The Impact of Channel Geometry and Flow Regime on Endothelial Orientation and Morphology in Vessel-on-Chip

Mohammad Jouybar, Sophie R. van der Kallen, Sheen Sahebali, Carlijn V.C. Bouten, Jaap M.J. den Toonder (Corresponding author)

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Abstract

This study investigates the impact of channel geometry and applied flow on the orientation and morphology of endothelial cells (ECs) within vessel-on-chip (VoC) models. Traditional organ-on-chip models often utilize rectangular cross-section channels, resulting in flat walls, sharp corners, and non-uniform wall shear stress profiles, which do not accurately mimic physiological conditions. Tubular channels with circular cross-sections provide a more in vivo-like geometry and result in a physiological uniform wall shear stress. Here, tubular channels fabricated using sugar 3D-printing are compared with rectangular channels made via stereolithography 3Dprinting. The results show that ECs from both blood and lymph vessels exhibit more uniform coverage and circumferential alignment in tubular channels than in rectangular channels. Unidirectional or bidirectional flow conditions align ECs parallel to the flow, overruling the circumferential alignment induced by curvature in tubular channels. Pulsatile flow enhances circumferential orientation in tubular channels, while alignment along the flow is maintained in rectangular channels. Additionally, EC orientation induced by flow impacts monocyte rolling velocities, crucial for understanding immune cell motility. This study underlines the importance of the combined effect of channel geometry and flow conditions in VoC models, and advocates for the continued development of advanced organ-on-chip systems that better replicate human physiology.
Original languageEnglish
Article number2401994
Number of pages19
JournalAdvanced Materials Technologies
Volume10
Issue number7
Early online date12 Feb 2025
DOIs
Publication statusPublished - 4 Apr 2025

Funding

This work was supported by the Institute of Complex Molecular Systems (ICMS), the European project Moore4Medical [10028031], and by the Dutch Research Council NWO (grant number Science-XL 2019.022, \u2018The Active Matter Physics of Collective Metastasis'). Moore4Medical has received funding within the Electronic Components and Systems for European Leadership Joint Undertaking (ECSEL JU) in collaboration with the European Union's H2020 Framework Programme (H2020/2014-2020) and National Authorities, under grant agreement H2020-ECSEL-2019-IA-876190 www.moore4medical.eu. Furthermore, this research was performed within the framework of CTMM, the Center for Translational Molecular Medicine (www.ctmm.nl), project CIRCULATING CELLS (grant 01C-102), and supported by the Dutch Heart Foundation. The authors declare no competing financial\u00A0interests. This work was supported by the Institute of Complex Molecular Systems (ICMS), the European project Moore4Medical [10028031], and by the Dutch Research Council NWO (grant number Science\u2010XL 2019.022, \u2018The Active Matter Physics of Collective Metastasis'). Moore4Medical has received funding within the Electronic Components and Systems for European Leadership Joint Undertaking (ECSEL JU) in collaboration with the European Union's H2020 Framework Programme (H2020/2014\u20102020) and National Authorities, under grant agreement H2020\u2010ECSEL\u20102019\u2010IA\u2010876190 www.moore4medical.eu . Furthermore, this research was performed within the framework of CTMM, the Center for Translational Molecular Medicine (www.ctmm.nl), project CIRCULATING CELLS (grant 01C\u2010102), and supported by the Dutch Heart Foundation. The authors declare no competing financial interests.

Keywords

  • vessel-on-chip
  • vessel morphology
  • vessel flow
  • sugar 3D-printing
  • organ-on-chip
  • monocyte rolling

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