Revolutionizing disease modeling: the emergence of organoids in cellular systems

Detalhes bibliográficos
Autor(a) principal: Pedrosa, Ana Rita Silva
Data de Publicação: 2023
Outros Autores: Salgado, A. J., Ferreira, Pedro Eduardo Mendes
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/1822/83599
Resumo: Cellular models have created opportunities to explore the characteristics of human diseases through well-established protocols, while avoiding the ethical restrictions associated with post-mortem studies and the costs associated with researching animal models. The capability of cell reprogramming, such as induced pluripotent stem cells (iPSCs) technology, solved the complications associated with human embryonic stem cells (hESC) usage. Moreover, iPSCs made significant contributions for human medicine, such as in diagnosis, therapeutic and regenerative medicine. The two-dimensional (2D) models allowed for monolayer cellular culture in vitro; however, they were surpassed by the three-dimensional (3D) cell culture system. The 3D cell culture provides higher cell–cell contact and a multi-layered cell culture, which more closely respects cellular morphology and polarity. It is more tightly able to resemble conditions in vivo and a closer approach to the architecture of human tissues, such as human organoids. Organoids are 3D cellular structures that mimic the architecture and function of native tissues. They are generated in vitro from stem cells or differentiated cells, such as epithelial or neural cells, and are used to study organ development, disease modeling, and drug discovery. Organoids have become a powerful tool for understanding the cellular and molecular mechanisms underlying human physiology, providing new insights into the pathogenesis of cancer, metabolic diseases, and brain disorders. Although organoid technology is up-and-coming, it also has some limitations that require improvements.
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spelling Revolutionizing disease modeling: the emergence of organoids in cellular systemsCell cultureiPSCsDisease modelingOrganoidsOrganoids applicationsOrganoids limitationsScience & TechnologyCellular models have created opportunities to explore the characteristics of human diseases through well-established protocols, while avoiding the ethical restrictions associated with post-mortem studies and the costs associated with researching animal models. The capability of cell reprogramming, such as induced pluripotent stem cells (iPSCs) technology, solved the complications associated with human embryonic stem cells (hESC) usage. Moreover, iPSCs made significant contributions for human medicine, such as in diagnosis, therapeutic and regenerative medicine. The two-dimensional (2D) models allowed for monolayer cellular culture in vitro; however, they were surpassed by the three-dimensional (3D) cell culture system. The 3D cell culture provides higher cell–cell contact and a multi-layered cell culture, which more closely respects cellular morphology and polarity. It is more tightly able to resemble conditions in vivo and a closer approach to the architecture of human tissues, such as human organoids. Organoids are 3D cellular structures that mimic the architecture and function of native tissues. They are generated in vitro from stem cells or differentiated cells, such as epithelial or neural cells, and are used to study organ development, disease modeling, and drug discovery. Organoids have become a powerful tool for understanding the cellular and molecular mechanisms underlying human physiology, providing new insights into the pathogenesis of cancer, metabolic diseases, and brain disorders. Although organoid technology is up-and-coming, it also has some limitations that require improvements.This work was funded by national funds, through the Foundation for Science and Technology (FCT), a Ph.D. grant SFRH/BD/131540/2017, COVID/BD/152416/2022, UMINHO/BIMCNCG/2022/143, and project PTDC/SAU-PAR/2766/2021.info:eu-repo/semantics/publishedVersionMultidisciplinary Digital Publishing Institute (MDPI)Universidade do MinhoPedrosa, Ana Rita SilvaSalgado, A. J.Ferreira, Pedro Eduardo Mendes2023-03-1810000-01-01T00:00:00Z2023-03-18T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/83599engPedrosa, Ana; Salgado, António José; Ferreira, Pedro Eduardo, Revolutionizing disease modeling: the emergence of organoids in cellular systems. Cells, 12(6), 930, 20232073-440910.3390/cells1206093036980271930https://www.mdpi.com/journal/cellsinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:12:43Zoai:repositorium.sdum.uminho.pt:1822/83599Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:04:39.531381Repositório 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 Revolutionizing disease modeling: the emergence of organoids in cellular systems
title Revolutionizing disease modeling: the emergence of organoids in cellular systems
spellingShingle Revolutionizing disease modeling: the emergence of organoids in cellular systems
Pedrosa, Ana Rita Silva
Cell culture
iPSCs
Disease modeling
Organoids
Organoids applications
Organoids limitations
Science & Technology
title_short Revolutionizing disease modeling: the emergence of organoids in cellular systems
title_full Revolutionizing disease modeling: the emergence of organoids in cellular systems
title_fullStr Revolutionizing disease modeling: the emergence of organoids in cellular systems
title_full_unstemmed Revolutionizing disease modeling: the emergence of organoids in cellular systems
title_sort Revolutionizing disease modeling: the emergence of organoids in cellular systems
author Pedrosa, Ana Rita Silva
author_facet Pedrosa, Ana Rita Silva
Salgado, A. J.
Ferreira, Pedro Eduardo Mendes
author_role author
author2 Salgado, A. J.
Ferreira, Pedro Eduardo Mendes
author2_role author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Pedrosa, Ana Rita Silva
Salgado, A. J.
Ferreira, Pedro Eduardo Mendes
dc.subject.por.fl_str_mv Cell culture
iPSCs
Disease modeling
Organoids
Organoids applications
Organoids limitations
Science & Technology
topic Cell culture
iPSCs
Disease modeling
Organoids
Organoids applications
Organoids limitations
Science & Technology
description Cellular models have created opportunities to explore the characteristics of human diseases through well-established protocols, while avoiding the ethical restrictions associated with post-mortem studies and the costs associated with researching animal models. The capability of cell reprogramming, such as induced pluripotent stem cells (iPSCs) technology, solved the complications associated with human embryonic stem cells (hESC) usage. Moreover, iPSCs made significant contributions for human medicine, such as in diagnosis, therapeutic and regenerative medicine. The two-dimensional (2D) models allowed for monolayer cellular culture in vitro; however, they were surpassed by the three-dimensional (3D) cell culture system. The 3D cell culture provides higher cell–cell contact and a multi-layered cell culture, which more closely respects cellular morphology and polarity. It is more tightly able to resemble conditions in vivo and a closer approach to the architecture of human tissues, such as human organoids. Organoids are 3D cellular structures that mimic the architecture and function of native tissues. They are generated in vitro from stem cells or differentiated cells, such as epithelial or neural cells, and are used to study organ development, disease modeling, and drug discovery. Organoids have become a powerful tool for understanding the cellular and molecular mechanisms underlying human physiology, providing new insights into the pathogenesis of cancer, metabolic diseases, and brain disorders. Although organoid technology is up-and-coming, it also has some limitations that require improvements.
publishDate 2023
dc.date.none.fl_str_mv 10000-01-01T00:00:00Z
2023-03-18
2023-03-18T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://hdl.handle.net/1822/83599
url https://hdl.handle.net/1822/83599
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Pedrosa, Ana; Salgado, António José; Ferreira, Pedro Eduardo, Revolutionizing disease modeling: the emergence of organoids in cellular systems. Cells, 12(6), 930, 2023
2073-4409
10.3390/cells12060930
36980271
930
https://www.mdpi.com/journal/cells
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Multidisciplinary Digital Publishing Institute (MDPI)
publisher.none.fl_str_mv Multidisciplinary Digital Publishing Institute (MDPI)
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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