4.5 Review

Organ-on-a-chip systems for vascular biology

期刊

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.yjmcc.2021.06.002

关键词

Vascular biology; Organ-on-a-chip; Endothelial cells; Organoids; Microfluidics; Mechanotransduction

资金

  1. National Institute of Health [R01 HL141570, UH2/UH3 DK107343, 1R01AI148802, R01 AI141602, F32 HL143949]
  2. United Therapeutics Jenesis Innovative Research Award
  3. National Science Foundation Graduate Student Research Fellowship [DGE 1762114]
  4. Institute of Stem Cell and Regenerative Medicine at the University of Washington

向作者/读者索取更多资源

Organ-on-a-chip platforms involve miniaturization of cell culture systems, enabling novel experimental approaches such as modeling biophysical forces on cells and screening new drugs. Vascular structure is a key feature in these systems, with recent advances focusing on developing vascular models for studying vascular biology and tissue regeneration. Future approaches aim to select fit-for-purpose OOC models to either serve as simple testbeds for therapeutic development or accurately replicate human physiology for specific disease modeling and tissue regeneration.
Organ-on-a-chip (OOC) platforms involve the miniaturization of cell culture systems and enable a variety of novel experimental approaches. These range from modeling the independent effects of biophysical forces on cells to screening novel drugs in multi-organ microphysiological systems, all within microscale devices. As in living systems, the incorporation of vascular structure is a key feature common to almost all organ-on-a-chip systems. In this review we highlight recent advances in organ-on-a-chip technologies with a focus on the vasculature. We first present the developmental process of the blood vessels through which vascular cells assemble into networks and remodel to form complex vascular beds under flow. We then review self-assembled vascular models and flow systems for the study of vascular development and biology as well as pre-patterned vascular models for the generation of perfusable microvessels for modeling vascular and tissue function. We finally conclude with a perspective on developing future OOC approaches for studying different aspects of vascular biology. We highlight the fit for purpose selection of OOC models towards either simple but powerful testbeds for therapeutic development, or complex vasculature to accurately replicate human physiology for specific disease modeling and tissue regeneration.

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