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* These authors contributed equally
This study introduces a novel κ-carrageenan sub-microgel suspension bath, displaying remarkable reversible jamming-unjamming transition properties. These attributes contribute to the construction of biomimetic tissues and organs in embedded 3D bioprinting. The successful printing of heart/esophageal-like tissues with high resolution and cell growth demonstrates high-quality bioprinting and tissue engineering applications.
Embedded three-dimensional (3D) bioprinting utilizing a granular hydrogel supporting bath has emerged as a critical technique for creating biomimetic scaffolds. However, engineering a suitable gel suspension medium that balances precise bioink deposition with cell viability and function presents multiple challenges, particularly in achieving the desired viscoelastic properties. Here, a novel κ-carrageenan gel supporting bath is fabricated through an easy-to-operate mechanical grinding process, producing homogeneous sub-microscale particles. These sub-microgels exhibit typical Bingham flow behavior with small yield stress and rapid shear-thinning properties, which facilitate the smooth deposition of bioinks. Moreover, the reversible gel-sol transition and self-healing capabilities of the κ-carrageenan microgel network ensure the structural integrity of printed constructs, enabling the creation of complex, multi-layered tissue structures with defined architectural features. Post-printing, the κ-carrageenan sub-microgels can be easily removed by a simple phosphate-buffered saline wash. Further bioprinting with cell-laden bioinks demonstrates that cells within the biomimetic constructs have a high viability of 92% and quickly extend pseudopodia, as well as maintain robust proliferation, indicating the potential of this bioprinting strategy for tissue and organ fabrication. In summary, this novel κ-carrageenan sub-microgel medium emerges as a promising avenue for embedded bioprinting of exceptional quality, bearing profound implications for the in vitro development of engineered tissues and organs.
Tissue engineering scaffolds, including electro-spun fibers, porous sponges, and polymer hydrogels, play a pivotal role in the repair and reconstruction of damaged tissues and organs by providing a structural framework supporting cell growth, tissue regeneration, and the restoration of organ function1,2,3. However, traditional scaffolds encounter challenges in accurately replicating native tissue structures, leading to a mismatch between the engineered and natural tissues. This limitation hinders the efficient healing of defective tissues, emphasizing the urgent need for scaf....
1. Preparation of the κ -carrageenan sub-microgel suspension bath
The granular κ-carrageenan gel bath was generated by mechanically breaking up the bulk hydrogels into a particulate gel slurry. The most recent study demonstrated that the κ-carrageenan particles exhibited an average diameter of approximately 642 ± 65 nm with uniform morphologies at 1000 rpm of mechanical blending15, significantly smaller than the dimensions of microgels previously reported in the literature16,17.......
The preparation of κ-carrageenan sub-microgel suspension baths for use in bioprinting is a carefully orchestrated process that involves several critical steps to ensure the resulting medium exhibits the desired properties for supporting bioinks. Initially, a κ-carrageenan solution is prepared by dissolving the κ-carrageenan powder in deionized water at elevated temperatures, creating a homogeneous mixture. The concentration of th.......
This research was supported by Ningbo Natural Science Foundation (2022J121, 2023J159), Key project of Natural Science Foundation of Ningbo City (2021J256), Open Foundation of the State Key Laboratory of Molecular Engineering of Polymers (Fudan University) (K2024-35), and Key Laboratory of Precision Medicine for Atherosclerotic Diseases of Zhejiang Province, China (2022E10026). Thanks for the technical support by the Core Facilities, Health Science Center of Ningbo University.
....Name | Company | Catalog Number | Comments |
3D bioprinter | Custom-designed | ||
4’,6-Diamidino-2-Phenylindole | Solarbio Life Science | C0065 | Ready-to-use |
405 nm UV light | EFL | XY-WJ01 | |
Cell Counter | Corning | Cyto smart 6749 | |
Confocal laser scanning microscope | Leica | STELLARIS 5 | |
DMEM high glucose | VivaCell | C3113-0500 | High Glucose, with Sodium Pyruvate and L-Glutamine |
Dynamic rotational rheometer | TA Instrument | Discovery HR-20 | |
Esophageal smooth muscle cells | Supplied by the Department of Cell Biology and Regenerative Medicine, Health Science Center, Ningbo University | Primary cells from the rabbit esophagus | |
Fetal bovine serum | UE | F9070L | |
Fluorescein isothiocyanate labeled phalloidin | Solarbio Life Science | CA1610 | 300T |
Gelatin methacrylate | EFL | EFL-GM-60 | 60% substitution |
k-carrageenan | Aladdin | C121013-100g | Reagent grade |
Lithium Phenyl (2,4,6-trimethylbenzoyl) phosphinate | Aladdin | L157759-1g | 365~405 nm |
Live-Dead kit | beyotime | C2015M | |
Microplate reader | Potenov | PT-3502B | |
Paraformaldehyde | Solarbio Life Science | P1110 | 4% |
Penicillin/streptomycin | Solarbio Life Science | MA0110 | 100 ´ |
Phosphate buffered saline | VivaCell | C3580-0500 | pH 7.2-7.4 |
Silk fibroin methacrylate | EFL | EFL-SilMA-001 | 39% substitution |
Triton X-100 | Solarbio Life Science | T8200 | |
Trypsin-EDTA | VivaCell | C100C1 | 0.25%, without phenol red |
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