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4-羟基壬烯醛对HL-60细胞周期进程及分化相关抗原表达的影响

Effect of 4-Hydroxynonenal on cell cycle progression and expression of differentiation-associated antigens in HL-60 cells.

作者信息

Barrera G, Pizzimenti S, Muraca R, Barbiero G, Bonelli G, Baccino F M, Fazio V M, Dianzani M U

机构信息

Dipartimento di Medicina ed Oncologia Sperimentale, Università di Torino, Italy.

出版信息

Free Radic Biol Med. 1996;20(3):455-62. doi: 10.1016/0891-5849(95)02049-7.

Abstract

4-Hydroxynonenal (HNE) is a highly reactive aldehyde produced by lipid peroxidation of cellular membranes that inhibits growth and induces differentiation in HL-60 cells. Its mechanisms of action were investigated by analyzing the cell cycle distribution and the appearance of differentiated phenotypes in HL-60 cells. Data obtained by exposing cells to DMSO for 7.5 h (same time as for HNE treatment) or for the whole length of the experiments (5 d) were used for comparison. HNE induced a marked increase in the proportion of G0/G1 cells after 1 and 2 d. The brief DMSO treatment did not affect the distribution, whereas continuous exposure led to a progressive accumulation of cells in G0/G1 (maximal at day 5). The proportion of phagocytic cells gradually increased in HNE-treated and DMSO long-exposed cultures from day 2 and peaked at day 5 (35 and 63%, respectively), whereas the effect of the brief DMSO treatment was negligible. The expression of CD11b and CD67 increased in cells treated with HNE or continuously exposed to DMSO, whereas CD36 was expressed at low levels on both treatments. These results indicate that the pathway of the granulocytic differentiation induced by HNE in HL-60 cells differs from that of DMSO: with HNE, growth inhibition precedes the onset of differentiation, whereas in DMSO-treated cells the two processes are chronologically associated.

摘要

4-羟基壬烯醛(HNE)是一种由细胞膜脂质过氧化产生的高反应性醛类物质,它可抑制HL-60细胞的生长并诱导其分化。通过分析HL-60细胞的细胞周期分布和分化表型的出现来研究其作用机制。将细胞暴露于二甲基亚砜(DMSO)7.5小时(与HNE处理时间相同)或整个实验过程(5天)所获得的数据用于比较。HNE处理1天和2天后,G0/G1期细胞的比例显著增加。短暂的DMSO处理不影响细胞分布,而持续暴露则导致细胞在G0/G1期逐渐积累(第5天达到最大值)。从第2天起,在HNE处理组和DMSO长期暴露组中,吞噬细胞的比例逐渐增加,并在第5天达到峰值(分别为35%和63%),而短暂的DMSO处理的影响可忽略不计。用HNE处理或持续暴露于DMSO的细胞中,CD11b和CD67的表达增加,而两种处理方式下CD36的表达水平均较低。这些结果表明,HNE在HL-60细胞中诱导的粒细胞分化途径与DMSO不同:HNE诱导的生长抑制先于分化开始,而在DMSO处理的细胞中,这两个过程在时间上是相关联的。

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