AI Article Synopsis

  • Tissue engineering still faces challenges in developing a functional vascular network within engineered tissues, which is crucial for cell survival and metabolic activity.
  • A novel approach combines 3D-printed poly-ε-caprolactone scaffolds with a cell-accumulation technique, successfully doubling tissue thickness and enhancing scaffold handling and sample volume.
  • The study also highlights the relationship between increased pore sizes, vascular endothelial growth factor secretion under hypoxic conditions, and the formation of new vascular-like structures.

Article Abstract

A remaining challenge in tissue engineering approaches is the in vitro vascularization of engineered constructs or tissues. Current approaches in engineered vascularized constructs are often limited in the control of initial vascular network geometry, which is crucial to ensure full functionality of these constructs with regard to cell survival, metabolic activity, and potential differentiation ability. Herein, the combination of 3D-printed poly-ε-caprolactone scaffolds via melt electrospinning writing with the cell-accumulation technique to enable the formation and control of capillary-like network structures is reported. The cell-accumulation technique is already proven itself to be a powerful tool in obtaining thick (50 µm) tissues and its main advantage is the rapid production of tissues and its ease of performance. However, the applied combination yields tissue thicknesses that are doubled, which is of outstanding importance for an improved handling of the scaffolds and the generation of clinically relevant sample volumes. Moreover, a correlation of increasing vascular endothelial growth factor secretion to hypoxic conditions with increasing pore sizes and an assessment of the formation of neovascular like structures are included.

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http://dx.doi.org/10.1002/smll.201701521DOI Listing

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