Malekinejad Hassan, Moradi Masumeh, Fink-Gremmels Johanna
Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.
Department of Veterinary, Pharmacology, Pharmacy and Toxicology, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 104, 3508 TD Utrecht, The Netherlands .
Iran J Pharm Res. 2014 Winter;13(1):191-8.
Mycophenolic acid (MPA) is the active metabolite of mycophenolate mofetil. This study designed to investigate the mechanism of cytotoxicity of MPA on the genetically engineered PC12 Tet Off (PTO) neuronal cells with p53 gene. Alamar Blue (AB) reduction showed concentration-dependent cytotoxicity of MPA on PTO cells with IC50 value of 32.32 ± 4.61 μM. The reactive oxygen species (ROS) generation following exposing the cells to MPA showed a significant (p < 0.05) increase in the ROS production and in a concentration-dependent fashion. Involvement of Caspase 3/7 proteases and Cytochrome C release in the induction of DNA fragmentation are all hallmarks of MPA-induced apoptosis in PTO cells. Our data suggest that MPA exerts an apoptotic effect on PTO cells. Moreover, the apoptotic effect of MPA attribute to the elevation of ROS generation by which might trigger the cytochrome C release and the activation of Caspase 3/7 that ultimately results in DNA fragmentation.
霉酚酸(MPA)是霉酚酸酯的活性代谢产物。本研究旨在探讨MPA对具有p53基因的基因工程化PC12 Tet Off(PTO)神经元细胞的细胞毒性机制。Alamar Blue(AB)还原实验表明MPA对PTO细胞具有浓度依赖性细胞毒性,IC50值为32.32±4.61μM。细胞暴露于MPA后活性氧(ROS)的生成呈浓度依赖性显著增加(p<0.05)。半胱天冬酶3/7蛋白酶的参与以及细胞色素C的释放导致DNA片段化,这些都是MPA诱导PTO细胞凋亡的标志。我们的数据表明MPA对PTO细胞具有凋亡作用。此外,MPA的凋亡作用归因于ROS生成的增加,这可能触发细胞色素C的释放以及半胱天冬酶3/7的激活,最终导致DNA片段化。