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Preconditioning mesenchymal stromal cells with flagellin enhances the anti‑inflammatory ability of their secretome against lipopolysaccharide‑induced acute lung injury

  • Authors:
    • Rui Li
    • Yu Li
    • Xiaoyan Dong
  • View Affiliations / Copyright

    Affiliations: Department of Pulmonary, Shanghai Children's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200062, P.R. China, Department of Plastic and Reconstructive Surgery, Shanghai Key Laboratory of Tissue Engineering, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, P.R. China
    Copyright: © Li et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 2753-2766
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    Published online on: July 28, 2020
       https://doi.org/10.3892/mmr.2020.11380
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Abstract

Acute lung injury (ALI) is a complex condition frequently encountered in the clinical setting. The aim of the present study was to investigate the effect of conditioned media (CM) from human adipose‑derived mesenchymal stromal cells (MSCs) activated by flagellin (F‑CM), a Toll‑like receptor 5 ligand, on inflammation‑induced lung injury. In the in vitro study, RAW264.7 macrophages treated with F‑CM had a higher proportion of cells with the M2 phenotype, lower expression of pro‑inflammatory factors and stronger expression of anti‑inflammatory genes compared with the CM from normal adipose‑derived MSCs. Furthermore, in vivo experiments were performed in mice with ALI induced by intraperitoneal injection of lipopolysaccharide. F‑CM significantly alleviated the lung exudation, inhibited inflammatory cell recruitment in lung tissues and decreased the concentration of inflammatory factors in the bronchoalveolar lavage fluid. These findings indicated that F‑CM has superior anti‑inflammation ability compared with CM, and that it may represent a promising therapeutic approach to the treatment of inflammation‑induced ALI.
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Copy and paste a formatted citation
Spandidos Publications style
Li R, Li Y and Dong X: Preconditioning mesenchymal stromal cells with flagellin enhances the anti‑inflammatory ability of their secretome against lipopolysaccharide‑induced acute lung injury. Mol Med Rep 22: 2753-2766, 2020.
APA
Li, R., Li, Y., & Dong, X. (2020). Preconditioning mesenchymal stromal cells with flagellin enhances the anti‑inflammatory ability of their secretome against lipopolysaccharide‑induced acute lung injury. Molecular Medicine Reports, 22, 2753-2766. https://doi.org/10.3892/mmr.2020.11380
MLA
Li, R., Li, Y., Dong, X."Preconditioning mesenchymal stromal cells with flagellin enhances the anti‑inflammatory ability of their secretome against lipopolysaccharide‑induced acute lung injury". Molecular Medicine Reports 22.4 (2020): 2753-2766.
Chicago
Li, R., Li, Y., Dong, X."Preconditioning mesenchymal stromal cells with flagellin enhances the anti‑inflammatory ability of their secretome against lipopolysaccharide‑induced acute lung injury". Molecular Medicine Reports 22, no. 4 (2020): 2753-2766. https://doi.org/10.3892/mmr.2020.11380
Copy and paste a formatted citation
x
Spandidos Publications style
Li R, Li Y and Dong X: Preconditioning mesenchymal stromal cells with flagellin enhances the anti‑inflammatory ability of their secretome against lipopolysaccharide‑induced acute lung injury. Mol Med Rep 22: 2753-2766, 2020.
APA
Li, R., Li, Y., & Dong, X. (2020). Preconditioning mesenchymal stromal cells with flagellin enhances the anti‑inflammatory ability of their secretome against lipopolysaccharide‑induced acute lung injury. Molecular Medicine Reports, 22, 2753-2766. https://doi.org/10.3892/mmr.2020.11380
MLA
Li, R., Li, Y., Dong, X."Preconditioning mesenchymal stromal cells with flagellin enhances the anti‑inflammatory ability of their secretome against lipopolysaccharide‑induced acute lung injury". Molecular Medicine Reports 22.4 (2020): 2753-2766.
Chicago
Li, R., Li, Y., Dong, X."Preconditioning mesenchymal stromal cells with flagellin enhances the anti‑inflammatory ability of their secretome against lipopolysaccharide‑induced acute lung injury". Molecular Medicine Reports 22, no. 4 (2020): 2753-2766. https://doi.org/10.3892/mmr.2020.11380
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