TABLE 1.
Comparison of various properties of DMSCs (Guanlin et al., 2021; Linglu et al., 2021; Lu et al., 2020; Sabbagh et al., 2020; Al-Qadhi et al., 2021; Deng et al., 2024; Kotova et al., 2021; Nowwarote et al., 2020; Abe et al., 2022).
| Cellular type | Proliferation capacity | Differentiation potential | Immune regulation | Cell markers |
|---|---|---|---|---|
| DPSCs | The proliferation rate is similar to that of PDLSCs but lower than that of DFPCs. The proliferation capacity and osteoinductive ability are higher than those of DPSCs | Endothelial cells, osteoblasts, adipocytes, chondroprogenitor cells, hepatocytes and cardiomyocytes have neurogenic differentiation potential. Among them, the osteogenic differentiation ability is greater than that of DFPCs | It has immunomodulatory properties, can inhibit T cell proliferation, trigger M2 macrophage polarization, and suppress inflammation, etc. | Stro-1, CD49f, CD29, CD44、CD105, CD90 |
| SHEDs | The proliferation rate is similar to that of PDLSCs but lower than that of DFPCs. The proliferation capacity and osteoinductive ability are higher than those of DPSCs | Osteocytes, chondrocytes, adipocytes, odontoblasts, endothelial cells and hepatocytes Unique dental tissue and osteoinductive ability* Can be used as a neuroprotective agent* |
/ | CD73, CD90, CD105 CD146 |
| PDLSCs | / | The differentiation potential of osteocytes, endothelial cells, cardiomyocytes, islet-like cells and retinal ganglion-like cells It can form typical cementum and periodontal ligament-like structures |
/ | Stro-1, CD146, CD29, CD44, CD106 |
| GMSCs | Greater than PDLSCs, and the degree of senescence after continuous passage in vitro culture is less than that of PDLSCs. Compared with DPSCs and PDLSCs, it has a unique ability to automatically differentiate into gingiva in vivo | Neurogenic differentiation, adipocytes, chondrocytes and endothelial cells | / | CD13, CD29, CD44, CD54, CD73, CD90, CD105, CD166, Stro-1 |
Unique dental tissue and bone induction ability*: Capable of differentiating into odontoblasts and forming dentin-like or pulp-like tissues, rather than complete dentin-pulp-like complexes. In vivo, it recruits host osteoblasts to induce new bone formation, unlike in vitro where it differentiates into osteoblasts.
Can act as a neuroprotective agent*: Promotes neural function recovery through paracrine action and inhibits the formation of glial scars after spinal cord contusion.
Unique ability to automatically differentiate into gingiva in vivo*: Transplantation forms connective-like tissue expressing collagen I, a capability not possessed by DPSCs, and PDLSCs.
DPSCs, Dental pulp stem cells; SHEDs, Stem cells populations from human exfoliated deciduous teeth; PDLSCs, Periodontal ligament stem cells; GMSCs, Gingival mesenchymal stem cells; DFPCs, Dental follicle progenitor cells.