Photoluminescent carbon dots (PCDs) from sour apple: a biocompatible nanomaterial for preventing UHMWPE wear-particle induced osteolysis via modulating Chemerin/ChemR23 and SIRT1 signaling pathway and its bioimaging application

J Nanobiotechnology. 2022 Jun 27;20(1):301. doi: 10.1186/s12951-022-01498-3.

Abstract

Photoluminescent nanomaterials have been widely employed in several biological applications both in vitro and in vivo. For the first time, we report a novel application of sour apple-derived photoluminescent carbon dots (PCDs) for reducing ultra-high molecular weight polyethylene (UHMWPE) wear particle-induced osteolysis using mouse calvarial model. Generally, aseptic prosthetic loosening seems to be a significant postoperative problem for artificial joints replacement, which is mainly contributed by UHMWPE-induced osteolysis. Hence, inhibiting osteoclastic bone-resorption could minimize UHMWPE-induced osteolysis for implant loosening. Prior to osteolysis studies, the prepared sour apple-derived PCDs were employed for bioimaging application. As expected, the prepared PCDs effectively inhibited the UHMWPE particle-induced osteoclastogenesis in vitro. The PCDs treatment effectively inhibited the UHMWPE-induced osteoclast differentiation, F-actin ring pattern, and bone resorption in vitro. Also, the PCDs reduced the UHMWPE-induced ROS stress as well as the expression level of pro-inflammatory cytokines, including TNF-α, IL-1, IL-6, and IL-8. Further, the qPCR and western blot results hypothesized that PCDs inhibited the UHMWPE wear particle-induced osteolysis through suppressing chemerin/ChemR23 signaling and NFATc1 pathway, along with upregulation of SIRT1 expression. Overall, these findings suggest that the synthesized PCDs could be a potential therapeutic material for minimizing UHMWPE particle-induced periprosthetic osteolysis to avoid postoperative complications.

Keywords: Chemerin-ChemR23 signaling; Mouse-calvarial model; Osteolysis; Photoluminescent carbon-dots; SIRT1 pathway.

MeSH terms

  • Animals
  • Biocompatible Materials
  • Carbon / therapeutic use
  • Chemokines / metabolism
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Malus* / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Nanostructures*
  • Osteolysis* / chemically induced
  • Osteolysis* / drug therapy
  • Polyethylenes
  • Signal Transduction
  • Sirtuin 1 / metabolism

Substances

  • Biocompatible Materials
  • Chemokines
  • Intercellular Signaling Peptides and Proteins
  • Polyethylenes
  • chemerin protein, mouse
  • ultra-high molecular weight polyethylene
  • Carbon
  • Sirt1 protein, mouse
  • Sirtuin 1