微泡
牙周炎
牙龈卟啉单胞菌
间质细胞
炎症
骨髓
外体
免疫系统
牙周病原体
细胞生物学
医学
癌症研究
小RNA
生物
免疫学
牙科
基因
生物化学
作者
Congbo Yue,Jun Cao,Andrew Wong,J.H. Kim,Sheikh Alam,Gary Luong,Sushama Talegaonkar,Zvi Schwartz,Barbara D. Boyan,William V. Giannobile,Sinem E. Sahingur,Zhengmei Lin
标识
DOI:10.1177/00220345221084975
摘要
Human bone marrow stromal cell (hBMSC)-derived exosomes are promising therapeutics for inflammatory diseases due to their unique microRNA (miRNA) and protein cargos. Periodontal diseases often present with chronicity and corresponding exuberant inflammation, which leads to loss of tooth support. In this study, we explored whether hBMSC exosomes can affect periodontitis progression. hBMSC exosomes were isolated from cell culture medium through sequential ultracentrifugation. miRNAs and proteins that were enriched in hBMSC exosomes were characterized by RNA sequencing and protein array, respectively. hBMSC exosomes significantly suppressed periodontal keystone pathogen Porphyromonas gingivalis-triggered inflammatory response in macrophages in vitro. Transcriptomic analysis suggested that exosomes exerted their effects through regulating cell metabolism, differentiation, and inflammation resolution. In vivo, weekly exosome injection into the gingival tissues reduced the tissue destruction and immune cell infiltration in rat ligature-induced periodontitis model. Collectively, these findings suggest that hBMSC-derived exosomes can potentially be used as a host modulation agent in the management of periodontitis.
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