Primary chondrocyte exosomes mediate osteoarthritis progression by regulating mitochondrion and immune reactivity

Nanomedicine (Lond). 2019 Dec;14(24):3193-3212. doi: 10.2217/nnm-2018-0498.

Abstract

Aim: We aimed to investigate the proteomics of primary chondrocyte exosomes and the effect of exosomes in osteoarthritis (OA) treatment. Materials & methods: We isolated exosomes from primary chondrocytes cultured in normal (D0) and inflammatory environments induced by IL-1β and determined the proteomics of these exosomes. Next, we investigated what effect and mechanism D0 chondrocytes exosomes have in OA treatment. Results: There were more proteins that belonged to mitochondrion and were involved in immune system processes in D0 exosomes. Notably, intra-articular administration of D0 exosomes successfully prevented the development of OA. D0 chondrocyte exosomes could restore mitochondrial dysfunction and polarize macrophage response toward an M2 phenotype. Conclusion: Our findings demonstrated that primary chondrocyte exosomes are efficient in OA treatment.

Keywords: exosomes; immunoregulation; macrophage; mitochondria; osteoarthritis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cells, Cultured
  • Chondrocytes / drug effects
  • Chondrocytes / immunology*
  • Chondrocytes / metabolism*
  • Exosomes / drug effects
  • Exosomes / metabolism*
  • Interleukin-1beta / pharmacology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / metabolism*
  • Osteoarthritis / metabolism*
  • Osteoarthritis / pathology*

Substances

  • Interleukin-1beta