MiR-181a-5p Delivered by Adipose-Derived Mesenchymal Stem Cell Exosomes Alleviates Klebsiella pneumonia Infection-Induced Lung Injury by Targeting STAT3 Signaling

被引:6
|
作者
Hu, Ren-Jing [1 ]
Chen, Xiao-Chun [2 ]
Xu, Lei [3 ]
Rui, Xiao-Hong [4 ]
Wan, Lin [1 ]
Lu, Jie [1 ]
Liu, Jun [4 ]
Pei, Hao [4 ]
机构
[1] Nanjing Med Univ, Dept Lab Med, Wuxi Peoples Hosp 2, Wuxi 214000, Jiangsu, Peoples R China
[2] Taizhou Second Peoples Hosp, Dept Lab Med, Taizhou 225411, Jiangsu, Peoples R China
[3] Wuxi Stomatol Hosp, Dept Oral & Maxillofacial Surg, Wuxi 214001, Jiangsu, Peoples R China
[4] Wuxi Fifth Peoples Hosp, Dept Lab Med, Wuxi 214000, Jiangsu, Peoples R China
关键词
METASTASIS;
D O I
10.1155/2022/5188895
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background. Klebsiella pneumoniae (K. pneu) is a leading cause of gram-negative pneumonia, which requires effective treatment. Adipose-derived mesenchymal stem cell- (ADSC-) derived exosomal microRNAs (miRNAs) have presented the inhibitory effect of multiple diseases. However, the function of ADSC-derived exosomal miRNAs in K. pneu remains unclear. Aim. In this study, we aimed to explore the effect of ADSC-derived exosomal miR-181-5p on K. pneu infection-induced lung injury. Methods. C57BL/6 mouse model was established by infection of K. pneu. ADSCs and exosomes were extracted and characterized in vitro. The translocation of ADSC-derived exosomes to bone marrow-derived macrophages (BMDMs) was detected. The level of miR-181a-5p was detected by real-time PCR. The secretion of inflammatory factors was determined by ELISA. The interaction between miR-181a-5p with STAT3 was identified. Results. We successfully isolated the ADSCs that express positive markers CD90 and CD105 rather than CD31 and CD45. The exosomal miR-181a-5p secreted by ADSCs were internalized by BMDM and K. pneu infection stimulated the miR-181a-5p level in bronchoalveolar lavage fluid (BALF) and BMDM. ADSC-derived exosomal miR-181a-5p repressed pulmonary outgrowth and dissemination of K. pneu infection in mice, repressed cellular infiltration in lung tissue, and attenuated the inflammasome activity and the levels of IL-1 beta and IL-18 in the lung. Mechanically, miR-181a-5p was able to inhibit STAT3 expression at posttranscriptional levels and repressed Nlrp3 and Asc expression in BMDM. Conclusion. Consequently, we concluded that ADSC-derived exosomal miR-181a-5p alleviated Klebsiella pneumonia infection-induced lung injury by targeting STAT3 signaling. ADSC-derived exosomal miR-181a-5p may serve as a potential candidate for the treatment of Klebsiella pneumonia infection-induced lung injury.
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页数:11
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