Resveratrol protects human nucleus pulposus cells from degeneration by blocking IL-6/JAK/STAT3 pathway

Eur J Med Res. 2021 Jul 28;26(1):81. doi: 10.1186/s40001-021-00555-1.

Abstract

Background: Nucleus pulposus cells' (NPCs') degeneration is mainly responsible for the intervertebral disc degeneration (IDD), which is closely related to inflammatory response. Among the major proinflammatory factors that are related to NPCs' degeneration, interleukin-6 (IL-6) and its downstream JAK/STAT3 pathway have received recent attention. The goal of our study is to figure out whether or how resveratrol (RSV) can protect NPCs from degeneration by affecting IL6/JAK/STAT3 pathway.

Methods: Different concentrations of RSV were added to NPCs' mediums. Cell viability was measured by MTT assay and crystal violet staining. Cell cycle and apoptosis were analyzed by flow cytometry. Protein expression level was determined by western blot. mRNA expression level was measured by qPCR.

Results: Our study showed that RSV improved NPCs' cell viability. It also inhibited cell apoptosis and cell cycle arrest, which were accompanied by the increased expression level of heat shock protein 90 (HSP90) and N-Cadherin. What' more, RSV also improved the NPCs' degeneration which was reflected in the increase of extracellular matrix (collagen II, Aggrecan). Moreover, RSV significantly attenuated the level of IL-6 secretion, which was accompanied by less phosphorylation of the transcription factors Janus kinase 1 (JAK1) and signal transducer and activator of transcription 3 (STAT3).

Conclusion: RSV exerted its protective effect on HNPCs' degeneration by improving cell survival and function. The possible mechanism may be associated with the suppression of JAK/STAT3 phosphorylation and the decreased IL-6 production, which could be explained by a blockage of the positive feedback control loop between IL-6 and JAK/STAT3 pathway.

Keywords: IL-6/JAK/STAT3 pathway; Intervertebral disc degeneration; Nucleus pulposus cells; Positive feedback; Proinflammatory factors; Resveratrol.

MeSH terms

  • Antioxidants / pharmacology
  • Cells, Cultured
  • Gene Expression Regulation / drug effects*
  • Humans
  • Interleukin-6 / antagonists & inhibitors*
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism
  • Intervertebral Disc Degeneration / prevention & control*
  • Janus Kinase 1 / antagonists & inhibitors*
  • Janus Kinase 1 / genetics
  • Janus Kinase 1 / metabolism
  • Nucleus Pulposus / cytology*
  • Nucleus Pulposus / drug effects
  • Nucleus Pulposus / metabolism
  • Resveratrol / pharmacology*
  • STAT3 Transcription Factor / antagonists & inhibitors*
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism

Substances

  • Antioxidants
  • IL6 protein, human
  • Interleukin-6
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • JAK1 protein, human
  • Janus Kinase 1
  • Resveratrol