Table 2.
Selected studies of MSC-derived exosomes in human models.
| Experimental System | MSC | Cargo | Method of exosome isolation | Effect | Study |
|---|---|---|---|---|---|
| PBMC co-culture | Bone marrow (healthy donors) | ND | Ultracentrifugation and precipitation | Suppressed TNF-a & IL-1b but increased anti-inflammatory factor TGF-b in vitro | (80) |
| PBMC co-culture | Bone marrow (healthy donors) | ND | Ultracentrifugation | Increased Treg/Teff ratio and IL-10 concentration in culture medium | (81) |
| Monocyte-derived macrophages | Bone marrow (healthy donors) | ND | Ultracentrifugation | Suppressed pro-inflammatory cytokine production, increased M2 macrophage marker expression, and augmented phagocytic capacity of human monocyte derived macrophages in non-contact cultures | (64) |
| Isolated human pulmonary artery endothelial cells | Umbilical cord | ND | S200 size-exclusion chromatography, differential centrifugation and ultracentrifugation | Regulated STAT3-mediated signaling | (83) |
| Human umbilical cord vein endo- thelial cells (HUVECs) | Bone marrow (healthy donors) | 1,927 proteins identified | Differential centrifugation, filtration and ultracentrifugation | Proteomic analysis of proteins contained in exosomes released by MSC under ischemic like conditions. Mostly proteins such as platelet, epidermal or fibroblast derived growth factors, as well as proteins from nuclear factor-kappaB (NFkB) signaling pathway | (84) |
| HUVEC & human breast carcinoma-derived cell lines | Bone marrow (healthy donors) | miRNA-100 | Differential centrifugation, filtration and ultracentrifugation | Decreased expression of VEGF in breast cancer-derived cells by modulating the mTOR/HIF-1α signaling axis | (85) |
| Comparative study | Bone marrow (healthy donors) | 730 proteins identified in microvesicles | Sucrose cushion centrifugation & ultracentrifugation | Proteomic analysis identified proteins involved in cell proliferation, adhesion, migration, and morphogenesis | (86) |