Propionibacterium acnes induces intervertebral disc degeneration by promoting nucleus pulposus cell apoptosis via the TLR2/JNK/mitochondrial-mediated pathway

Emerg Microbes Infect. 2018 Jan 10;7(1):1. doi: 10.1038/s41426-017-0002-0.

Abstract

Evidence suggests that intervertebral disc degeneration (IVDD) can be induced by Propionibacterium acnes (P. acnes), although the underlying mechanisms are unclear. In this study, we analyzed the pathological changes in degenerated human intervertebral discs (IVDs) infected with P. acnes. Compared with P. acnes-negative samples, P. acnes-positive IVDs showed increased apoptosis of nucleus pulposus cells (NPCs) concomitant with severe IVDD. Then, a P. acnes-inoculated IVD animal model was established, and severe IVDD was induced by P. acnes infection by promoting NPC apoptosis. The results suggested that P.acnes-induced apoptosis of NPCs via the Toll-like receptor 2 (TLR2)/c-Jun N-terminal kinase (JNK) pathway and mitochondrial-mediated cell death. In addition, P. acnes was found to activate autophagy, which likely plays a role in apoptosis of NPCs. Overall, these findings further validated the involvement of P. acnes in the pathology of IVDD and provided evidence that P. acnes-induced apoptosis of NPCs via the TLR2/JNK pathway is likely responsible for the pathology of IVDD.

MeSH terms

  • Adult
  • Aged
  • Animals
  • Apoptosis*
  • Autophagy
  • Female
  • Humans
  • Intervertebral Disc / microbiology
  • Intervertebral Disc / pathology
  • Intervertebral Disc / surgery
  • Intervertebral Disc Degeneration / etiology
  • Intervertebral Disc Degeneration / microbiology*
  • Intervertebral Disc Degeneration / physiopathology
  • MAP Kinase Kinase 4 / metabolism*
  • Male
  • Mice
  • Middle Aged
  • Nucleus Pulposus / cytology
  • Nucleus Pulposus / pathology*
  • Propionibacterium acnes / isolation & purification
  • Propionibacterium acnes / physiology*
  • Toll-Like Receptor 2 / metabolism*

Substances

  • TLR2 protein, human
  • Tlr2 protein, mouse
  • Toll-Like Receptor 2
  • MAP Kinase Kinase 4