4.8 Article

Engineering injectable vascularized tissues from the bottom-up: Dynamics of in-gel extra-spheroid dermal tissue assembly

Journal

BIOMATERIALS
Volume 279, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2021.121222

Keywords

Biomaterial; Minimally invasive; Regenerative medicine

Funding

  1. FEDER (Fundo Europeu de Desenvolvimento Regional) through COMPETE 2020 - POCI, Portugal 2020 [POCI-01-0145-FEDER-028744, PTDC/BTMMAT/28744/2017]
  2. FCT (Fundacao para a Ciencia e a Tecnologia)
  3. FCT [IF/00296/2015, SFRH/BD/129855/2017]
  4. i3S Scientific Platform: Bioimaging member of the PPBI [PPBI-POCI-01-0145-FEDER-022122]
  5. i3S Scientific Platform: Bio-interfaces and Nanotechnology [UID/BIM/04293/2019]
  6. i3S Scientific Platform: In vivo CAM assays
  7. Fundação para a Ciência e a Tecnologia [SFRH/BD/129855/2017, UID/BIM/04293/2019] Funding Source: FCT

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Modular tissue engineering using spheroids as building blocks offers exciting possibilities for creating vascularized tissues from the bottom-up. A new injectable approach combining fibroblasts and endothelial progenitors has been developed to generate dense vascularized dermal tissue, showing promising results for clinical applications.
Modular tissue engineering approaches open up exciting perspectives for the biofabrication of vascularized tissues from the bottom-up, using micro-sized units such as spheroids as building blocks. While several techniques for 3D spheroid formation from multiple cell types have been reported, strategies to elicit the extraspheroid assembly of complex vascularized tissues are still scarce. Here we describe an injectable approach to generate vascularized dermal tissue, as an example application, from spheroids combining fibroblasts and endothelial progenitors (OEC) in a xeno-free (XF) setting. Short-term cultured spheroids (1 day) were selected over mature spheroids (7 days), as they showed significantly higher angiogenic sprouting potential. Embedding spheroids in fibrin was crucial for triggering cell migration into the external milieu, while providing a 3D framework for in-gel extra-spheroid morphogenesis. Migrating fibroblasts proliferated and produced endogenous ECM forming a dense tissue, while OEC self-assembled into stable capillaries with lumen and basal lamina. Massive in vitro interconnection between sprouts from neighbouring spheroids rapidly settled an intricate vascular plexus. Upon injection into the chorioallantoic membrane of chick embryos, fibrin-entrapped pre-vascularized XF spheroids developed into a macrotissue with evident host vessel infiltration. After only 4 days, perfused chimeric capillaries with human cells were present in proximal areas, showing fast and functional inosculation between host and donor vessels. This method for generating dense vascularized tissue from injectable building blocks is clinically relevant and potentially useful for a range of applications.

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