1. Academic Validation
  2. LncRNA NEAT1 promotes nucleus pulposus cell matrix degradation through regulating Nrf2/ARE axis

LncRNA NEAT1 promotes nucleus pulposus cell matrix degradation through regulating Nrf2/ARE axis

  • Eur J Med Res. 2021 Jan 21;26(1):11. doi: 10.1186/s40001-021-00481-2.
Cheng Li 1 Xinjian Ma 2 Chenfei Ni 1 Jingyan Xu 3 Yinfei Xie 3 Junwei Kan 1 Xiaoli Wei 4
Affiliations

Affiliations

  • 1 Department of Rehabilitation Medicine, Affiliated Hospital of Jiangnan University, Wuxi, 214041, Jiangsu, China.
  • 2 Department of Traditional Chinese Medicine, Wuxi Guangrui and Tongjiang Community Health Service Center, Wuxi, 214000, Jiangsu, China.
  • 3 Department of Acupuncture, Affiliated Hospital of Jiangnan University (Formerly the Third People's Hospital), No.585 Xingyuan North Road, Liangxi District, Wuxi, 214041, Jiangsu, China.
  • 4 Department of Acupuncture, Affiliated Hospital of Jiangnan University (Formerly the Third People's Hospital), No.585 Xingyuan North Road, Liangxi District, Wuxi, 214041, Jiangsu, China. xi36267@163.com.
Abstract

Background: This study aimed to assess the role and mechanism of lncRNA NEAT1 in intervertebral disc degeneration (IVD).

Methods: LncRNA profile (GSE56081) between IVD and healthy control was downloaded from the Gene Expression Omnibus (GEO) database and analyzes differential lncRNA expression. Expression of lncRNA NEAT1 in IVD tissue and TNF-α/IL-1β-stimulated nucleus pulposus cells were further measured by RT-PCR. The lncRNA NEAT1 overexpression plasmids (pcDNA-NEAT1) were constructed and transfected into nucleus pulposus cells. Catabolic biomarkers (MMP-3 and MMP-13), anabolic biomarkers (Col II and Aggrecan) and Nrf2 expression were further measured. To further investigate the function of Nrf2, nucleus pulposus cells were pretreated with or without 25 μM tert-Butylhydroquinone (TBHQ), a Nrf2 activator, for 18 h and subsequently cotreated with pcDNA-NEAT1.

Results: A total of 1432 lncRNAs were differentially expressed in GSE56081. Bioinformatic analysis found that these lncRNAs mainly enriched in Nrf2/ARE signaling pathway. LncRNA NEAT1 was highly expressed in IVD tissues than that of healthy control. Moreover, TNF-α/IL-1β induced a time- and dose-dependent increase in the mRNA expression of lncRNA NEAT1 in the nucleus pulposus cells. Overexpression of lncRNA NEAT1 abates promotes nucleus pulposus cells proliferation but induces matrix degradation. Meanwhile, nucleus and cytoplasm Nrf2 expression was significantly down-regulated by lncRNA NEAT1 upregulation. Nrf2 activator (TBHQ) could partially reverse the inhibitory effects of overexpression of lncRNA NEAT1 on matrix degradation.

Conclusion: Collectively, our data unveiled the lncRNA NEAT1 promotes matrix degradation by regulating Nrf2/ARE signaling pathway, suggesting a potential therapeutic for IVD in the future.

Keywords

Intervertebral disc degeneration; LncRNA NEAT1; Nrf2/ARE signaling pathway.

Figures
Products