Table 1.
English abbreviations | MSC source | Functional characteristics | References |
---|---|---|---|
BM-MSC | The bone marrow | Higher ability to differentiate into chondrocytes. The secretion group is rich in MFGE8; higher expression of TGF-β1, PGE2, and IL-6 than AD-MSC. |
20,23,27 |
AD-MSC | The adipose tissue | The proliferation rate is higher than BM-MSC. Higher ability to differentiate into adipocytes. Immunosuppression is stronger than that of BM-MSC. The immunogenicity is lower than that of BM-MSC, and the expressions of VEGF, HGF, Nestin and neurotrophic factor are higher. |
17,20,23 |
WJ-MSC | Wharton's jelly of umbilical cord | Compared with BM-MSC and AD-MSC, the proliferation potential and growth rate are higher, more passage potential in vitro, and the mitogen-induced T cell response is inhibited to a greater extent. | 18,25 |
UC-MSC | Human umbilical cord | Wider differentiation potential. Lower immunogenicity. The secreted group is rich in MFGE8, and does not express the tumor-related fibroblast phenotype. It has stronger angiogenic capacity than BM-MSC and AD-MSC, and higher expression of PGE2 and IL-6 than AD-MSC. |
7,17,23,26,27 |
Human embryo | Low immunogenicity. Not involved in proliferation. The secreted group do not contain MFGE8. |
17,27 | |
hAF-MSC | Human Amniotic fluid | Higher proliferation rate than MSC from adult source. The ability to differentiate more widely than that of an adult-derived MSC. Compared with MSC separated from dermal, it shares stem related miRNAs, but is significantly different from fat-forming miRNAs. |
7,17 |
The placenta | Less fat-forming potential. Good migration ability. |
7 | |
SHED | Human exfoliated deciduous teeth | Higher proliferation capacity than BM-MSC. Secretion group is rich in MFGE8. |
17,27 |