3D Bioprinting of Collagen-based Microfluidics for Engineering Fully-biologic Tissue Systems.
Daniel J ShiwarskiAndrew R HudsonJoshua W TashmanEzgi BakirciSamuel MossBrian D CoffinAdam W FeinbergPublished in: bioRxiv : the preprint server for biology (2024)
Microfluidic and organ-on-a-chip devices have improved the physiologic and translational relevance of in vitro systems in applications ranging from disease modeling to drug discovery and pharmacology. However, current manufacturing approaches have limitations in terms of materials used, non-native mechanical properties, patterning of extracellular matrix (ECM) and cells in 3D, and remodeling by cells into more complex tissues. We present a method to 3D bioprint ECM and cells into microfluidic collagen-based high-resolution internally perfusable scaffolds (CHIPS) that address these limitations, expand design complexity, and simplify fabrication. Additionally, CHIPS enable size-dependent diffusion of molecules out of perfusable channels into the surrounding device to support cell migration and remodeling, formation of capillary-like networks, and integration of secretory cell types to form a glucose-responsive, insulin-secreting pancreatic-like microphysiological system.
Keyphrases
- extracellular matrix
- induced apoptosis
- cell cycle arrest
- high resolution
- single cell
- drug discovery
- high throughput
- circulating tumor cells
- tissue engineering
- endoplasmic reticulum stress
- rheumatoid arthritis
- mass spectrometry
- mesenchymal stem cells
- insulin resistance
- signaling pathway
- oxidative stress
- wound healing
- liquid chromatography
- cell fate