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. 2021 Jul 23;9:654210. doi: 10.3389/fcell.2021.654210

TABLE 9.

Studies regarding mesenchymal stromal cell-conditioned medium for skin rejuvenation in animal models.

MSC source Method of tissue extraction MSC characterization MSC treatment Model Groups of treatments and via of administration Follow-up (days) Assessment Main outcomes
Zhang K. et al., 2020 Human umbilical cord Umbilical cord dissection Western blotting (CD9+, CD63+, CD81+, and calnexin−) MSC-CMs of passage 6 at 80–90% confluence were used. CM was collected, and Exos were obtained Murine. Photoaged mouse model - Control (non-photoaged mouse)
- SHS-PBS
- Exos
- SHS-Exos (n = 6/group)
14 Macroscopic appearance, microscopic appearance (microwrinkles analysis), histology, and qRT-PCR SHS-Exos reduced microwrinkles, alleviated histopathological changes, and promoted the expression of extracellular matrix constituents, while Exos alone produced weaker effects
Kwon et al., 2016 Human bone marrow from the posterior iliac crest Aspiration Flow cytometry (CD73+, CD105+, CD14−, CD34−, CD45−) MSCs of passage 6 at 80% confluence were used and cultured in hypoxic conditions. CM was then collected Murine. UVB-irradiated mice model 200 μl of treatment topically applied three times a week
- Vehicle solution (polyethylene glycol:ethanol)
- Adenosine 0.04%
- MSC-CM 1%
- MSC-CM 10% (n = 8/group)
56 Macroscopic appearance (photography, visual skin grading), tape stripping, biophysical measurements (TEWL and hydration), histology (HE, IHC) The MSC-CM group exhibited significantly reduced levels of total wrinkle area compared with the vehicle-treated group. TEWL levels decreased while hydration increased in MSC-CM
Ueda and Nishino, 2010 Human dental pulp tissue Healthy permanent deciduous teeth extraction MSCs of passage 1 to 3 were used, and CM was collected Murine. Wrinkled mice induced by UVB Subcutaneous injections
- MSC-CM
- MSCs
- PBS (n = 8/group)
35 Macroscopic appearance (photography, histology (HE) MSCs and MSC-CM decreased wrinkles more than the PBS group. The greatest effect was observed in MSC group. Measurement of the dermal thickness showed significant increases in MSC and MSC-CM groups

CM, conditioned medium; Exos, exosomes; HE, hematoxylin and eosin; IHC, immunohistochemistry; MSCs, mesenchymal stromal cells; MT, Masson’s trichrome; PBS, phosphate-buffered saline; qRT-PCR, real-time quantitative polymerase chain reaction; SHSs, sponge Haliclona sp. spicules; TEWL, transepidermal water loss.