Chitosan hydrogel incorporated with dental pulp stem cell-derived exosomes alleviates periodontitis in mice via a macrophage-dependent mechanism

被引:313
作者
Shen, Zongshan [1 ]
Kuang, Shuhong [1 ]
Zhang, Yong [1 ]
Yang, Mingmei [1 ]
Qin, Wei [1 ]
Shi, Xuetao [2 ]
Lin, Zhengmei [1 ]
机构
[1] Sun Yat Sen Univ, Hosp Stomatol, Guanghua Sch Stomatol, Guangdong Prov Key Lab Stomatol, Guangzhou, Guangdong, Peoples R China
[2] South China Univ Technol, Natl Engn Res Ctr Tissue Restorat & Reconstruct, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
Dental pulp stem cells; Exosomes; Chitosan hydrogel; Periodontitis; Macrophages; INFLAMMATION; POLARIZATION; DISEASES;
D O I
10.1016/j.bioactmat.2020.07.002
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Periodontitis is caused by host immune-inflammatory response to bacterial insult. A high proportion of proinflammatory 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.
引用
收藏
页码:1113 / 1126
页数:14
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