Sodium butyrate protects against oxidative stress in human nucleus pulposus cells via elevating PPARγ-regulated Klotho expression.

Autor: Liu X; Department of Rehabilitation Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, China., Jiang C; Department of Orthopedics, Zhongshan Hospital, Fudan University, Shanghai 200032, China., Liu G; Department of Rehabilitation Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, China., Wang P; Department of Rehabilitation Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, China., Shi M; Department of Rehabilitation Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, China., Yang M; Department of Rehabilitation Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, China., Zhong Z; Department of Rehabilitation Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, China., Ding S; Department of Orthopedics, Zhongshan Hospital, Fudan University, Shanghai 200032, China., Li Y; Department of Rehabilitation Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, China., Liu B; Department of Rehabilitation Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, China. Electronic address: liu.bangzhong@zs-hospital.sh.cn., Cao Y; Department of Orthopedics, Zhongshan Hospital, Fudan University, Shanghai 200032, China. Electronic address: cao.yuanwu@zs-hospital.sh.cn.
Jazyk: angličtina
Zdroj: International immunopharmacology [Int Immunopharmacol] 2020 Aug; Vol. 85, pp. 106657. Date of Electronic Publication: 2020 Jun 15.
DOI: 10.1016/j.intimp.2020.106657
Abstrakt: We investigated the involvement of klotho in the inhibition of oxidative stress by sodium butyrate (NaB) in human nucleus pulposus cells (NPCs). NPCs were pretreated with different concentrations of NaB for 2 h before stimulation with tert-butyl hydroperoxide (TBHP). NaB alleviated TBHP-induced oxidative injury in the NPCs, as evident by the reduced accumulation of mitochondrial superoxide, intracellular reactive oxygen species, and malondialdehyde, and increased activities of superoxide dismutase and glutathione peroxidase. Flow cytometry and western blotting showed that TBHP-induced apoptosis of NPCs was inhibited by NaB. NaB also reduced the TBHP-induced release of proteases that degrade the extracellular matrix, including matrix metalloproteinases 3 and 13, and ADAMTS-4 (a disintegrin and metalloproteinase with thrombospondin motifs 4). Intriguingly, NaB significantly reversed TBHP-induced klotho suppression. However, the protective effects of NaB on NPCs were abolished by klotho-specific small interfering RNA (siRNA). TBHP stimulation had no obvious effects on total or nuclear expression of peroxisome proliferator-activated receptor γ (PPARγ), but significantly reduced PPARγ acetylation and transcriptional activity, which were restored by NaB. TBHP stimulation also promoted the nuclear translocation of histone deacetylase 3 (HDAC3) and enhanced the association between HDAC3 and PPARγ in the nucleus, but this interaction was substantially disrupted by NaB. siRNA-induced HDAC3 knockdown significantly increased PPARγ acetylation and transactivation, reversing the TBHP-induced suppression of klotho. Therefore, NaB alleviates TBHP-induced oxidative stress in human NPCs by elevating PPARγ-regulated klotho expression. HDAC3 may be a critical HDAC subtype that mediates the regulation of PPARγ activity by NaB under oxidative stress.
Competing Interests: Declaration of Competing Interest All authors have no conflicts of interest.
(Copyright © 2020 Elsevier B.V. All rights reserved.)
Databáze: MEDLINE
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