Table 1.
Representative Skin Organoid Studies with Demonstrated in vivo Relevance to Wound Repair
| First Author (Year) |
Organoid Type/Structure | Cell Source | Key Fabrication/Culture Strategy | In vivo Model | Main Regenerative Outcomes |
|---|---|---|---|---|---|
| Diao et al6 | Sweat gland organoids | Mouse sweat gland epithelial cells |
3D culture of isolated sweat gland epithelial cells to form gland-like organoids |
Mouse full-thickness skin wounds and burned paw pads |
Accelerated wound closure and regenerated functional sweat glands |
| Lee et al8 | Human skin organoids with appendages |
hPSCs | TGF-β/BMP/FGF modulation combined with long-term 3D suspension culture |
Proof-of-concept model |
Generated epidermis, dermis and pigmented hair follicles, providing a platform for complex skin regeneration |
| Lee et al5 | Advanced appendage-forming skin organoids |
hPSCs | Optimized signaling cues and 3D culture to enhance appendage maturation |
Preclinical skin repair model |
Improved structural complexity and enhanced translational relevance |
| Kwak et al9 | Multilayered epidermal organoids |
iPSC-derived keratinocyte progenitors | 3D stratified epidermal culture and application of organoid secretome |
Full-thickness rodent wound |
Promoted re-epithelialization, collagen deposition and neovascularization |
| Wang et al7 | Neural-integrated skin organoids |
hPSC-derived skin organoids | Engineering of appendages and neural circuits followed by transplantation into defects |
Frostbite-induced full-thickness defects |
Improved healing compared with conventional therapy, enhanced appendage regeneration and reduced scarring |