4.2 Article

Programming the Self-Organization of Endothelial Cells into Perfusable Microvasculature

Journal

TISSUE ENGINEERING PART A
Volume 29, Issue 3-4, Pages 80-92

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/ten.tea.2022.0072

Keywords

engineered tissues; engineered microvasculature; bioprinting; cell patterning; optimization; cell behavior; microenvironment; tissue morphogenesis; vasculogenesis

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The construction of three-dimensional microvascular networks remains challenging. In this study, we used bioprinting to pattern endothelial cells and investigated the microenvironmental cues necessary for their self-organization into microvessels. We found that the inclusion of fibrillar matrices and the absence of certain proteins in the culture medium promoted the formation of stable and perfusable microvascular networks in as little as 3 days.
The construction of three-dimensional (3D) microvascular networks with defined structures remains challenging. Emerging bioprinting strategies provide a means of patterning endothelial cells (ECs) into the geometry of 3D microvascular networks, but the microenvironmental cues necessary to promote their self-organization into cohesive and perfusable microvessels are not well known. To this end, we reconstituted microvessel formation in vitro by patterning thin lines of closely packed ECs fully embedded within a 3D extracellular matrix (ECM) and observed how different microenvironmental parameters influenced EC behaviors and their self-organization into microvessels. We found that the inclusion of fibrillar matrices, such as collagen I, into the ECM positively influenced cell condensation into extended geometries such as cords. We also identified the presence of a high-molecular-weight protein(s) in fetal bovine serum that negatively influenced EC condensation. This component destabilized cord structure by promoting cell protrusions and destabilizing cell-cell adhesions. Endothelial cords cultured in the presence of fibrillar collagen and in the absence of this protein activity were able to polarize, lumenize, incorporate mural cells, and support fluid flow. These optimized conditions allowed for the construction of branched and perfusable microvascular networks directly from patterned cells in as little as 3 days. These findings reveal important design principles for future microvascular engineering efforts based on bioprinting and micropatterning techniques. Impact statementBioprinting is a potential strategy to achieve microvascularization in engineered tissues. However, the controlled self-organization of patterned endothelial cells into perfusable microvasculature remains challenging. We used DNA Programmed Assembly of Cells to create cell-dense, capillary-sized cords of endothelial cells with complete control over their structure. We optimized the matrix and media conditions to promote self-organization and maturation of these endothelial cords into stable and perfusable microvascular networks.

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