3D Human iPSC Blood Vessel Organoids as a Source of Flow-Adaptive Vascular Cells for Creating a Human-Relevant 3D-Scaffold Based Macrovessel Model
Meijer, Elana M; Koch, Suzanne E; van Dijk, Christian G M; Maas, Renee G C; Chrifi, Ihsan; Szymczyk, Wojciech; Besseling, Paul J; Pomp, Lisa; Koomen, Vera J C H; Buikema, Jan Willem; Bouten, Carlijn V C; Verhaar, Marianne C; Smits, Anthal I P M; Cheng, Caroline
(2023) Advanced Biology, volume 7, issue 1
(Article)
Abstract
3D-scaffold based in vitro human tissue models accelerate disease studies and screening of pharmaceutics while improving the clinical translation of findings. Here is reported the use of human induced pluripotent stem cell (hiPSC)-derived vascular organoid cells as a new cell source for the creation of an electrospun polycaprolactone-bisurea (PCL-BU) 3D-scaffold-based,
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perfused human macrovessel model. A separation protocol is developed to obtain monocultures of organoid-derived endothelial cells (ODECs) and mural cells (ODMCs) from hiPSC vascular organoids. Shear stress responses of ODECs versus HUVECs and barrier function (by trans endothelial electrical resistance) are measured. PCL-BU scaffolds are seeded with ODECs and ODMCs, and tissue organization and flow adaptation are evaluated in a perfused bioreactor system. ODECs and ODMCs harvested from vascular organoids can be cryopreserved and expanded without loss of cell purity and proliferative capacity. ODECs are shear stress responsive and establish a functional barrier that self-restores after the thrombin challenge. Static bioreactor culture of ODECs/ODMCs seeded scaffolds results in a biomimetic vascular bi-layer hierarchy, which is preserved under laminar flow similar to scaffolds seeded with primary vascular cells. HiPSC-derived vascular organoids can be used as a source of functional, flow-adaptive vascular cells for the creation of 3D-scaffold based human macrovascular models.
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Keywords: blood vessel organoids, endothelial cells, graft perfusion, vascular graft, vasculature, General Biochemistry,Genetics and Molecular Biology, Biomedical Engineering, Biomaterials, Journal Article
ISSN: 2701-0198
Publisher: John Wiley & Sons Inc.
Note: Funding Information: The authors would like to thank Rob Driessen for his help with the flow pump system and the critical point dryer. In addition, the authors would like to thank Krista den Ouden for her help with sectioning and staining of the 3D samples. This work was funded by the REGMEDXB cardiovascular moonshot consortium, the NWO vidi grant (no. 91714302 to CC), the TKI Health Holland BIORAB project (no. LSHM19032), and the InSiTeVx project (436001003), which is financially supported by ZonMw within the LSH 2Treat Program and the Dutch Kidney Foundation. The authors gratefully acknowledge the Gravitation Program “Materials Driven Regeneration”, funded by the Netherlands Organization for Scientific Research (024.003.013). Publisher Copyright: © 2022 The Authors. Advanced Biology published by Wiley-VCH GmbH.
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