摘要
AIM: To investigate the roles of PLCγ2 and PKCα in TPA-induced apoptosis of gastric cancer cells.METHODS: Human gastric cancer cell line MGC80-3 was used. Protein expression levels of PLCγ2 and PKCα were detected by Western blot. Protein localization of PLCγ2 and PKCα was shown by immunofluoscence analysis under laserscanning confocal microscope. Apoptotic morphology was observed by DAPI fluorescence staining, and apoptotic index was counted among 1 000 cells randomly.RESULTS: Treatment of gastric cancer cells MGC80-3 with TPA not only up-regulated expression of PLC-γ2 protein,but also induced PLC-γ2 translocation from the cytoplasm to the nucleus. However, this process was not directly associated with apoptosis induction. Further investigation showed that PKCa translocation from the cytoplasm to the nucleus was correlated with initiation of apoptosis. To explore the inevitable linkage between PLC-γ2 and PKCα during apoptosis induction,PLC inhibitor U73122 was used to block PLC-γ2 translocation,in which neither stimulating PKCα translocation nor inducing apoptosis occurred in MGC80-3 cells. However, when U73122treated cells were exposed to TPA, not only PLC-γ2, but also PKCα was redistributed. On the other hand, when cells were treated with PKC inhibitor alone, PLC-γ2 protein was still located in the cytoplasm. However, redistribution of PLC-γ2 protein occurred in the presence of TPA, no matter whether PKC inhibitor existed or not.CONCLUSION: PLC-γ2 translocation is critical in transmitting TPA signal to its downstream molecule PKCα. As an effector,PKCα directly promotes apoptosis of MGC80-3 cells.Therefore, protein translocation of PLCγ2 and PKCα is critical event in the process of apoptosis induction.
AIM:To investigate the roles of PLCγ2 and PKCα in TPA- induced apoptosis of gastric cancer cells. METHODS:Human gastric cancer cell line MGC80-3 was used.Protein expression levels of PLCγ2 and PKCα were detected by Western blot.Protein localization of PLCγ2 and PKCα was shown by immunofluoscence analysis under laser- scanning confocal microscope.Apoptotic morphology was observed by DAPI fluorescence staining,and apoptotic index was counted among 1 000 cells randomly. RESULTS:Treatment of gastric cancer cells MGC80-3 with TPA not only up-regulated expression of PLC-γ2 protein, but also induced PLC-γ2 translocation from the cytoplasm to the nucleus.However,this process was not directly associated with apoptosis induction.Further investigation showed that PKCa translocation from the cytoplasm to the nucleus was correlated with initiation of apoptosis.To explore the inevitable linkage between PLC-γ2 and PKCα during apoptosis induction, PLC inhibitor U73122 was used to block PLC-γ2 translocation, in which neither stimulating PKCα translocation nor inducing apoptosis occurred in MGC80-3 cells.However,when U73122- treated cells were exposed to TPA,not only PLC-γ2,but also PKCα was redistributed.On the other hand,when cells were treated with PKC inhibitor alone,PLC-γ2 protein was still located in the cytoplasm.However,redistribution of PLC-γ2 protein occurred in the presence of TPA,no matter whether PKC inhibitor existed or not. CONCLUSION:PLC-γ2 translocation is critical in transmitting TPA signal to its downstream molecule PKCα.As an effector, PKCα directly promotes apoptosis of MGC80-3 cells. Therefore,protein translocation of PLCγ2 and PKCα is critical event in the process of apoptosis induction.
作者
Bing Zhang Qiao Wu Xiao-Feng Ye Su Liu Xiao-Feng Lin Mu-Chuan Chen, Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, School of Life Sciences, Xiamen University, Xiamen 361005, Fujian Province, China Bing Zhang, Medical school, Xiamen University, Xiamen 361005, Fujian Province. China
基金
the National Natural Science Foundation of China(No.30170477)
the National Outstanding Youth Science Foundation of China(No.39825502)
the Natural Science Foundation of Fujian Province(C0110004)
