Magnetic responsive cell-based platforms for tissue engineering applications
Main Author: | |
---|---|
Publication Date: | 2023 |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | http://hdl.handle.net/10773/38207 |
Summary: | The major goal of tissue engineering consists on the development of biological substitutes to repair or replace damaged tissues. However, the fabrication of clinically relevant tissue replacements is still illusory, hampering their transactional to clinical practices. During the design of tissues in vitro, all the functional and morphological features must be recapitulated. To address this challenge, scaffold-free approaches have emerged as powerful strategies for the fabrication of tissue constructs with enhanced deposition of extracellular matrix, essential for the natural development of the tissue architecture. Nevertheless, the traditional approaches still fail on engineering tissues with high level of complexity, as seen in stratified and hierarchical conformations, as well with adequate mechanical performance. Therefore, this PhD proposal aimed to develop improved tissue substitutes that closely mimic key functional aspects of the native microenvironment. By using magnetized cells as basic living units, we propose the fabrication of magnetic membranes of cells through magnetic force-based tissue engineering (Mag-TE). The magnetic character of the created tissues allowed a precise control over cells’ positioning and, consequently, an extremely guided-assembling of the tissues. Following this strategy, cohesive and robust macrotissues with enhanced mechanical behavior were fabricated, circumventing one of the major limitations of scaffold-free approaches which includes the development of mechanically weak tissue constructs. Concerning the architecture of the native tissues, magnetic living substitutes with intricate geometries were developed, attesting the versatility of this approach. Another problematic regarding the development of tissue substitutes is the lack of adequate diffusion of nutrients and oxygen, which may lead to premature cell death. To overcome this obstacle, we engineered pre-vascularized multilayered cell sheets, exhibiting preserved human vascular structures and the ability to integrate the host vasculature. In this thesis, small tissue units at the microscale were also designed through the combination of Mag-TE and a high-throughput platform. These microtissues could further act as living building blocks for the fabrication of larger heterotypic tissue constructs or as in vitro platforms for disease modelling and drug screening. Finally, by exploring the magnetic character of our improved living tissues, we evaluated the role of magnetic field on modulating the cell fate of tissues produced in vitro. Upon magnetic stimulation, we triggered the osteogenic differentiation of the magnetized tissues, opening new possibilities for advanced strategies in bone regeneration. Using an in vivo mice model, we were also able to stimulate tissue integration and the osteogenic differentiation of the implant in situ. By using magnetized cells as building materials, we envisaged the fabrication of complex multiscale and multifunctional tissues with clinical relevance. The magnetic features of the designed tissues could accelerate the translation of Mag-TE to the clinical practices, allowing the remote and in situ guiding of implants into the expected tissue function, while guarantying a feasible monitoring and tracking along the time. |
id |
RCAP_4a0fb57c870e3d00e5d8fe37a721b746 |
---|---|
oai_identifier_str |
oai:ria.ua.pt:10773/38207 |
network_acronym_str |
RCAP |
network_name_str |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
repository_id_str |
https://opendoar.ac.uk/repository/7160 |
spelling |
Magnetic responsive cell-based platforms for tissue engineering applicationsCell sheetMagnetic fieldMechanotransductionStem cellsTissue engineeringThe major goal of tissue engineering consists on the development of biological substitutes to repair or replace damaged tissues. However, the fabrication of clinically relevant tissue replacements is still illusory, hampering their transactional to clinical practices. During the design of tissues in vitro, all the functional and morphological features must be recapitulated. To address this challenge, scaffold-free approaches have emerged as powerful strategies for the fabrication of tissue constructs with enhanced deposition of extracellular matrix, essential for the natural development of the tissue architecture. Nevertheless, the traditional approaches still fail on engineering tissues with high level of complexity, as seen in stratified and hierarchical conformations, as well with adequate mechanical performance. Therefore, this PhD proposal aimed to develop improved tissue substitutes that closely mimic key functional aspects of the native microenvironment. By using magnetized cells as basic living units, we propose the fabrication of magnetic membranes of cells through magnetic force-based tissue engineering (Mag-TE). The magnetic character of the created tissues allowed a precise control over cells’ positioning and, consequently, an extremely guided-assembling of the tissues. Following this strategy, cohesive and robust macrotissues with enhanced mechanical behavior were fabricated, circumventing one of the major limitations of scaffold-free approaches which includes the development of mechanically weak tissue constructs. Concerning the architecture of the native tissues, magnetic living substitutes with intricate geometries were developed, attesting the versatility of this approach. Another problematic regarding the development of tissue substitutes is the lack of adequate diffusion of nutrients and oxygen, which may lead to premature cell death. To overcome this obstacle, we engineered pre-vascularized multilayered cell sheets, exhibiting preserved human vascular structures and the ability to integrate the host vasculature. In this thesis, small tissue units at the microscale were also designed through the combination of Mag-TE and a high-throughput platform. These microtissues could further act as living building blocks for the fabrication of larger heterotypic tissue constructs or as in vitro platforms for disease modelling and drug screening. Finally, by exploring the magnetic character of our improved living tissues, we evaluated the role of magnetic field on modulating the cell fate of tissues produced in vitro. Upon magnetic stimulation, we triggered the osteogenic differentiation of the magnetized tissues, opening new possibilities for advanced strategies in bone regeneration. Using an in vivo mice model, we were also able to stimulate tissue integration and the osteogenic differentiation of the implant in situ. By using magnetized cells as building materials, we envisaged the fabrication of complex multiscale and multifunctional tissues with clinical relevance. The magnetic features of the designed tissues could accelerate the translation of Mag-TE to the clinical practices, allowing the remote and in situ guiding of implants into the expected tissue function, while guarantying a feasible monitoring and tracking along the time.O principal objetivo da engenharia de tecidos consiste no desenvolvimento de substitutos biológicos para reparar ou substituir tecidos danificados. No entanto, o fabrico de tecidos funcionais continua ilusório, dificultando a sua translação para a prática clínica. Durante o design de tecidos in vitro, todas as características funcionais e morfológicas devem ser recapituladas. Para resolver este desafio, a abordagem “scaffold-free” emergiu como uma estratégia poderosa no fabrico de tecidos, com uma deposição de matriz extracelular aprimorada, essencial para o desenvolvimento da arquitetura natural dos tecidos. No entanto, as abordagens tradicionais ainda falham na engenharia de tecidos com alto grau de complexidade, como visto em conformações estratificadas e hierárquicas, bem como com desempenho mecânico adequado. Assim, este projeto de doutoramento pretendeu desenvolver substitutos de tecidos aprimorados, mimetizando aspetos funcionais chave do microambiente nativo. Utilizando células magnetizadas como unidade base, propomos o fabrico de folhas de tecidos magnéticas por engenharia de tecidos baseada em força magnética. O caracter magnético permitiu o controlo preciso sobre o posicionamento das células e consequentemente, uma construção extremamente guiada dos tecidos. Seguindo essa estratégia, foram fabricados macrotecidos coesos e robustos com comportamento mecânico aprimorado, contornando uma das principais limitações da abordagem “scaffold-free”, que inclui o desenvolvimento de construções de tecidos mecanicamente fracos. Relativamente à arquitetura dos tecidos nativos, foram fabricados tecidos magnéticos com geometrias complexas, atestando a versatilidade desta abordagem. Outro problema é a inadequada difusão de nutrientes e oxigénio, levando à morte celular prematura. Para ultrapassar este obstáculo, projetamos folhas tecidulares em multicamada pré-vascularizadas, exibindo uma estrutura vascular humana preservada e a capacidade de integrar a vasculatura do hospedeiro. Nesta tese, pequenas unidades de tecidos à microescala foram também desenhadas através da combinação da engenharia de tecidos baseada em força magnética e uma plataforma de alto rendimento. Estes microtecidos podem atuar ainda como blocos de construção para a fabricação de construções de tecidos heterotípicos maiores ou como plataformas in vitro para screening de doenças e fármacos. Finalmente, explorando o caracter magnético dos nossos tecidos vivos aprimorados, avaliamos o papel do campo magnético na modulação do comportamento celular dos tecidos produzidos in vitro. Depois de estimulados magneticamente, a diferenciação osteogénica dos tecidos magnetizados foi incitada, abrindo novas possibilidades para estratégias avançadas na regeneração do osso. Utilizando um modelo vivo de ratinho, podemos estimular a integração do tecido e diferenciação osteogénica do implante. Usando células magnetizadas como unidades de construção, prevemos o fabrico de tecidos complexos e multifuncionais com relevância clínica. O caracter magnético dos tecidos poderá potenciar a translação, permitindo a orientação remota e local (in situ) do implante na função do tecido esperado, garantindo também uma adequada monitorização ao longo do tempo.2023-06-22T14:09:07Z2023-05-04T00:00:00Z2023-05-04doctoral thesisinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/10773/38207engSantos, Lúcia Isabel Ferreirainfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-06T04:46:27Zoai:ria.ua.pt:10773/38207Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T14:20:02.018793Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Magnetic responsive cell-based platforms for tissue engineering applications |
title |
Magnetic responsive cell-based platforms for tissue engineering applications |
spellingShingle |
Magnetic responsive cell-based platforms for tissue engineering applications Santos, Lúcia Isabel Ferreira Cell sheet Magnetic field Mechanotransduction Stem cells Tissue engineering |
title_short |
Magnetic responsive cell-based platforms for tissue engineering applications |
title_full |
Magnetic responsive cell-based platforms for tissue engineering applications |
title_fullStr |
Magnetic responsive cell-based platforms for tissue engineering applications |
title_full_unstemmed |
Magnetic responsive cell-based platforms for tissue engineering applications |
title_sort |
Magnetic responsive cell-based platforms for tissue engineering applications |
author |
Santos, Lúcia Isabel Ferreira |
author_facet |
Santos, Lúcia Isabel Ferreira |
author_role |
author |
dc.contributor.author.fl_str_mv |
Santos, Lúcia Isabel Ferreira |
dc.subject.por.fl_str_mv |
Cell sheet Magnetic field Mechanotransduction Stem cells Tissue engineering |
topic |
Cell sheet Magnetic field Mechanotransduction Stem cells Tissue engineering |
description |
The major goal of tissue engineering consists on the development of biological substitutes to repair or replace damaged tissues. However, the fabrication of clinically relevant tissue replacements is still illusory, hampering their transactional to clinical practices. During the design of tissues in vitro, all the functional and morphological features must be recapitulated. To address this challenge, scaffold-free approaches have emerged as powerful strategies for the fabrication of tissue constructs with enhanced deposition of extracellular matrix, essential for the natural development of the tissue architecture. Nevertheless, the traditional approaches still fail on engineering tissues with high level of complexity, as seen in stratified and hierarchical conformations, as well with adequate mechanical performance. Therefore, this PhD proposal aimed to develop improved tissue substitutes that closely mimic key functional aspects of the native microenvironment. By using magnetized cells as basic living units, we propose the fabrication of magnetic membranes of cells through magnetic force-based tissue engineering (Mag-TE). The magnetic character of the created tissues allowed a precise control over cells’ positioning and, consequently, an extremely guided-assembling of the tissues. Following this strategy, cohesive and robust macrotissues with enhanced mechanical behavior were fabricated, circumventing one of the major limitations of scaffold-free approaches which includes the development of mechanically weak tissue constructs. Concerning the architecture of the native tissues, magnetic living substitutes with intricate geometries were developed, attesting the versatility of this approach. Another problematic regarding the development of tissue substitutes is the lack of adequate diffusion of nutrients and oxygen, which may lead to premature cell death. To overcome this obstacle, we engineered pre-vascularized multilayered cell sheets, exhibiting preserved human vascular structures and the ability to integrate the host vasculature. In this thesis, small tissue units at the microscale were also designed through the combination of Mag-TE and a high-throughput platform. These microtissues could further act as living building blocks for the fabrication of larger heterotypic tissue constructs or as in vitro platforms for disease modelling and drug screening. Finally, by exploring the magnetic character of our improved living tissues, we evaluated the role of magnetic field on modulating the cell fate of tissues produced in vitro. Upon magnetic stimulation, we triggered the osteogenic differentiation of the magnetized tissues, opening new possibilities for advanced strategies in bone regeneration. Using an in vivo mice model, we were also able to stimulate tissue integration and the osteogenic differentiation of the implant in situ. By using magnetized cells as building materials, we envisaged the fabrication of complex multiscale and multifunctional tissues with clinical relevance. The magnetic features of the designed tissues could accelerate the translation of Mag-TE to the clinical practices, allowing the remote and in situ guiding of implants into the expected tissue function, while guarantying a feasible monitoring and tracking along the time. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-06-22T14:09:07Z 2023-05-04T00:00:00Z 2023-05-04 |
dc.type.driver.fl_str_mv |
doctoral thesis |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10773/38207 |
url |
http://hdl.handle.net/10773/38207 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia instacron:RCAAP |
instname_str |
FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
collection |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
repository.name.fl_str_mv |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
repository.mail.fl_str_mv |
info@rcaap.pt |
_version_ |
1833594504960016384 |