Non-Selective Cation Channel-Mediated Ca2+-Entry and Activation of Ca2+/Calmodulin-Dependent Kinase II Contribute to G2/M Cell Cycle Arrest and Survival of Irradiated Leukemia Cells
[摘要] Genotoxic stress induces cell cycle arrest and DNA repair which may enable tumor cells to survive radiation therapy. Here, we defined the role of Ca2+ signaling in the cell cycle control and survival of chronic myeloid leukemia (CML) cells subjected to ionizing radiation (IR). To this end, K562 erythroid leukemia cells were irradiated (0-10 Gy). Tumor survival was analyzed by clonogenic survival assay and cell cycle progression via flow cytometry. Plasma membrane cation conductance was assessed by patch-clamp whole-cell recording and the cytosolic free Ca2+ concentration ([Ca2+]i) was measured by fura-2 Ca2+ imaging. Nuclear activity of Ca2+/calmodulin-dependent kinase II (CaMKII) was defined by Western blotting. In addition, the effect of IR (5 Gy) on the cation conductance of primary CML cells was determined. The results indicated that IR (10 Gy) induced a G2/M cell cycle arrest of K562 cells within 24 h post-irradiation (p.i.) and decreased the clonogenic survival to 0.5 % of that of the control cells. In K562 cells, G2/M cell cycle arrest was preceded by activation of TRPV5/6-like nonselective cation channels in the plasma membrane 1-5 h p.i., resulting in an elevated Ca2+ entry as evident from fura-2 Ca2+ imaging. Similarly, IR stimulated a Ca2+-permeable nonselective cation conductance in primary CML cells within 2-4 h p.i.. Ca2+ entry, into K562 cells was paralleled by an IR-induced activation of nuclear CaMKII. The IR-stimulated accumulation in G2 phase was delayed upon buffering [Ca2+]i with the Ca2+ chelator BAPTA-AM or inhibiting CaMKII with KN93 (1 nM). In addition, KN93 decreased the clonogenic survival of irradiated cells but not of control cells. In conclusion, the data suggest that IR-stimulated cation channel activation, Ca2+ entry and CaMKII activity participate in control of cell cycle progression and survival of irradiated CML cells.
[发布日期] [发布机构]
[效力级别] [学科分类] 分子生物学,细胞生物学和基因
[关键词] Patch-Clamp Recording;Ionizing Radiation;Calcium Signaling;Vanilloid Transient Receptor Potential;Calcium/Calmodulin-Dependent Kinase II;Ratiometric Ca2+ fluorescence imaging [时效性]