4.6 Review Book Chapter

Engineering Vascularized Organoid-on-a-Chip Models

Journal

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev-bioeng-090120-094330

Keywords

vasculogenesis; angiogenesis; self-assembled vasculature; microphysiological systems; organ-on-a-chip; tumor-on-a-chip

Funding

  1. US National Institutes of Health [UG3/UH3 HL141800, UG3DK122639]
  2. Translational Research Institute for Space Health (TRISH) [FIP-58]
  3. Cancer Research Coordinating Committee of the University of California system [C21CR2153]
  4. Chao Family Comprehensive Cancer Center through National Cancer Institute Center [P30A062203]
  5. [UG3/UH3 TR002137]
  6. [U54 CA217378]

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The technology of vascularized organoids is rapidly advancing, with the key goal of reproducing specific organ functions and simulating tumor progression. Vascularization is not only a critical component of individual organ function, but also responsible for linking the fate of all organs and their functions.
Recreating human organ-level function in vitro is a rapidly evolving field that integrates tissue engineering, stem cell biology, and microfluidic technology to produce 3D organoids. A critical component of all organs is the vasculature. Herein, we discuss general strategies to create vascularized organoids, including common source materials, and survey previous work using vascularized organoids to recreate specific organ functions and simulate tumor progression. Vascularization is not only an essential component of individual organ function but also responsible for coupling the fate of all organs and their functions. While some success in coupling two or more organs together on a single platform has been demonstrated, we argue that the future of vascularized organoid technology lies in creating organoid systems complete with tissue-specific microvasculature and in coupling multiple organs through a dynamic vascular network to create systems that can respond to changing physiological conditions.

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