类有机物
生物医学工程
伤口愈合
再生医学
化学
干细胞
组织工程
微球
同轴
微载波
3d打印
细胞生物学
球体
细胞外基质
材料科学
基质(化学分析)
细胞培养
血管网
纳米技术
血管生成
三维细胞培养
自愈水凝胶
细胞
作者
K Wang,Lan Xiang,Jianwei Chen,Yu Wu,Delong Zhu,Xiangkai Kong,Ying Hu,Qian Liu,Kun Wang,Tao Xu,Lei Zhu
标识
DOI:10.1002/advs.202517409
摘要
Organoids are important tools for studying organ development, drug screening, and regenerative medicine, yet the absence of integrated vasculature limits their culture and translation. To address this, the PV-XOM strategy is proposed, which achieves one-step construction of pre-vascularized organoids through coaxial bioprinting: the inner phase uses temperature-responsive sacrificial material and endothelial cells to form hollow vascular channels, while the outer phase is a biomimetic hydrogel matrix containing organoid microspheres. Based on this framework, a pre-vascularized skin organoid model (PV-SOM) is established, in which the outer phase is loaded with adipose-derived stem cell (ADSC) microspheres and skin fibroblasts. In vitro, PV-SOM achieved rapid vascular closure and maturation; in vivo, it formed abundant neovessels in large skin defects, accelerated wound closure, and improved collagen remodeling. Proteomic analysis further revealed that ADSC microspheres activate the PI3K-AKT-mTOR pathway to regulate vascular formation across multiple stages. These findings show that PV-XOM offers an effective, scalable solution to the vascularization bottleneck of organoids with strong translational potential.
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