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人单核细胞释放的可溶性细胞生长抑制因子。II. 对靶细胞动力学的影响。

Soluble cytostatic factor(s) released from human monocytes. II. Effects on target cell kinetics.

作者信息

Eggen B M, Bakke O, Hammerstrøm J

出版信息

Scand J Immunol. 1983 Jul;18(1):13-20. doi: 10.1111/j.1365-3083.1983.tb00830.x.

Abstract

Human monocytes release a stable cytostatic factor during in vitro culture after stimulation with lymphokine and endotoxin. The cell cycle time of synchronized NHIK 3025 cells increased from 20.3 to 23.2 h in the first cell cycle when the target cells were exposed to the factor during the whole cell cycle. In exponentially growing NHIK 3025 cell cultures the cell doubling time increased from 18.9 h to 23.1 h under continuous factor exposure for 70 h. These cells regained normal cell division rate when fresh culture medium replaced the cytostatic factor. Continuous exposure to the cytostatic factor for 96 h increased the cell doubling time of asynchronous K-562 cells from 19.7 to 31.8 h. The target cell DNA synthesis, evaluated by thymidine incorporation, was markedly depressed after culture with the factor for 24 h, and this depression was detectable already within 4 h of culture. The factor showed no cytolytic effect on the two cell lines tested. The cytostatic factor influenced the cell cycle distribution of both target cells tested, since cell cycle analysis by DNA flow cytometry demonstrated a reversible inhibition of factor-exposed NHIK 3025 cells in G1- and early S-phase, whereas K-562 cells accumulated in G1-phase.

摘要

人单核细胞在受到淋巴因子和内毒素刺激后,于体外培养过程中释放出一种稳定的细胞生长抑制因子。当靶细胞在整个细胞周期中暴露于该因子时,同步化的NHIK 3025细胞在第一个细胞周期中的细胞周期时间从20.3小时增加到23.2小时。在指数生长的NHIK 3025细胞培养物中,在持续暴露于该因子70小时的情况下,细胞倍增时间从18.9小时增加到23.1小时。当新鲜培养基替换细胞生长抑制因子后,这些细胞恢复了正常的细胞分裂速率。将异步K - 562细胞持续暴露于细胞生长抑制因子96小时,其细胞倍增时间从19.7小时增加到31.8小时。通过胸苷掺入评估的靶细胞DNA合成,在用该因子培养24小时后显著降低,并且在培养4小时内即可检测到这种降低。该因子对所测试的两种细胞系均无细胞溶解作用。细胞生长抑制因子影响了所测试的两种靶细胞的细胞周期分布,因为通过DNA流式细胞术进行的细胞周期分析表明,暴露于该因子的NHIK 3025细胞在G1期和早期S期受到可逆性抑制,而K - 562细胞则在G1期积累。

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