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

被引:15
作者
Li, Xiang [1 ]
Lu, Yang [1 ]
Li, Jiarui [1 ]
Zhou, Shengji [1 ]
Wang, Yuxin [1 ]
Li, Liangping [2 ]
Zhao, Fengchao [1 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Dept Orthopaed Surg, 79 Qingchun Rd, Hangzhou 310003, Peoples R China
[2] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Surg, Hangzhou 310003, Peoples R China
关键词
Photoluminescent carbon-dots; Osteolysis; Mouse-calvarial model; Chemerin-ChemR23; signaling; SIRT1; pathway; NF-KAPPA-B; RANKL-MEDIATED OSTEOCLASTOGENESIS; NEXT-GENERATION; SUPPRESSION; AGENTS; ACTIVATION; ZEBRAFISH; NITROGEN; DEBRIS; CELLS;
D O I
10.1186/s12951-022-01498-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
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-alpha, 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.
引用
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页数:18
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