Baruque G A, Bitencourt M A, Pasquini R, Castelo-Branco M T L, Llerena J C, Rumjanek V M
Instituto de Bioquímica Médica/CCS - UFRJ, and Instituto de Biofísica Carlos Chagas Filho/CCS - UFRJ, Rio de Janeiro, Brazil.
Cell Prolif. 2007 Aug;40(4):558-67. doi: 10.1111/j.1365-2184.2007.00446.x.
Deregulated apoptosis might be involved in some of the features of Fanconi anaemia (FA). The possibility that the pro-apoptotic Bax protein could be involved in an increased susceptibility to apoptosis in FA patients was investigated.
Intracellular Bax expression, Bcl-2 expression (an anti-apoptotic protein) and cell death were analysed in 26 FA peripheral blood lymphocyte samples.
Most FA samples (69%) displayed increased levels of Bax and were more susceptible to both spontaneous apoptosis and mitogen activation-induced cell death. Two subgroups were identified: one presented elevated levels of Bax (n = 18), whereas the other (n = 8), had Bax levels lower than controls. Two subgroups based on Bcl-2 expression were also identified: one with normal and another with high Bcl-2 expression. No inverse correlation was found between Bcl-2 levels and Bax expression. A clear difference in susceptibility to induced cell death could be observed between control and FA samples. The best correlation was observed between high levels of Bax and mitogen-induced apoptosis of cells; these displayed characteristics of necrosis secondary to apoptosis, suggesting that the intrinsic apoptotic pathway was being activated.
Despite increased susceptibility to cell death induction, there was no correlation between Bax levels, chromosome breakage, haematological parameters or androgen therapy. The importance of apoptosis and Bax expression in the clinical development of FA awaits clarification.
凋亡失调可能与范可尼贫血(FA)的某些特征有关。研究了促凋亡蛋白Bax可能参与FA患者对凋亡易感性增加的可能性。
分析了26例FA外周血淋巴细胞样本中的细胞内Bax表达、Bcl-2表达(一种抗凋亡蛋白)和细胞死亡情况。
大多数FA样本(69%)显示Bax水平升高,并且对自发凋亡和丝裂原激活诱导的细胞死亡更敏感。确定了两个亚组:一个亚组Bax水平升高(n = 18),而另一个亚组(n = 8)的Bax水平低于对照组。还根据Bcl-2表达确定了两个亚组:一个亚组Bcl-2表达正常,另一个亚组Bcl-2表达高。未发现Bcl-2水平与Bax表达之间存在负相关。在对照样本和FA样本之间可观察到对诱导细胞死亡的易感性存在明显差异。在高水平Bax与丝裂原诱导的细胞凋亡之间观察到最佳相关性;这些细胞表现出继发于凋亡的坏死特征,表明内在凋亡途径被激活。
尽管对细胞死亡诱导的易感性增加,但Bax水平、染色体断裂、血液学参数或雄激素治疗之间无相关性。凋亡和Bax表达在FA临床发展中的重要性有待阐明。