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. 2020 Oct 27;9(2):296–309. doi: 10.1016/j.gendis.2020.10.006

Table 1.

Comparison of MSC functions from different tissue sources.

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