Reactive oxygen species-dependent HSP90 protein cleavage participates in arsenical As + 3 - and MMA + 3 -induced apoptosis through inhibition of telomerase activity via JNK activation

Abstract

The effects of six arsenic compounds including As + 3 , MMA + 3 , DMA + 3 , As + 5 , MMA + 5 , and DMA + 5 on the viability of NIH3T3 cells were examined. As + 3 and MMA + 3 , but not the others, exhibited significant cytotoxic effects in NIH3T3 cells through apoptosis induction. The apoptotic events such as DNA fragmentation and chromosome condensation induced by As + 3 and MMA + 3 were prevented by the addition of NAC and CAT, and induction of HO-1 gene expression in accordance with cleavage of the HSP90 protein, and suppression of telomerase activity were observed in NIH3T3 cells under As + 3 and MMA + 3 treatments. An increase in the intracellular peroxide level was examined in As + 3 - and MMA + 3 -treated NIH3T3 cells, and As + 3 - and MMA + 3 -induced apoptotic events were blocked by NAC, CAT, and DPI addition. HSP90 inhibitors, GA and RD, significantly attenuated the telomerase activity in NIH3T3 cells with an enhancement of As + 3 - and MMA + 3 -induced cytotoxicity. Suppression of JNKs significantly inhibited As + 3 - and MMA + 3 -induced apoptosis by blocking HSP90 protein cleavage and telomerase reduction in NIH3T3 cells. Furthermore, Hb, SnPP, and dexferosamine showed no effect against As + 3 - and MMA + 3 -induced apoptosis, and overexpression of HO-1 protein or inhibition of HO-1 protein expression did not affect the apoptosis induced by As + 3 or MMA + 3 . These data provide the first evidence to indicate that apoptosis induced by As + 3 and MMA + 3 is mediated by an ROS-dependent degradation of HSP90 protein and reduction of telomerase via JNK activation, and HO-1 induction might not be involved.