Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/75314

TítuloMacromolecular modulation of a 3D hydrogel construct differentially regulates human stem cell tissue-to-tissue interface
Autor(es)Pereira, D. R.
Silva-Correia, J.
Oliveira, J. M.
Reis, R. L.
Pandit, A.
Palavras-chave3D hydrogels
Immune regeneration
INTERFACE
Stem cells
Tissue engineering
3D hydrogels stem cells
Interface tissue engineering
Data2022
EditoraElsevier
RevistaMaterials Science & Engineering: C
CitaçãoPereira D. R., Silva-Correia J., Oliveira J. M., Reis R. L., Pandit A. Macromolecular modulation of a 3D hydrogel construct differentially regulates human stem cell tissue-to-tissue interface, Materials Science & Engineering C, pp. 112611, doi:10.1016/j.msec.2021.112611, 2021
Resumo(s)The simultaneous generation of multiple tissues and their functional assembly into complex tissues remains a critical challenge for regenerative medicine. The tissue-to-tissue interface connecting two adjacent tissues is vital in effective tissue function. The presented worked hypothesize that differential functional property can be engineered by modulating the macromolecular composition of a 3D hydrogel construct and distinctively endow stem cell fate. Hence, it was possible to successfully generate macromolecular constructs by using the extracellular matrix (ECM)-based materials; type I collagen (Col I) and hyaluronic acid (HA); and natural-derived biomaterials as methacrylated gellan-gum (GGMA). The 3D hydrogel constructs consisted of two dissimilar layers: 1) Col I: HA hydrogel and 2) GGMA hydrogel. The tissue-to-tissue interface was created by seeding human mesenchymal stem cells (MSCs) between the two layers. Differential functional rheological and mechanical properties characterized the acellular 3D gradient hydrogel constructs. The cell-based 3D hydrogel constructs were assessed for MSCs viability by live/dead staining. Assessing apoptosis by flow cytometry, data showed the feasibility of the 3D hydrogel constructs in maintaining cell viability with no apoptosis induction onto MSCs. A homogeneous distribution was achieved in a successful cellular tissue-to-tissue interface. Human MSCs low proliferative rate and low ECM deposition were seen for all constructs; however, lower proliferative rate within the ECM microenvironment highlights controlled self-renewal of MSCs. The 3D hydrogel constructs maintained the human MSCs phenotype, yet the macromolecular modulation allowed tuning the human MSCs morphology from round to spindle-shaped phenotype. The intrinsic properties of the 3D cell-based hydrogel construct induced differential inflammatory and angiogenic paracrine secretory profiles owing to the dissimilar engineered biophysical milieu. Human MSCs sense the nearby macromolecular environment adjusting the cell-ECM interactions, which influence cell behaviour and fate. Beyond multi-tissue regeneration, the engineered cellular 3D hydrogel constructs may simultaneously address immune regeneration.
TipoArtigo
URIhttps://hdl.handle.net/1822/75314
DOI10.1016/j.msec.2021.112611
ISSN0928-4931
Versão da editorahttps://doi.org/10.1016/j.msec.2021.112611
Arbitragem científicayes
AcessoAcesso restrito UMinho
Aparece nas coleções:3B’s - Artigos em revistas/Papers in scientific journals

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