牙周炎
牙髓干细胞
炎症
巨噬细胞
免疫系统
微泡
牙周组织
牙槽
牙髓(牙)
干细胞
癌症研究
化学
免疫学
医学
细胞生物学
牙科
生物
小RNA
体外
生物化学
基因
作者
Zongshan Shen,Shuhong Kuang,Yong Zhang,Mingmei Yang,Wei Qin,Xuetao Shi,Zhengmei Lin
标识
DOI:10.1016/j.bioactmat.2020.07.002
摘要
Periodontitis is caused by host immune-inflammatory response to bacterial insult. A high proportion of pro-inflammatory macrophages to anti-inflammatory macrophages leads to the pathogenesis of periodontitis. As stem cell-derived exosomes can modulate macrophage phenotype, dental pulp stem cell-derived exosomes (DPSC-Exo) can effectively treat periodontitis. In this study, we demonstrated that DPSC-Exo-incorporated chitosan hydrogel (DPSC-Exo/CS) can accelerate the healing of alveolar bone and the periodontal epithelium in mice with periodontitis. Gene Ontology (GO) term enrichment analysis showed that treatment with DPSC-Exo/CS ameliorated periodontal lesion by suppressing periodontal inflammation and modulating the immune response. Specifically, DPSC-Exo/CS facilitated macrophages to convert from a pro-inflammatory phenotype to an anti-inflammatory phenotype in the periodontium of mice with periodontitis, the mechanism of which could be associated with miR-1246 in DPSC-Exo. These results not only shed light on the therapeutic mechanism of DPSC-Exo/CS but also provide the basis for developing an effective therapeutic approach for periodontitis.
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