Advanced Binary Guanosine and Guanosine 5'‑Monophosphate Cell-Laden Hydrogels for Soft Tissue Reconstruction by 3D Bioprinting [Dataset]

Soft tissue defects or pathologies frequently necessitate the use of biomaterials that provide the volume required for subsequent vascularization and tissue formation as autrografts are not always a feasible alternative. Supramolecular hydrogels represent promising candidates because of their 3D str...

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Detalles Bibliográficos
Autores: Godoy-Gallardo, María, Merino-Gómez, Maria, Mateos-Timoneda, Miguel A., Eckhard, Ulrich, Gil, Francisco Javier, Pérez, Román A.
Tipo de recurso: conjunto de datos
Estado:Versión publicada
Fecha de publicación:2023
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/356211
Acceso en línea:http://hdl.handle.net/10261/356211
Access Level:acceso abierto
Palabra clave:Thereby potentially improving
sup >+
Recent years since
Present work aimed
Native extracellular matrix
Indicating successful differentiation
Indicating excellent g
Extensive nanofibrillar network
Evenly distributed throughout
Tissue reconstruction intervention
Soft tissue reconstruction
Providing enough stability
Low shape stability
Proper cell functioning
Pathologies frequently necessitate
Lipid droplet formation
Hydrogels may enable
Ensure scaffold biointegration
3d printing due
Binary hydrogel made
Laden hydrogel capable
Sustain living cells
Ensuring cell survival
Advanced binary guanosine
Binary cell
Tissue formation
Hydrogel scaffold
Cell survival
Laden hydrogels
Increase stability
Frequently inappropriate
Quadruplex formation
Printed scaffold
Based hydrogels
3d structure
3d bioprinting
Volume required
Ultimately forming
Thixotropic qualities
Subsequent vascularization
Printed structure
Prime candidates
Nucleoside self
Material spreading
Hyperbranched polyethylenimine
Feasible alternative
Coordinating k
Adipogenic conditions
7 days
21 days
2000 kda
Descripción
Sumario:Soft tissue defects or pathologies frequently necessitate the use of biomaterials that provide the volume required for subsequent vascularization and tissue formation as autrografts are not always a feasible alternative. Supramolecular hydrogels represent promising candidates because of their 3D structure, which resembles the native extracellular matrix, and their capacity to entrap and sustain living cells. Guanosine-based hydrogels have emerged as prime candidates in recent years since the nucleoside self-assembles into well-ordered structures like G-quadruplexes by coordinating K+ ions and π–π stacking, ultimately forming an extensive nanofibrillar network. However, such compositions were frequently inappropriate for 3D printing due to material spreading and low shape stability over time. Thus, the present work aimed to develop a binary cell-laden hydrogel capable of ensuring cell survival while providing enough stability to ensure scaffold biointegration during soft tissue reconstruction. For that purpose, a binary hydrogel made of guanosine and guanosine 5'-monophosphate was optimized, rat mesenchymal stem cells were entrapped, and the composition was bioprinted. To further increase stability, the printed structure was coated with hyperbranched polyethylenimine. Scanning electron microscopic studies demonstrated an extensive nanofibrillar network, indicating excellent G-quadruplex formation, and rheological analysis confirmed good printing and thixotropic qualities. Additionally, diffusion tests using fluorescein isothiocyanate labeled-dextran (70, 500, and 2000 kDa) showed that nutrients of various molecular weights may diffuse through the hydrogel scaffold. Finally, cells were evenly distributed throughout the printed scaffold, cell survival was 85% after 21 days, and lipid droplet formation was observed after 7 days under adipogenic conditions, indicating successful differentiation and proper cell functioning. To conclude, such hydrogels may enable the 3D bioprinting of customized scaffolds perfectly matching the respective soft tissue defect, thereby potentially improving the outcome of the tissue reconstruction intervention.