Copyright
©The Author(s) 2024.
World J Stem Cells. Jun 26, 2024; 16(6): 690-707
Published online Jun 26, 2024. doi: 10.4252/wjsc.v16.i6.690
Published online Jun 26, 2024. doi: 10.4252/wjsc.v16.i6.690
Figure 12 Illustrating the underlying mechanism of combined exogenous mitochondria and adipose-derived mesenchymal stem cells-derived exosomes therapy on protecting the lung parenchyma against acute respiratory distress syndrome-sepsis syndrome induced injury mainly through suppressing inflammation and oxidative stress and refreshing the adenosine triphosphate/mitochondria.
ARDS: Acute respiratory distress syndrome; SS: Sepsis syndrome; ADMSC: Adipose-derived mesenchymal stem cell; CLP: Cecal ligation and puncture; IL: Interleukin; TNF: Tumor necrosis factor; TGF: Transforming growth factor; Drp1: Dynamin-related protein 1; Atg5: Autophagy related 5; ZO-1: Zonula occludens-1; HO-1: Heme oxygenase-1; GR: Glutathione reductase; OXPHOS: Oxidative phosphorylation.
- Citation: Lin KC, Fang WF, Yeh JN, Chiang JY, Chiang HJ, Shao PL, Sung PH, Yip HK. Outcomes of combined mitochondria and mesenchymal stem cells-derived exosome therapy in rat acute respiratory distress syndrome and sepsis. World J Stem Cells 2024; 16(6): 690-707
- URL: https://www.wjgnet.com/1948-0210/full/v16/i6/690.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v16.i6.690