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Background <p>Inadequate vascularization remains a major limitation in tissue engineering, often leading to graft failure due to limited oxygen and nutrient supply. Prevascularization, the formation of microvascular networks within scaffolds before implantation, aims to accelerate perfusion and improve graft integration. We developed bilayer electrospun poly(ε-caprolactone)/poly(l-lactide) (PCL/PLA) scaffolds prevascularized by co-culture of human adipose-derived mesenchymal stem cells (AD-MSCs) and human placental arterial endothelial cells (HPAECs).</p> Methods <p>AD-MSCs were isolated from lipoaspirates and characterized by flow cytometry and functional assays. Bilayered PCL/PLA scaffolds were engineered with a wide-meshed layer for cell infiltration and a fine-meshed layer for mechanical stability. Scaffolds were seeded with AD-MSCs, HPAECs, or both (co-culture). Cell viability, adhesion, and apoptosis were analyzed histologically. Angiogenic and vasculogenic potential was evaluated in vitro and in vivo using the chick chorioallantoic membrane (CAM) assay.</p> Results <p>AD-MSCs expressed characteristic markers, demonstrated adipogenic and osteogenic differentiation, and promoted angiogenesis in 2D co-culture. ELISA analyses indicated dynamic secretion of VEGF, HGF, and bFGF, reflecting both paracrine and contact-dependent AD-MSC–HPAEC interactions. On scaffolds, cells primarily adhered to the wide-meshed layer. Co-culture induced vessel-like structures within a multicellular stromal environment; monocultures did not support prevascularization. Five days post-implantation, prevascularized scaffolds exhibited human microvessels at the scaffold–CAM interface and in adjacent tissue, closely associated with AD-MSCs and containing chicken erythrocytes—indicating successful anastomosis and functional perfusion. Quantitative analysis showed a significant increase in vessel branching points in the host CAM tissue in response to AD-MSC-only (2.8-fold) and co-culture (3.5-fold) scaffolds versus acellular controls (<i>p</i> &lt; 0.05). HPAEC-only scaffolds did not promote vascular outgrowth, likely due to poor cell survival.</p> Conclusion <p>Scaffolds seeded with AD-MSCs enhanced host angiogenesis, while only co-cultures with HPAECs supported scaffold prevascularization and functional vascular integration in vivo. The stromal–endothelial combination enabled formation of perfused human microvessels and promoted host vascular remodeling. These findings underscore the translational potential of prevascularized, electrospun scaffolds for improving graft survival in ischemic or poorly vascularized environments.</p>

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Prevascularization of electrospun PCL/PLA scaffolds using human adipose-derived stem and endothelial cells enhances vascular integration and host angiogenesis in vivo

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年5月20日

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  • Lavinia Grob,
  • Dagmar Brislinger,
  • Marc Mueller,
  • Anja Högler,
  • Kathrin Galistl,
  • Monika Sundl,
  • Daniel Kummer,
  • Nassim Ghaffari-Tabrizi-Wizsy,
  • Hannah Müller,
  • Melanie Pichlsberger,
  • Lars-Peter Kamolz,
  • Ingrid Lang-Olip

摘要

Background

Inadequate vascularization remains a major limitation in tissue engineering, often leading to graft failure due to limited oxygen and nutrient supply. Prevascularization, the formation of microvascular networks within scaffolds before implantation, aims to accelerate perfusion and improve graft integration. We developed bilayer electrospun poly(ε-caprolactone)/poly(l-lactide) (PCL/PLA) scaffolds prevascularized by co-culture of human adipose-derived mesenchymal stem cells (AD-MSCs) and human placental arterial endothelial cells (HPAECs).

Methods

AD-MSCs were isolated from lipoaspirates and characterized by flow cytometry and functional assays. Bilayered PCL/PLA scaffolds were engineered with a wide-meshed layer for cell infiltration and a fine-meshed layer for mechanical stability. Scaffolds were seeded with AD-MSCs, HPAECs, or both (co-culture). Cell viability, adhesion, and apoptosis were analyzed histologically. Angiogenic and vasculogenic potential was evaluated in vitro and in vivo using the chick chorioallantoic membrane (CAM) assay.

Results

AD-MSCs expressed characteristic markers, demonstrated adipogenic and osteogenic differentiation, and promoted angiogenesis in 2D co-culture. ELISA analyses indicated dynamic secretion of VEGF, HGF, and bFGF, reflecting both paracrine and contact-dependent AD-MSC–HPAEC interactions. On scaffolds, cells primarily adhered to the wide-meshed layer. Co-culture induced vessel-like structures within a multicellular stromal environment; monocultures did not support prevascularization. Five days post-implantation, prevascularized scaffolds exhibited human microvessels at the scaffold–CAM interface and in adjacent tissue, closely associated with AD-MSCs and containing chicken erythrocytes—indicating successful anastomosis and functional perfusion. Quantitative analysis showed a significant increase in vessel branching points in the host CAM tissue in response to AD-MSC-only (2.8-fold) and co-culture (3.5-fold) scaffolds versus acellular controls (p < 0.05). HPAEC-only scaffolds did not promote vascular outgrowth, likely due to poor cell survival.

Conclusion

Scaffolds seeded with AD-MSCs enhanced host angiogenesis, while only co-cultures with HPAECs supported scaffold prevascularization and functional vascular integration in vivo. The stromal–endothelial combination enabled formation of perfused human microvessels and promoted host vascular remodeling. These findings underscore the translational potential of prevascularized, electrospun scaffolds for improving graft survival in ischemic or poorly vascularized environments.