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Publicação:
Immunocytochemistry Analysis of HepG2 Cell 3D Culture Encapsulated as Spheroids in Alginate Beads

dc.contributor.authorMiranda, Raul Ghiraldelli
dc.contributor.authorFerraz, Elisa Raquel Anastácio
dc.contributor.authorPereira, Lilian Cristina [UNESP]
dc.contributor.authorDorta, Daniel Junqueira [UNESP]
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Federal Fluminense (UFF)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionBotucatu
dc.date.accessioned2021-06-25T10:50:04Z
dc.date.available2021-06-25T10:50:04Z
dc.date.issued2021-01-01
dc.description.abstract3D Cell culture is an alternative to animal use in many drug development and toxicity studies. The 3D cell culture can mimic and reproduce the original tissue microenvironment, morphology, and mechanical and physiological characteristics, to provide a more realistic and reliable response as compared to two-dimensional cultures. 3D cell culture encapsulated in alginate beads is a very simple and relatively inexpensive tool that is easy to handle and to maintain. The alginate beads function as a scaffold that imprisons cells and allows 3D cell growth, to generate spheroids that can have greater genic expression and cell–cell communication as a nano or microtissue. The HepG2 cell line is a human hepatocellular carcinoma cell derivative. HepG2 cells preserve several of the characteristics of hepatocytes and are therefore often used in toxicity studies. Here, we describe HepG2 cell encapsulation in alginate beads and analyze the resulting spheroids formed within the alginate beads by immunocytochemistry, by staining a certain structure with a specific antibody coupled with a fluorophore. This method preserves the beads and enables cell analysis by confocal microscopy.en
dc.description.affiliationDepartamento de Química Faculdade de Filosofia Ciências e Letras de Ribeirão Preto Universidade de São Paulo
dc.description.affiliationDepartment of Clinical Toxicological and Bromatological Analysis Faculty of Pharmaceutical Sciences of Ribeirão Preto University of São Paulo
dc.description.affiliationFaculdade de Farmácia Universidade Federal Fluminense
dc.description.affiliationDepartment of Bioprocesses and Biotechnology Faculty of Agronomic Sciences of Botucatu São Paulo State University
dc.description.affiliationCenter for Evaluation of Environmental Impact on Human Health (TOXICAM) Botucatu
dc.description.affiliationFFCLRP-USP Department of Chemistry Faculty of Philosophy Sciences and Letters of Ribeirão Preto University of São Paulo Ribeirão Preto
dc.description.affiliationInstituto Nacional de Tecnologias Alternativas de Detecção Avaliação Toxicologicae Remoção de Micropututantes e Radioativos (INCT-DATREM) Unesp Instituto de Química
dc.description.affiliationUnespDepartment of Bioprocesses and Biotechnology Faculty of Agronomic Sciences of Botucatu São Paulo State University
dc.description.affiliationUnespInstituto Nacional de Tecnologias Alternativas de Detecção Avaliação Toxicologicae Remoção de Micropututantes e Radioativos (INCT-DATREM) Unesp Instituto de Química
dc.format.extent197-206
dc.identifierhttp://dx.doi.org/10.1007/978-1-0716-1091-6_14
dc.identifier.citationMethods in Molecular Biology, v. 2240, p. 197-206.
dc.identifier.doi10.1007/978-1-0716-1091-6_14
dc.identifier.issn1940-6029
dc.identifier.issn1064-3745
dc.identifier.scopus2-s2.0-85099708839
dc.identifier.urihttp://hdl.handle.net/11449/207167
dc.language.isoeng
dc.relation.ispartofMethods in Molecular Biology
dc.sourceScopus
dc.subject3D culture
dc.subjectAlginate beads
dc.subjectConfocal microscopy
dc.subjectEncapsulation
dc.subjectHepG2
dc.subjectImmunocytochemistry
dc.titleImmunocytochemistry Analysis of HepG2 Cell 3D Culture Encapsulated as Spheroids in Alginate Beadsen
dc.typeCapítulo de livro
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentBioquímica e Tecnologia - IQpt

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