TABLE 3.
Main characteristics of the seven studies included in the review on perichondrial stem/progenitor cells.
| Studies | Species of cells | Sorts of cells | Recipient animal | In vitro/in vitro | Scaffold | Definition of auricular cartilage differentiation | Conclusion |
|---|---|---|---|---|---|---|---|
| Derks et al. (2013) | Pig | ePPCs a , tPPCs b | Pig | In vitro | — | Histopathological examination (HE d , pentachrome, and alcian blue stain) and immunohistology (collagen type II) | Due to a high proliferative activity and a high chondrogenic capacity, ePPC might be a suitable cell source for cartilage tissue engineering |
| Kagimoto et al. (2016) | Monkey | PPCs c | Monkey/nude mouse | In vivo | — | Histopathological examination (Blyscan assay, HE, alcian blue, and Elastica van Gieson stain) and immunohistology (collagen type II) | The autologous transplantation of cartilage progenitors is potentially effective for reconstructing elastic cartilage |
| Oba et al. (2022) | Human | PPCs, ACCs | Nude mouse | In vivo | — | Histopathological examination (Blyscan assay, HE, alcian blue, and Elastica van Gieson stain) and immunohistology (collagen types I and II) | We succeeded in developing human auricular perichondrial chondroprogenitor cell-derived elastic cartilage in vitro that exhibits superficial effects when transplanted craniofacially, without major post-transplantation shrinkage |
| Togo et al. (2006) | Rabbit | PPCs, BMMSCs | Nude mouse | In vitro/vivo | Collagen sponge | Histopathological examination (toluidine blue and Elastica van Gieson) and and immunohistology (collagen type II) | Rabbit bone marrow mesenchymal stem cells used as controls could regenerate significantly smaller cartilage than perichondrocytes in the implant study |
| Xue et al. (2016) | Pig | PCCs, CSPCs | — | In vitro | — | Histopathological examination (toluidine blue) | We isolated cell populations from auricular cartilage and perichondrium and confirmed their stem cell properties by expression of stem cell surface marker, colony forming assay, and multiple differentiation potential |
| Zhang et al. (2019) | Pig | PCCs, CSPCs | — | In vitro | — | Histopathological examination (toluidine blue) | CSPCs showed a significant advantage in chondrogenesis in vivo with upregulated chondrogenic genes, a stable cartilage phenotype, and good mechanical properties |
| Otto et al. (2018) | Horse | BMMSCs, ACCs, PPCs | — | In vitro | GelMA hydrogel | Histopathological examination (HE and Safranin O/fast green) and immunohistology (collagen types I, II, and VI) | Although under the current culturing conditions, bone marrow-derived MSCs seemed to perform better in terms of matrix production, major advantages of ACPCs include the ability to generate high cell numbers, upregulation of the elastin gene, and a limited endochondral ossification potential |
ePPCs: ear perichondrial progenitor cells.
tPPCs: tracheal perichondrial progenitor cells.
PPCs: perichondrial progenitor cells.
HE: hematoxylin and eosin.