Liu Weidong, Mao Li, Ji Feng, Chen Fengli, Hao Yuedong, Liu Gang
Department of Orthopedics, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.
Department of Endocrinology, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.
Oncotarget. 2017 Feb 7;8(6):10543-10552. doi: 10.18632/oncotarget.14454.
GSK621 is a novel AMP-activated protein kinase (AMPK) activator. This study tested its potential cytoprotective effect in hydrogen peroxide (H2O2)-treated osteoblasts. In cultured MC3T3-E1 osteoblastic cells and primary murine osteoblasts, GSK621 significantly attenuated H2O2-induced cell death and apoptosis. AMPK activation was required for GSK621-induced osteoblast cytoprotection. Inhibition of AMPK, by AMPKα1 T172A mutation or shRNA silence, almost completely blocked GSK621-induced osteoblast cytoprotection. Reversely, introduction of a constitutively-active AMPKα1 (T172D) alleviated H2O2 injuries in MC3T3-E1 cells. Further, GSK621 increased nicotinamide adenine dinucleotide phosphate (NADPH) content in osteoblasts to inhibit H2O2-induced reactive oxygen species (ROS) production. Meanwhile, GSK621 activated cytoprotective autophagy in the osteoblasts. On the other hand, pharmacological inhibition of autophagy alleviated GSK621-mediated osteoblast cytoprotection against H2O2. These results suggest that targeted activation of AMPK by GSK621 ameliorates H2O2-induced osteoblast cell injuries.
GSK621是一种新型的AMP激活蛋白激酶(AMPK)激活剂。本研究测试了其在过氧化氢(H2O2)处理的成骨细胞中的潜在细胞保护作用。在培养的MC3T3-E1成骨细胞和原代小鼠成骨细胞中,GSK621显著减轻了H2O2诱导的细胞死亡和凋亡。GSK621诱导的成骨细胞保护作用需要AMPK激活。通过AMPKα1 T172A突变或shRNA沉默抑制AMPK,几乎完全阻断了GSK621诱导的成骨细胞保护作用。相反,引入组成型激活的AMPKα1(T172D)减轻了MC3T3-E1细胞中的H2O2损伤。此外,GSK621增加了成骨细胞中烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的含量,以抑制H2O2诱导的活性氧(ROS)产生。同时,GSK621激活了成骨细胞中的细胞保护性自噬。另一方面,自噬的药理抑制减轻了GSK621介导的成骨细胞对H2O2的细胞保护作用。这些结果表明,GSK621对AMPK的靶向激活改善了H2O2诱导的成骨细胞损伤。