Sunjic Suzana Borovic, Cipak Ana, Rabuzin Filip, Wildburger Renate, Zarkovic Neven
Division of Molecular Medicine, Rudjer Boskovic Institute, Zagreb, Croatia.
Biofactors. 2005;24(1-4):141-8. doi: 10.1002/biof.5520240117.
The product of lipid peroxidation, 4-hydroxy-2-nonenal (HNE) is known to cause cell death at high concentrations, while at lower concentrations it can influence cell proliferation and differentiation. In our experiments we used human osteosarcoma cells (HOS), to test the influence of HNE on cell proliferation, differentiation and induction of apoptosis. Apoptosis induction was estimated by TiterTACS TUNEL test. The cells were in parallel counted and the DAPI staining method was used to distinguish between apoptotic and necrotic cells as well as to define the proportion of cells in mitosis. To test the influence of HNE on HOS cell differentiation, cells were treated every second day with HNE. After 10 days, the cells were stained for alkaline phosphatase, a marker for osteoblast differentiation. Cell growth inhibition was caused by supraphysiological concentrations of 10 or 100 microM HNE, while apoptosis was induced with supraphysiological as well as by the physiological amount of the aldehyde (1 microM). Necrosis appeared when cells were treated with 10 or 100 microM, but not with 1 microM HNE. The proportion of cells in mitosis gradually declined with increased HNE concentration. Multiple exposures of HOS cells to 10 microM HNE prevented HOS cell differentiation. These results indicated that HNE inhibits proliferation and differentiation of HOS cells in the same concentration dependent manner as it causes apoptosis. We thus assume that HNE might be one of the important signaling molecules regulating the growth of the human osteosarcoma cells.
脂质过氧化产物4-羟基-2-壬烯醛(HNE)在高浓度时可导致细胞死亡,而在低浓度时则可影响细胞增殖和分化。在我们的实验中,我们使用人骨肉瘤细胞(HOS)来测试HNE对细胞增殖、分化和凋亡诱导的影响。通过TiterTACS TUNEL试验评估凋亡诱导情况。对细胞进行平行计数,并使用DAPI染色法区分凋亡细胞和坏死细胞,以及确定有丝分裂细胞的比例。为了测试HNE对HOS细胞分化的影响,每隔一天用HNE处理细胞。10天后,对细胞进行碱性磷酸酶染色,碱性磷酸酶是成骨细胞分化的标志物。超生理浓度的10或100微摩尔HNE可导致细胞生长抑制,而超生理浓度以及生理量的醛(1微摩尔)均可诱导凋亡。当用10或100微摩尔HNE处理细胞时会出现坏死,但用1微摩尔HNE处理时不会。随着HNE浓度的增加,有丝分裂细胞的比例逐渐下降。HOS细胞多次暴露于10微摩尔HNE可阻止HOS细胞分化。这些结果表明,HNE以与诱导凋亡相同的浓度依赖性方式抑制HOS细胞的增殖和分化。因此,我们推测HNE可能是调节人骨肉瘤细胞生长的重要信号分子之一。