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干扰素诱导人造血细胞系和新鲜白血病细胞的细胞周期变化。

Interferon-induced cell cycle changes in human hematopoietic cell lines and fresh leukemic cells.

作者信息

Roos G, Leanderson T, Lundgren E

出版信息

Cancer Res. 1984 Jun;44(6):2358-62.

PMID:6722775
Abstract

A panel of 26 human hematopoietic cell lines was tested for sensitivity to growth inhibition towards interferon-alpha (IFN-alpha) by estimating the effects on cell cycle phase distribution using flow cytometry analysis. The proportion of proliferating cells was assessed by studying the fractional increase of cells in mitosis during a 24-hr vinblastine block. Of 26 cell lines tested, 17 were sensitive to IFN-alpha, and the main cell cycle effect was accumulation in the G0-G1 phase. One Burkitt's lymphoma line, Namalwa, showed a decreased rate of progress through S without any G0/G1 accumulation. Three of the cell lines were also tested with IFN-beta and with IFN-alpha 2 produced by recombinant DNA technology. The latter IFN did not affect one of the cell lines; otherwise, the results were similar to those of IFN-alpha. Six of 16 clinical specimens from patients with hematopoietic neoplasias were IFN-sensitive, all displaying a G0-G1 block. Our results indicate that IFN sensitivity is an individually linked property unrelated to cell origin.

摘要

通过流式细胞术分析评估对细胞周期阶段分布的影响,对一组26种人类造血细胞系进行了针对α干扰素(IFN-α)生长抑制敏感性的测试。通过研究长春碱阻断24小时期间有丝分裂细胞的分数增加来评估增殖细胞的比例。在测试的26种细胞系中,17种对IFN-α敏感,主要的细胞周期效应是在G0-G1期积累。一种伯基特淋巴瘤细胞系Namalwa在S期的进展速率降低,而没有任何G0/G1期积累。其中三种细胞系还用β干扰素和重组DNA技术产生的α2干扰素进行了测试。后一种干扰素对其中一种细胞系没有影响;否则,结果与IFN-α的结果相似。来自造血肿瘤患者的16份临床标本中有6份对IFN敏感,均表现出G0-G1期阻滞。我们的结果表明,IFN敏感性是一种与细胞起源无关的个体相关特性。

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