Jin Cheng-Yun, Moon Dong-Oh, Choi Yung Hyun, Lee Jae-Dong, Kim Gi-Young
Department of Microbiology, College of Natural Sciences, Pusan National University, Busan 614-052, Republic of Korea.
Biol Pharm Bull. 2007 Aug;30(8):1432-7. doi: 10.1248/bpb.30.1432.
Agaricus blazei is a medicinal mushroom that possesses antimetastatic, antitumor, antimutagenic, and immunostimulating effects. However, the molecular mechanisms involved in A. blazei-mediated apoptosis remain unclear. In the present study, to elucidate the role of the Bcl-2 in A. blazei-mediated apoptosis, U937 cells were transfected with either empty vector (U937/vec) or vector containing cDNA encoding full-length Bcl-2 (U937/Bcl-2). As compared with U937/vec, U937/Bcl-2 cells exhibited a 4-fold greater expression of Bcl-2. Treatment of U937/vec with 1.0-4.0 mg/ml of A. blazei extract (ABE) for 24 h resulted in a significant induction of morphologic features indicative of apoptosis. In contrast, U937/Bcl-2 exposed to the same ABE treatment only exhibited a slight induction of apoptotic features. ABE-induced apoptosis was accompanied by downregulation of antiapoptotic proteins such as X-linked inhibitor of apoptosis protein (XIAP), inhibitor of apoptosis protein (cIAP)-2 and Bcl-2, activation of caspase-3, and cleavage of poly(ADP-ribose)polymerase (PARP). Ectopic expression of Bcl-2 was associated with significantly induced expression of antiapoptotic proteins, such as cIAP-2 and Bcl-2, but not XIAP. Ectopic expression of Bcl-2 also reduced caspase-3 activation and PARP cleavage in ABE treated U937 cells. Furthermore, treatment with the caspase-3 inhibitor z-DEVD-fmk was sufficient to restore cell viability following ABE treatment. This increase in viability was ascribed to downregulation of caspase-3 and blockage of PARP and PLC-gamma cleavage. ABE also triggered the downregulation of Akt, and combined treatment with LY294002 (an inhibitor of Akt) significantly decreased cell viability. The results indicated that major regulators of ABE-induced apoptosis in human leukemic U937 cells are Bcl-2 and caspase-3, which are associated with dephosphorylation of the Akt signal pathway.
姬松茸是一种具有抗转移、抗肿瘤、抗诱变和免疫刺激作用的药用蘑菇。然而,姬松茸介导的细胞凋亡所涉及的分子机制仍不清楚。在本研究中,为了阐明Bcl-2在姬松茸介导的细胞凋亡中的作用,用空载体(U937/vec)或含有编码全长Bcl-2的cDNA的载体(U937/Bcl-2)转染U937细胞。与U937/vec相比,U937/Bcl-2细胞中Bcl-2的表达高4倍。用1.0-4.0mg/ml的姬松茸提取物(ABE)处理U937/vec 24小时导致明显诱导出指示细胞凋亡的形态学特征。相反,暴露于相同ABE处理的U937/Bcl-2仅表现出轻微的凋亡特征诱导。ABE诱导的细胞凋亡伴随着抗凋亡蛋白如X连锁凋亡抑制蛋白(XIAP)、凋亡抑制蛋白(cIAP)-2和Bcl-2的下调,caspase-3的激活以及聚(ADP-核糖)聚合酶(PARP)的裂解。Bcl-2的异位表达与抗凋亡蛋白如cIAP-2和Bcl-2的显著诱导表达相关,但与XIAP无关。Bcl-2的异位表达还降低了ABE处理的U937细胞中caspase-3的激活和PARP的裂解。此外,用caspase-3抑制剂z-DEVD-fmk处理足以在ABE处理后恢复细胞活力。这种活力的增加归因于caspase-3的下调以及PARP和PLC-γ裂解的阻断。ABE还引发了Akt的下调,并且与LY294002(一种Akt抑制剂)联合处理显著降低了细胞活力。结果表明,人白血病U937细胞中ABE诱导的细胞凋亡的主要调节因子是Bcl-2和caspase-3,它们与Akt信号通路的去磷酸化有关。