4.7 Article

Lipopolysaccharide-Preconditioned Dental Follicle Stem Cells Derived Small Extracellular Vesicles Treating Periodontitis via Reactive Oxygen Species/ Mitogen-Activated Protein Kinase Signaling-Mediated Antioxidant Effect

Journal

INTERNATIONAL JOURNAL OF NANOMEDICINE
Volume 17, Issue -, Pages 799-819

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJN.S350869

Keywords

small extracellular vesicle; dental follicle stem cell; periodontitis; reactive oxygen species; antioxidant effect

Funding

  1. National Key Research and Development Program of China [2017YFA0104800]
  2. Key Research and Development Program of Sichuan Province [2020YFS0175]

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LPS-preconditioned DFC-sEV can effectively be used as an auxiliary method for periodontitis treatment through antioxidant effects in the subgingival environment. It reduces the RANKL/OPG ratio of PDLSCs under inflammatory conditions by inhibiting the ROS/JNK signaling and promotes macrophages to polarize toward the M2 phenotype via ROS/ERK signaling. Loading LPS-preconditioned DFC-sEV with the HA injectable system allows sustained release of sEV and enhances therapeutic efficacy for periodontitis in canines.
Purpose: Lipopolysaccharide (LPS) pretreatment can enhance the therapeutic effect of dental follicle stem cells-derived small extracellular vesicles (DFC-sEV) for periodontitis, and this study aimed to investigate the underlying mechanisms and clinical application Of LPS-preconditioned DFC-sEV in periodontitis. Methods: The protein spectrum of DFC-sEV before and after LPS pretreatment was determined by liquid chromatography-tandem mass spectrometry and bioinformatic analysis. Their effects on inflammatory periodontal ligament stem cells (PDLSCs) and macrophages were investigated for cell proliferation, migration, type 2 macrophage (M2) polarization, and intracellular reactive oxygen species (ROS) levels separately. In addition, the regulation of ROS/Jun amino-terminal kinases (JNK) and ROS/extracellular signalrelated kinases (ERK) signaling by LPS-preconditioned DFC-sEV was also studied to reveal the antioxidant mechanism. In vivo, two kinds of DFC-sEV loaded with 0.2% hyaluronic acid (HA) gel were applied for canine periodontitis to evaluate the therapeutic potential. Results: The proteomic analysis showed that thirty-eight proteins were differentially expressed in LPS-preconditioned DFC-sEV, and interestingly, the highly expressed proteins were mainly involved in antioxidant and enzyme-regulating activities. In addition to promoting PDLSCs and macrophage proliferation, LPS-preconditioned DFC-sEV inhibited intracellular ROS as an antioxidant. It reduced the RANKL/OPG ratio of PDLSCs by inhibiting ROS/JNK signaling under inflammatory conditions and promoted macrophages to polarize toward the M2 phenotype via ROS/ERK signaling. Furthermore, LPS-preconditioned DFC-sEV loaded with the HA injectable system could sustainably release sEV and enhance the therapeutic efficacy for periodontitis in canines. Conclusion: LPS-preconditioned DFC-sEV could be effectively used as an auxiliary method for periodontitis treatment via antioxidant effects in a subgingival environment, and loading it with HA is feasible and effective for clinical applications.

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