Aucubin inhibits IL-1β- or TNF-α-induced extracellular matrix degradation in nucleus pulposus cell through blocking the miR-140-5p/CREB1 axis

J Cell Physiol. 2019 Aug;234(8):13639-13648. doi: 10.1002/jcp.28044. Epub 2019 Jan 13.

Abstract

In intervertebral disc degeneration (IDD), increased proinflammatory molecules secreted by human nucleus pulposus cells (HNPCs) could promote the expression of extracellular matrix (ECM)-degrading enzymes. IDD could be affected by both genetic and environmental factors, including microRNAs (miRNAs). Aucubin, the active ingredient of a traditional Chinese medicine herb Du Zhong, has been reported to promote osteogenic differentiation; however, the role of aucubin in IDD and the underlying mechanism remain unclear. Herein, we evaluated the effect of aucubin on TNF-α- or IL-1β-induced ECM degradation in HNPCs. By using online tools, miR-140 was selected as a candidate miRNA that is related to TNF-α or IL-1β signaling. Overexpression of miR-140 enhanced the effect of aucubin on ECM degradation. Moreover, cAMP responsive element binding protein 1 (CREB1), a major transcriptional factor in immune-related signaling, was a direct downstream target of miR-140. CREB1 knockdown mimicked the function of miR-140 overexpression on ECM degradation. In summary, aucubin might ameliorate IL-1β- or TNF-α-induced ECM degradation in HNPCs through regulating miR-140/CREB1.

Keywords: IL-1β; TNF-α; aucubin; cAMP responsive element binding protein 1; intervertebral disc degeneration; miR-140.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Cells, Cultured
  • Cyclic AMP Response Element-Binding Protein / drug effects*
  • Cyclic AMP Response Element-Binding Protein / metabolism
  • Extracellular Matrix / metabolism
  • Extracellular Matrix / pathology
  • Female
  • Humans
  • Interleukin-1beta / drug effects*
  • Interleukin-1beta / metabolism
  • Intervertebral Disc Degeneration / metabolism
  • Intervertebral Disc Degeneration / pathology
  • Iridoid Glucosides / pharmacology*
  • Male
  • MicroRNAs / drug effects*
  • MicroRNAs / metabolism
  • Middle Aged
  • Nucleus Pulposus / drug effects*
  • Signal Transduction / drug effects
  • Tumor Necrosis Factor-alpha / drug effects*
  • Tumor Necrosis Factor-alpha / metabolism
  • Young Adult

Substances

  • CREB1 protein, human
  • Cyclic AMP Response Element-Binding Protein
  • IL1B protein, human
  • Interleukin-1beta
  • Iridoid Glucosides
  • MicroRNAs
  • Mirn140 microRNA, human
  • Tumor Necrosis Factor-alpha
  • aucubin