Distelhorst C W, Lam M, McCormick T S
Department of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Oncogene. 1996 May 16;12(10):2051-5.
The mechanism by which Bcl-2 inhibits apoptosis is unknown. The Bcl-2 protein is localized to intracellular membranes, including the endoplasmic reticulum (ER). The ER is the major intracellular reservoir of Ca2+ in non-muscle cells, sequestering Ca2+ for use in intracellular signaling, and is a prime target of oxidative damage. Because of the recent suggestion that Bcl-2 acts in an antioxidant pathway, we wondered whether Bcl-2 might protect the ER Ca2+ pool in cells exposed to reactive oxygen species. To test this hypothesis, we assessed the effect of hydrogen peroxide (H2O2) treatment on the ER Ca2+ pool in WEH17.2 cells, which do not express Bcl-2, and two stable transfectants, W.Hb13 and W.Hb12. The Bcl-2 level by Western blotting is 4-fold higher in W.Hb12 cells compared to W.Hb13 cells. The ER Ca2+ pool in H2O2-treated and untreated cells was measured according to the amount of Ca2+ mobilized from the ER lumen into the cytoplasm by thapsigargin (TG), a selective inhibitor of the ER (Ca2+)-ATPase. H2O2 treatment produced a significant reduction in the TG-mobilizable Ca2+ pool in WEH17.2 and W.Hb13 cells, but not in W.Hb12 cells, indicating that overexpression of Bcl-2 preserves the integrity of the ER Ca2+ pool in cells exposed to reactive oxygen species.
Bcl-2抑制细胞凋亡的机制尚不清楚。Bcl-2蛋白定位于细胞内膜,包括内质网(ER)。内质网是非肌肉细胞中Ca2+的主要细胞内储存库,它螯合Ca2+用于细胞内信号传导,并且是氧化损伤的主要靶点。由于最近有观点认为Bcl-2在抗氧化途径中起作用,我们想知道Bcl-2是否可能保护暴露于活性氧的细胞中的内质网Ca2+池。为了验证这一假设,我们评估了过氧化氢(H2O2)处理对WEH17.2细胞(不表达Bcl-2)以及两种稳定转染细胞W.Hb13和W.Hb12中内质网Ca2+池的影响。通过蛋白质印迹法检测,W.Hb12细胞中的Bcl-2水平比W.Hb13细胞高4倍。根据内质网(Ca2+)-ATP酶的选择性抑制剂毒胡萝卜素(TG)从内质网腔动员到细胞质中的Ca2+量,测量了H2O2处理和未处理细胞中的内质网Ca2+池。H2O2处理使WEH17.2和W.Hb13细胞中可被TG动员的Ca2+池显著减少,但在W.Hb12细胞中未减少,这表明Bcl-2的过表达可保护暴露于活性氧的细胞中内质网Ca2+池的完整性。