Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/178979
Title: Cellulose-based scaffolds enhance pseudoislets formation and functionality
Author: Velasco Mallorquí, Ferran
Rodríguez Comas, Júlia
Ramón Azcón, Javier
Keywords: Enginyeria de teixits
Materials biomèdics
Diabetis
Tissue engineering
Biomedical materials
Diabetes
Issue Date: 28-May-2021
Publisher: IOPscience
Abstract: In vitro research for the study of type 2 diabetes (T2D) is frequently limited by the availability of a functional model for islets of Langerhans. To overcome the limitations of obtaining pancreatic islets from different sources, such as animal models or human donors, immortalized cell lines as the insulin-producing INS1E β-cells have appeared as a valid alternative to model insulin-related diseases. However, immortalized cell lines are mainly used in flat surfaces or monolayer distributions, not resembling the spheroid-like architecture of the pancreatic islets. To generate islet-like structures, the use of scaffolds appeared as a valid tool to promote cell aggregations. Traditionally-used hydrogel encapsulation methods do not accomplish all the requisites for pancreatic tissue engineering, as its poor nutrient and oxygen diffusion induces cell death. Here, we use cryogelation technology to develop a more resemblance scaffold with the mechanical and physical properties needed to engineer pancreatic tissue. This study shows that carboxymethyl cellulose (CMC) cryogels prompted cells to generate β-cell clusters in comparison to gelatin-based scaffolds, that did not induce this cell organization. Moreover, the high porosity achieved with CMC cryogels allowed us to create specific range pseudoislets. Pseudoislets formed within CMC-scaffolds showed cell viability for up to 7 d and a better response to glucose over conventional monolayer cultures. Overall, our results demonstrate that CMC-scaffolds can be used to control the organization and function of insulin-producing β-cells, representing a suitable technique to generate β-cell clusters to study pancreatic islet function.
Note: Reproducció del document publicat a : https://doi.org/10.1088/1758-5090/ac00c3
It is part of: Biofabrication, 2021, vol 13, num. 3, p. 035044
URI: http://hdl.handle.net/2445/178979
Related resource: https://doi.org/10.1088/1758-5090/ac00c3
ISSN: 1758-5090
Appears in Collections:Articles publicats en revistes (Institut de Bioenginyeria de Catalunya (IBEC))

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