Legdeur M C, Bontje P M, Ossenkoppele G J, Beelen R H, van de Loosdrecht A A, Broekhoven M G, Langenhuijsen M M, Thijsen S F, Hofstee H, Schuurhuis G J
Department of Hematology, Free University Hospital, Amsterdam, The Netherlands.
Exp Hematol. 1996 Nov;24(13):1530-9.
Monocytes or monocyte-derived supernatants are able to kill leukemic cells via apoptosis, thereby preferentially effecting more mature leukemic cells. In the present study, the relationship between apoptosis and the apoptosis related proteins, bcl-2 and bax, was investigated in a number of human leukemic cell lines. Monocyte-derived supernatant induces extensive apoptosis in U937 myeloid leukemia cells and minor apoptosis in HL60 cells. No apoptosis was seen in four other cell lines (THP1, HL60-D3, KG1, and K562). The expression of bcl-2 and bax protein was determined in both groups of leukemic cell lines by flow cytometry (bcl-2 and bax) and Western blotting (bcl-2) at baseline level and after incubation with monocyte supernatant after different time periods. No clear relation was found between baseline bcl-2 or bax protein expression and the occurrence of apoptosis after incubation with monocyte supernatant. After different incubation time periods, no change was found in bcl-2 protein expression in U937 and K562 cells, whereas in KG1, HL60, and especially in THP1 cells, a significant decrease could be noticed. On the other hand, there was an increase in bcl-2 expression in HL60-D3 cells. Bax protein expression, measured at the same time points, remained essentially unchanged in HL60-D3 cells, decreased significantly in U937, HL60, and THP1 cells and slightly in K562 cells, and increased significantly in KG1 cells. Also, the ratio bax/bcl-2 decreased in HL60D3, but especially in U937 and HL60 cells, increased slightly in THP1 and KG1 cells, and remained essentially unchanged in K562 cells. Rh-tumor necrosis factor-alpha (TNF-alpha), the main mediator of monocyte mediated cytotoxicity, induced apoptosis in U937, HL60, and THP1 cells, thereby showing changes in bcl-2 expression similar to those found for monocyte derived supernatants. We concluded that in human leukemic cell lines, there is no relation between either bcl-2 or bax protein expression or the ratio of both, and apoptosis mediated by monocyte derived supernatant or TNF-alpha.
单核细胞或单核细胞衍生的上清液能够通过凋亡杀死白血病细胞,从而优先作用于更成熟的白血病细胞。在本研究中,在多种人类白血病细胞系中研究了凋亡与凋亡相关蛋白bcl-2和bax之间的关系。单核细胞衍生的上清液在U937髓系白血病细胞中诱导广泛凋亡,在HL60细胞中诱导轻微凋亡。在其他四种细胞系(THP1、HL60-D3、KG1和K562)中未观察到凋亡。通过流式细胞术(bcl-2和bax)和蛋白质免疫印迹法(bcl-2)在基线水平以及与单核细胞上清液在不同时间段孵育后,测定两组白血病细胞系中bcl-2和bax蛋白的表达。在与单核细胞上清液孵育后,未发现基线bcl-2或bax蛋白表达与凋亡发生之间存在明显关系。在不同的孵育时间段后,U937和K562细胞中bcl-2蛋白表达未发现变化,而在KG1、HL60,尤其是THP1细胞中,可观察到显著下降。另一方面,HL60-D3细胞中bcl-2表达增加。在相同时间点测量的bax蛋白表达,在HL60-D3细胞中基本保持不变,在U937、HL60和THP1细胞中显著下降,在K562细胞中略有下降,在KG1细胞中显著增加。此外,bax/bcl-2比值在HL60D3中降低,但特别是在U937和HL60细胞中升高,在THP1和KG1细胞中略有升高,在K562细胞中基本保持不变。Rh-肿瘤坏死因子-α(TNF-α)是单核细胞介导的细胞毒性的主要介质,在U937、HL60和THP1细胞中诱导凋亡,从而显示出与单核细胞衍生上清液中发现的bcl-2表达变化相似。我们得出结论,在人类白血病细胞系中,bcl-2或bax蛋白表达或两者的比值与单核细胞衍生上清液或TNF-α介导的凋亡之间没有关系。