4.8 Article

Human-on-Leaf-Chip: A Biomimetic Vascular System Integrated with Chamber-Specific Organs

Journal

SMALL
Volume 16, Issue 22, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202000546

Keywords

cancer metastasis; microfluidics; organ-on-a-chip; vasculature

Funding

  1. General Research Fund from the Hong Kong Research Grants Council [15202119]
  2. Intra-faculty fund (ZVPC) from the Hong Kong Polytechnic University
  3. Guangdong Provincial Key Laboratory of Functional Soft Condensed Matter, National Key R&D Program of China [2016YFC1101302, 2018YFA0703000]
  4. National Natural Science Foundation of China [31871016, 51675412, 51422508]
  5. Key Research Project of Shaanxi Province [2017ZDXM-GY-058]
  6. Youth Innovation Team of Shaanxi Universities
  7. Fundamental Research Funds for the Central Universities
  8. National Key Scientific Instrument and Equipment Development Projects from the National Natural Science Foundation of China [61827806]
  9. Germany/HK Joint Research Scheme from the Hong Kong Research Grants Council [G-PolyU508/18]

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The vascular network is a central component of the organ-on-a-chip system to build a 3D physiological microenvironment with controlled physical and biochemical variables. Inspired by ubiquitous biological systems such as leaf venation and circulatory systems, a fabrication strategy is devised to develop a biomimetic vascular system integrated with freely designed chambers, which function as niches for chamber-specific vascularized organs. As a proof of concept, a human-on-leaf-chip system with biomimetic multiscale vasculature systems connecting the self-assembled 3D vasculatures in chambers is fabricated, mimicking the in vivo complex architectures of the human cardiovascular system connecting vascularized organs. Besides, two types of vascularized organs are built independently within the two halves of the system to verify its feasibility for conducting comparative experiments for organ-specific metastasis studies in a single chip. Successful culturing of human hepatoma G2 cells (HepG2s) and mesenchymal stem cells (MSCs) with human umbilical vein endothelial cells (HUVECs) shows good vasculature formation, and organ-specific metastasis is simulated through perfusion of pancreatic cancer cells and shows distinct cancer encapsulation by MSCs, which is absent in HepG2s. Given good culture efficacy, study design flexibility, and ease of modification, these results show that the bioinspired human-on-leaf-chip possesses great potential in comparative and metastasis studies while retaining organ-to-organ crosstalk.

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