TIGAR mediates the inhibitory role of hypoxia on ROS production and apoptosis in rat nucleus pulposus cells

• Published in: Osteoarthritis and cartilage Vol. 26; no. 1; pp. 138 - 148
• Main Authors: Jiang, L.-B., Cao, L., Ma, Y.-Q., Chen, Q., Liang, Y., Yuan, F.-L., Li, X.-L., Dong, J., Chen, N.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.01.2018
• Subjects: Adult; Animals; Apoptosis - physiology; Apoptosis Regulatory Proteins; Disease Models, Animal; Female; Humans; Hypoxia; Hypoxia - physiopathology; Intervertebral Disc Degeneration; Intracellular Signaling Peptides and Proteins - metabolism; Intracellular Signaling Peptides and Proteins - physiology; Male; Nucleus pulposus; Nucleus Pulposus - metabolism; Proteins; Rats, Sprague-Dawley; Reactive oxygen species; Reactive Oxygen Species - metabolism; RNA, Small Interfering - administration & dosage; TP53-induced glycolysis and apoptosis regulator; Transfection; Up-Regulation; Young Adult; Intervertebral disc degeneration; Hypoxia; Reactive oxygen species; Nucleus pulposus; TP53-induced glycolysis and apoptosis regulator
• ISSN: 1063-4584; 1522-9653
• DOI: 10.1016/j.joca.2017.10.007

Hypoxia has been shown to inhibit reactive oxygen species (ROS) production in nucleus pulposus (NP) cells. The TP53-induced glycolysis and apoptosis regulator (TIGAR) has been reported to suppress oxidative stress. We sought to explore the role of TIGAR in the effect of hypoxia on ROS production and apoptosis. An intervertebral disc degeneration (IDD) model of Sprague–Dawley (SD) rat caudal spine was established by puncturing the Co6–7 disc. TIGAR expression was detected by immunohistochemistry and western blotting in human and SD rat NP tissues of degenerated discs. Rat primary NP cells treated with hypoxia and cobalt chloride (CoCl2) were analyzed by western blotting for TIGAR expression. After TIGAR silence with TIGAR siRNA transfection, apoptosis percentage, mitochondrial and total intracellular ROS levels were measured. H2O2 was used to further check the effects of TIGAR on oxidative stress. Finally, NADPH/NADP+ and GSH/GSSH ratio were examined after TIGAR silencing under hypoxic conditions and after H2O2 treatment. A degree-dependent increase in TIGAR expression was observed in human and rat degenerated NP tissues. Hypoxia and hypoxia-inducer CoCl2 enhanced TIGAR and P53 expressions in rat NP cells. TIGAR silence reversed the inhibitory effects of hypoxia on intracellular and mitochondrial ROS production, as well as apoptosis percentage. However, TIGAR silence aggravated H2O2-induced ROS production. In addition, TIGAR increased NADPH/NADP+ and GSH/GSSH ratio in NP cells. These results suggested that TIGAR appears to mediate the protective role of hypoxia on ROS production and apoptosis percentage by enhancing NADPH/NADP+ and GSH/GSSH ratio.