Hipster microcarriers: exploring geometrical and topographical cues of non-spherical microcarriers in biomedical applications

Detalhes bibliográficos
Autor(a) principal: Bjørge, Isabel M.
Data de Publicação: 2022
Outros Autores: Correia, Clara R., Mano, João F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/34624
Resumo: Structure and organisation are key aspects of the native tissue environment, which ultimately condition cell fate via a myriad of processes, including the activation of mechanotransduction pathways. By modulating the formation of integrin-mediated adhesions and consequently impacting cell contractility, engineered geometrical and topographical cues may be introduced to activate downstream signalling and ultimately control cell morphology, proliferation, and differentiation. Microcarriers appear as attractive vehicles for cell-based tissue engineering strategies aiming to modulate this 3D environment, but also as vehicles for cell-free applications, given the ease in tuning their chemical and physical properties. In this review, geometry and topography are highlighted as two preponderant features in actively regulating interactions between cells and the extracellular matrix. While most studies focus on the 2D environment, we focus on how the incorporation of these strategies in 3D systems could be beneficial. The techniques applied to design 3D microcarriers with unique geometries and surface topographical cues are covered, as well as specific tissue engineering approaches employing these microcarriers. In fact, successfully achieving a functional histoarchitecture may depend on a combination of fine-tuned geometrically shaped microcarriers presenting intricately tailored topographical cues. Lastly, we pinpoint microcarrier geometry as a key player in cell-free biomaterial-based strategies, and its impact on drug release kinetics, the production of steerable microcarriers to target tumour cells, and as protein or antibody biosensors.
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spelling Hipster microcarriers: exploring geometrical and topographical cues of non-spherical microcarriers in biomedical applicationsStructure and organisation are key aspects of the native tissue environment, which ultimately condition cell fate via a myriad of processes, including the activation of mechanotransduction pathways. By modulating the formation of integrin-mediated adhesions and consequently impacting cell contractility, engineered geometrical and topographical cues may be introduced to activate downstream signalling and ultimately control cell morphology, proliferation, and differentiation. Microcarriers appear as attractive vehicles for cell-based tissue engineering strategies aiming to modulate this 3D environment, but also as vehicles for cell-free applications, given the ease in tuning their chemical and physical properties. In this review, geometry and topography are highlighted as two preponderant features in actively regulating interactions between cells and the extracellular matrix. While most studies focus on the 2D environment, we focus on how the incorporation of these strategies in 3D systems could be beneficial. The techniques applied to design 3D microcarriers with unique geometries and surface topographical cues are covered, as well as specific tissue engineering approaches employing these microcarriers. In fact, successfully achieving a functional histoarchitecture may depend on a combination of fine-tuned geometrically shaped microcarriers presenting intricately tailored topographical cues. Lastly, we pinpoint microcarrier geometry as a key player in cell-free biomaterial-based strategies, and its impact on drug release kinetics, the production of steerable microcarriers to target tumour cells, and as protein or antibody biosensors.Royal Society of Chemistry2023-03-01T00:00:00Z2022-03-01T00:00:00Z2022-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/34624eng10.1039/D1MH01694FBjørge, Isabel M.Correia, Clara R.Mano, João F.info:eu-repo/semantics/embargoedAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T12:06:49Zoai:ria.ua.pt:10773/34624Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:05:52.424888Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Hipster microcarriers: exploring geometrical and topographical cues of non-spherical microcarriers in biomedical applications
title Hipster microcarriers: exploring geometrical and topographical cues of non-spherical microcarriers in biomedical applications
spellingShingle Hipster microcarriers: exploring geometrical and topographical cues of non-spherical microcarriers in biomedical applications
Bjørge, Isabel M.
title_short Hipster microcarriers: exploring geometrical and topographical cues of non-spherical microcarriers in biomedical applications
title_full Hipster microcarriers: exploring geometrical and topographical cues of non-spherical microcarriers in biomedical applications
title_fullStr Hipster microcarriers: exploring geometrical and topographical cues of non-spherical microcarriers in biomedical applications
title_full_unstemmed Hipster microcarriers: exploring geometrical and topographical cues of non-spherical microcarriers in biomedical applications
title_sort Hipster microcarriers: exploring geometrical and topographical cues of non-spherical microcarriers in biomedical applications
author Bjørge, Isabel M.
author_facet Bjørge, Isabel M.
Correia, Clara R.
Mano, João F.
author_role author
author2 Correia, Clara R.
Mano, João F.
author2_role author
author
dc.contributor.author.fl_str_mv Bjørge, Isabel M.
Correia, Clara R.
Mano, João F.
description Structure and organisation are key aspects of the native tissue environment, which ultimately condition cell fate via a myriad of processes, including the activation of mechanotransduction pathways. By modulating the formation of integrin-mediated adhesions and consequently impacting cell contractility, engineered geometrical and topographical cues may be introduced to activate downstream signalling and ultimately control cell morphology, proliferation, and differentiation. Microcarriers appear as attractive vehicles for cell-based tissue engineering strategies aiming to modulate this 3D environment, but also as vehicles for cell-free applications, given the ease in tuning their chemical and physical properties. In this review, geometry and topography are highlighted as two preponderant features in actively regulating interactions between cells and the extracellular matrix. While most studies focus on the 2D environment, we focus on how the incorporation of these strategies in 3D systems could be beneficial. The techniques applied to design 3D microcarriers with unique geometries and surface topographical cues are covered, as well as specific tissue engineering approaches employing these microcarriers. In fact, successfully achieving a functional histoarchitecture may depend on a combination of fine-tuned geometrically shaped microcarriers presenting intricately tailored topographical cues. Lastly, we pinpoint microcarrier geometry as a key player in cell-free biomaterial-based strategies, and its impact on drug release kinetics, the production of steerable microcarriers to target tumour cells, and as protein or antibody biosensors.
publishDate 2022
dc.date.none.fl_str_mv 2022-03-01T00:00:00Z
2022-03-01
2023-03-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/34624
url http://hdl.handle.net/10773/34624
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1039/D1MH01694F
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dc.publisher.none.fl_str_mv Royal Society of Chemistry
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