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. 2023 May 12;14:1125257. doi: 10.3389/fimmu.2023.1125257

Table 3.

The fibrotic target tissues of MSC-EVs.

Target tissues Target cells Results Key mechanisms References
1 Skin Fibroblasts Promotion of proliferation and migration in SSc MiR-29b-3p/PI3K-Akt, Erk1-2, and Smad3-TGF-β1 (110)
Myofibroblasts Suppressing myofibroblasts differentiation MicroRNAs (miR-21, miR-23a, miR-125b, and miR-145)/TGF-β-SMAD2 (111)
2 Lung Lung epithelial cells Better proliferative capacity of alveolar epithelial cell line Activation of FGF2 signaling (112)
Pulmonary vascular endothelial cells Reduction of tissue fibrosis and vascular endothelial remodeling Umbilical cord MSC-exosomal TNF-stimulated gene 6 (113)
Alveolar macrophages Alleviating lung inflammation and fibrosis Polarization of macrophages to m2 anti-inflammatory phenotype (114)
3 Heart Cardiomyocytes Improving cardiac function and alleviating fibrosis MiR-22/methyl CpG binding protein 2 (115)
4 Kidney Tubular epithelial cells Attenuating tubular epithelial-myofibroblast transdifferentiation of renal tubular epithelial cells MiR-335-5p/ADAM19 (116)
5 Colon Intestinal epithelial cells Inhibition of EMT MiR-200b/ZEB1, ZEB2 (117)
Macrophage Reduction of inflammatory cytokines MiR-146a/TRAF6, IRAK1 (118)

MSC-EVs, mesenchymal stem cell-derived extracellular vesicles; MSC, mesenchymal stem cell; EMT, epithelial-to-mesenchymal transition.