Human‐on‐Leaf‐Chip: A Biomimetic Vascular System Integrated with Chamber‐Specific Organs. Issue 22 (24th April 2020)

• Record Type: Journal Article
• Authors: Mao, Mao; Bei, Ho Pan; Lam, Chun Hei; Chen, Pengyu; Wang, Shuqi; Chen, Ying; He, Jiankang; Zhao, Xin
• Is Part Of: Small. Volume 16:Issue 22(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-04-24
• Subjects: cancer metastasis -- microfluidics -- organ‐on‐a‐chip -- vasculature; Nanotechnology -- Periodicals; Nanoparticles -- Periodicals; Microtechnology -- Periodicals; 620.5
• DOI: 10.1002/smll.202000546
• Languages: English
• ISSNs: 1613-6810

Abstract

Abstract: 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. Abstract : Organ‐on‐a‐chip technology is slowly maturing as studies begin to focus on establishing a vascular network to maintain organ‐to‐organ crosstalk and biomimetic variables. To integrate multiple vascularized organs in one human‐on‐leaf‐chip, chambers are edited in computer‐aided design of the highly efficient leaf venation network for multiple organ cultures. In this proof‐of‐concept, liver and bone are co‐cultured, which yields encouraging results.