段的移动情况。在S期、G2期和有丝分裂期约36小时观察到标记细胞的峰值,在约80小时观察到高水平的标记G2期细胞和有丝分裂细胞。这些结果表明,除了细胞周期时间长得多的角质形成细胞外,还存在一个快速循环的角质形成细胞亚群,其细胞周期时间略少于30小时。标记G2期细胞的第一个峰值仅达到约30%。这与早期发现的约30%的G2期细胞快速通过,70%的细胞在G2期通过明显延迟的结果一致。脉冲标记后8小时,标记G1期细胞的比例达到对应于初始标记指数两倍的值。这与先前获得的各期持续时间一致,表明标记细胞从S期经过G2期和有丝分裂期的细胞周期进程未受干扰。

相似文献

1
Evidence of mouse epidermal subpopulations with different cell cycle times.具有不同细胞周期时间的小鼠表皮亚群的证据。
J Invest Dermatol. 1986 Mar;86(3):266-70. doi: 10.1111/1523-1747.ep12285397.
2
Cell cycle progression kinetics of regenerating mouse epidermal cells: an in vivo study combining DNA flow cytometry, cell sorting, and [3H]dThd autoradiography.再生小鼠表皮细胞的细胞周期进程动力学:一项结合DNA流式细胞术、细胞分选和[3H]胸苷放射自显影术的体内研究。
J Invest Dermatol. 1986 Apr;86(4):402-5. doi: 10.1111/1523-1747.ep12285672.
3
Effects of pulse labelling with tritiated thymidine on the circadian rhythmicity in epidermal cell-cycle distribution in mice.用氚标记胸腺嘧啶核苷进行脉冲标记对小鼠表皮细胞周期分布昼夜节律的影响。
Cell Tissue Kinet. 1985 Jan;18(1):83-9. doi: 10.1111/j.1365-2184.1985.tb00634.x.
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Subpopulations of slowly cycling cells in S and G2 phase in mouse epidermis.小鼠表皮中处于S期和G2期的慢循环细胞亚群。
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Mathematical model analysis of mouse epidermal cell kinetics measured by bivariate DNA/anti-bromodeoxyuridine flow cytometry and continuous [3H]-thymidine labelling.通过双变量DNA/抗溴脱氧尿苷流式细胞术和连续[3H] - 胸腺嘧啶核苷标记测量的小鼠表皮细胞动力学的数学模型分析
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DNA synthesis in mouse epidermis: S phase cells that remain unlabeled after pulse labeling with DNA precursors progress slowly through S.小鼠表皮中的DNA合成:在用DNA前体进行脉冲标记后仍未标记的S期细胞在S期进展缓慢。
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Ultraviolet B irradiation induces epidermal regeneration with rapidly cycling cells.紫外线B照射可诱导表皮再生,并产生快速增殖的细胞。
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Double labeling autoradiography. Cell kinetic studies with 3H- and 14C-thymidine.双重标记放射自显影术。用³H-和¹⁴C-胸腺嘧啶核苷进行细胞动力学研究。
J Histochem Cytochem. 1981 Jan;29(1A Suppl):109-16.

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Cell Prolif. 2003 Feb;36(1):1-26. doi: 10.1046/j.1365-2184.2003.00257.x.
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Cell Prolif. 1998 Oct-Dec;31(5-6):191-201. doi: 10.1111/j.1365-2184.1998.tb01197.x.