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.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] miR-125b-5p delivered by adipose-derived stem cell exosomes alleviates hypertrophic scarring by suppressing Smad2
    Xu, Chaolei
    Zhang, Hao
    Yang, Chen
    Wang, Ying
    Wang, Kejia
    Wang, Rui
    Zhang, Wei
    Li, Chao
    Tian, Chenyang
    Han, Chao
    Li, Mengyang
    Liu, Xu
    Wang, Yunwei
    Li, Yan
    Zhang, Jian
    Li, Yu
    Luo, Liang
    Shang, Yage
    Zhang, Lixia
    Chen, Yuxi
    Shen, Kuo
    Hu, Dahai
    BURNS & TRAUMA, 2024, 12
  • [2] Adipose-Derived Mesenchymal Stem Cell-Derived Exosomal miR-301a-3p Regulates Airway Smooth Muscle Cells During Asthma by Targeting STAT3
    Feng, Chen-Ye
    Bai, Shi-Yao
    Li, Meng-Lu
    Zhao, Jie-Yu
    Sun, Jia-Min
    Bao, Hui-Jing
    Ren, Yuan
    Su, Xin-Ming
    JOURNAL OF ASTHMA AND ALLERGY, 2022, 15 : 99 - 110
  • [3] Exosomes derived from miR-181-5p-modified adipose-derived mesenchymal stem cells prevent liver fibrosis via autophagy activation
    Qu, Ying
    Zhang, Qidi
    Cai, Xiaobo
    Li, Fei
    Ma, Zhenzeng
    Xu, Mingyi
    Lu, Lungen
    JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2017, 21 (10) : 2491 - 2502
  • [4] Mechanism of Adipose-Derived Mesenchymal Stem Cell-Derived Extracellular Vesicles Carrying miR-21-5p in Hyperoxia-Induced Lung Injury
    Yunfei Wu
    Zhihui Zhang
    Jun Li
    Hai Zhong
    Rui Yuan
    Zihui Deng
    Xu Wu
    Stem Cell Reviews and Reports, 2022, 18 : 1007 - 1024
  • [5] Mechanism of Adipose-Derived Mesenchymal Stem Cell-Derived Extracellular Vesicles Carrying miR-21-5p in Hyperoxia-Induced Lung Injury
    Wu, Yunfei
    Zhang, Zhihui
    Li, Jun
    Zhong, Hai
    Yuan, Rui
    Deng, Zihui
    Wu, Xu
    STEM CELL REVIEWS AND REPORTS, 2022, 18 (03) : 1007 - 1024
  • [6] Mesenchymal stem cell-conditioned medium alleviates high fat-induced hyperglucagonemia via miR-181a-5p and its target PTEN/AKT signaling
    Song, Jia
    He, Qin
    Guo, Xinghong
    Wang, Lingshu
    Wang, Jinbang
    Cui, Chen
    Hu, Huiqing
    Yang, Mengmeng
    Cui, Yixin
    Zang, Nan
    Yan, Fei
    Liu, Fuqiang
    Sun, Yujing
    Liang, Kai
    Qin, Jun
    Zhao, Ruxing
    Wang, Chuan
    Sun, Zheng
    Hou, Xinguo
    Li, Wenjuan
    Chen, Li
    MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2021, 537
  • [7] miR-129-5p Regulates the Immunomodulatory Functions of Adipose-Derived Stem Cells via Targeting Stat1 Signaling
    Zhang, He-Yang
    Wang, Yu-Han
    Wang, Yan
    Qu, Yan-Nv
    Huang, Xiao-Hui
    Yang, Hui-Xin
    Zhao, Chang-Ming
    He, Youdi
    Li, Si-Wei
    Zhou, Jin
    Wang, Changyong
    Jiang, Xiao-Xia
    STEM CELLS INTERNATIONAL, 2019, 2019
  • [8] LncRNA MIAT knockdown alleviates oxygen-glucose deprivation-induced cardiomyocyte injury by regulating JAK2/STAT3 pathway via miR-181a-5p
    Tan, Jian-Kai
    Ma, Xiao-Feng
    Wang, Guang-Neng
    Jiang, Chang-Rong
    Gong, Hui-Qin
    Liu, Huan
    JOURNAL OF CARDIOLOGY, 2021, 78 (06) : 586 - 597
  • [9] Exosomes Derived from Human Adipose Mesenchymal Stem Cells Inhibits Fibrosis and Treats Oral Submucous Fibrosis via the miR-181a-5p/Smad2 Axis
    Zifei Shao
    Jinhao Xu
    Xiaoyang Xu
    Xiang Wang
    Yuxi Zhou
    Yiyang Li
    Kun Li
    Tissue Engineering and Regenerative Medicine, 2024, 21 : 123 - 135
  • [10] Exosomes Derived from Human Adipose Mesenchymal Stem Cells Inhibits Fibrosis and Treats Oral Submucous Fibrosis via the miR-181a-5p/Smad2 Axis
    Shao, Zifei
    Xu, Jinhao
    Xu, Xiaoyang
    Wang, Xiang
    Zhou, Yuxi
    Li, Yiyang
    Li, Kun
    TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2024, 21 (01) : 123 - 135