Vascularized skin tissue models featuring adipose cell spheroid-laden GelMA hydrogels
Lee D., Lee S., Lee J., Kim D., Kwon H., Ahn J.
Animal Study on Chronic Wound, Burns, published in Mater Today Bio (2025) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
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- Study type
- Animal Study
- Journal
- Mater Today Bio (2025)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 40469698
- PMCID
- PMC12136904
- DOI
- 10.1016/j.mtbio.2025.101835
Abstract (original English)
The multifaceted tissue interplay between skin and adipose structures is increasingly recognized to play crucial roles in antimicrobial defense, hair cycling, wound healing, and thermogenesis. However, the technical challenges associated with the development of an in vitro model of such complex tissues include the difficulties of integrating tissues with diverse characteristics. Here, we present a method using a gelatin methacryloyl (GelMA) hydrogel to establish a microenvironment that hosts connected composite tissues: a vascularized skin layer and a subcutaneous adipose layer. When adipogenesis proceeded in 3T3-L1 cell spheroid-laden three-dimensional (3D)-printed polycaprolactone (PCL) scaffolds after 1- and 2-min exposure to ultraviolet (UV) light, we observed that adipose tissue, the physical properties of which had been optimized by 1-min UV exposure, facilitated the migration and proliferation of 3T3-L1 cells. Furthermore, a notable enhancement in adipogenesis was apparent. Subsequently, using advanced 3D printing technology, we meticulously crafted a 3D vascularized skin layer by integrating microgels with human umbilical vein endothelial cells (HUVECs) and fibroblasts. HUVEC cells growing on the surface of the microgel exhibited a 3D structure that allowed vascular cells to become concentrated in the microgel area much more efficiently than in 2D culture. Three-dimensi
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is preclinical work; animal or laboratory results cannot be applied to humans.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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