Feng Yongdong, Hu Junbo, Xie Daxin, Qin Jichao, Zhong Yisheng, Li Xiaolan, Xiao Wei, Wu Jianhong, Tao Deding, Zhang Manchao, Zhu Yunfeng, Song Yuping, Reed Eddie, Li Qingdi Q, Gong Jianping
Tongji Cancer Institute, Department of Surgery, Tongji Hospital, Tongji Medical College, Central China University of Science and Technology, Wuhan, Hubei 430030, P.R. China.
Int J Oncol. 2005 Sep;27(3):699-704.
Caspase-3 is a critical effector caspase for apoptosis, which cleaves proteins, including cytoskeletal and associated proteins, kinases, and members of the Bcl-2 family of apoptosis-related proteins. This leads to changes in apoptotic morphology, such as membrane externalization and cytoplasm and nuclear condensation. It has been reported that pro-caspase-3 is activated in the cytosol. However, it remains obscure how caspase-3 activation correlates to serial changes in cell morphology during apoptosis. The current study was therefore undertaken to assess the relationship between caspase-3 activation and its subcellular localization and alterations in apoptotic morphology in MOLT-4 human leukemia cells exposed to X-ray irradiation. Fluorescence labeled inhibitor of caspases (FLICA) was used to detect caspase-3 activity in apoptotic cells in this project; cell morphology and caspase-3 sub-localization were determined by confocal microscopy. Our data showed that MOLT-4 cells presented typical morphological changes in apoptosis, such as membrane reversion, DNA fragmentation, and formation of apoptotic cell bodies following 10 Gray (Gy) of X-ray irradiation. Caspase-3 was activated 2 h after X-ray irradiation, and its activity increased markedly after 4-6-h exposure. Membrane reversion in MOLT-4 leukemia cells was detected by Annexin V assay at 4 h following X-ray irradiation, 2 h after the elevated caspase-3 activity was measured. Cytologically, activation of caspase-3 was first observed close to the inside surface of the cellular membrane, then transferred to the cytoplasm, and finally translocated to the nuclear region. We conclude that caspase-3 is activated in MOLT-4 cells following exposure to X-rays, and that the enhanced caspase-3 activity and its sub-localization shifting is correlated to changes in apoptotic morphology. The spatial shift of activated caspase-3 in X-ray-induced apoptotic MOLT-4 leukemia cells is a process of crucial importance for apoptosis.
半胱天冬酶 - 3是细胞凋亡过程中的关键效应半胱天冬酶,它能切割蛋白质,包括细胞骨架及相关蛋白、激酶以及凋亡相关蛋白的Bcl - 2家族成员。这会导致凋亡形态的改变,如膜外化以及细胞质和细胞核浓缩。据报道,前半胱天冬酶 - 3在细胞质中被激活。然而,半胱天冬酶 - 3的激活与细胞凋亡过程中细胞形态的一系列变化之间的关联仍不清楚。因此,本研究旨在评估经X射线照射的MOLT - 4人白血病细胞中半胱天冬酶 - 3的激活与其亚细胞定位以及凋亡形态改变之间的关系。在本项目中,使用荧光标记的半胱天冬酶抑制剂(FLICA)检测凋亡细胞中的半胱天冬酶 - 3活性;通过共聚焦显微镜确定细胞形态和半胱天冬酶 - 3的亚定位。我们的数据显示,经10戈瑞(Gy)X射线照射后,MOLT - 4细胞呈现出典型的凋亡形态变化,如膜反转、DNA片段化以及凋亡小体的形成。X射线照射后2小时半胱天冬酶 - 3被激活,照射4 - 6小时后其活性显著增加。在测量到半胱天冬酶 - 3活性升高2小时后,即X射线照射后4小时,通过膜联蛋白V检测法检测到MOLT - 4白血病细胞中的膜反转。从细胞学角度来看,首先在细胞膜内表面附近观察到半胱天冬酶 - 3的激活,然后转移到细胞质中,最后转移至核区域。我们得出结论,MOLT - 4细胞在受到X射线照射后半胱天冬酶 - 3被激活,并且半胱天冬酶 - 3活性的增强及其亚定位的转移与凋亡形态的变化相关。在X射线诱导凋亡的MOLT - 4白血病细胞中,激活的半胱天冬酶 - 3的空间转移是细胞凋亡过程中至关重要的一个过程。