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Conditions for establishing fin primary cell cultures in a wide range of ray-finned fishes

dc.contributor.authorCardoso, Adauto Lima [UNESP]
dc.contributor.authorOliveira, Jordana Inácio Nascimento [UNESP]
dc.contributor.authorClimaco, João Pedro Silva [UNESP]
dc.contributor.authorVenturelli, Natália Bortholazzi [UNESP]
dc.contributor.authordo Nascimento Moreira, Camila [UNESP]
dc.contributor.authorMartins, Cesar [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T18:43:37Z
dc.date.issued2024-01-01
dc.description.abstractRay-finned fishes (Actinopterygii) represent the most diverse vertebrate lineage that show extensive variations in physiology, ways of life, and adaptations to marine and freshwater environments, and several species have been established as biological research models. The in vitro culture of cells is fundamental for several fields of biological research, being an alternative for studies that use animals. Hundreds of fish cell lines have been established using specific methods for each cell type and species. Here is described a protocol which can be used commonly for obtaining cell cultures from the caudal fin of a wide range of ray-finned fishes including marine and freshwater species. Conditions for sample collection, microbial disinfection, tissue dissociation, plating and incubation, cryopreservation and thawing, and karyotyping are described in detail. Primary cell cultures were developed for 20 species grouped into 12 different orders. Eleven of these species have been cultivated in vitro for the first time. In the beginning, the fish cell cultures showed different capacities of proliferation among them; however throughout the passages, most cultures began to have a similar proliferation rate. Throughout the passages, it was noticed that cells similar to fibroblasts began to predominate. The great proliferative ability of these cultures reveals their potential to become cell lines. The culture of A. mexicanus, for example, has been proliferating for months and is already in its 65th passage. Moreover, these cell cultures showed conserved diploid chromosome numbers in comparison with in vivo descriptions which suggest these cultures have stable karyotypes. Therefore, these cultures have potential to be used in several fields, such as toxicology, cytogenetics, genomics, pathology, immunology, cellular agriculture, and conservation, and this method has the potential to be expanded to species not yet tested, as well as to other organs.en
dc.description.affiliationDepartment of Structural and Functional Biology Institute of Biosciences at Botucatu São Paulo State University – UNESP, SP
dc.description.affiliationUnespDepartment of Structural and Functional Biology Institute of Biosciences at Botucatu São Paulo State University – UNESP, SP
dc.identifierhttp://dx.doi.org/10.1007/s11626-024-00963-7
dc.identifier.citationIn Vitro Cellular and Developmental Biology - Animal.
dc.identifier.doi10.1007/s11626-024-00963-7
dc.identifier.issn1543-706X
dc.identifier.issn1071-2690
dc.identifier.scopus2-s2.0-85200838293
dc.identifier.urihttps://hdl.handle.net/11449/299845
dc.language.isoeng
dc.relation.ispartofIn Vitro Cellular and Developmental Biology - Animal
dc.sourceScopus
dc.subjectActinopterygii
dc.subjectBiotechnology
dc.subjectConservation
dc.subjectCryopreservation
dc.subjectFins
dc.subjectInvitromatics
dc.titleConditions for establishing fin primary cell cultures in a wide range of ray-finned fishesen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationab63624f-c491-4ac7-bd2c-767f17ac838d
relation.isOrgUnitOfPublication.latestForDiscoveryab63624f-c491-4ac7-bd2c-767f17ac838d
unesp.author.orcid0000-0002-7287-5039[1]
unesp.author.orcid0000-0003-2511-1746[2]
unesp.author.orcid0000-0001-6894-409X[3]
unesp.author.orcid0000-0002-0287-6116[4]
unesp.author.orcid0000-0001-9490-5457[5]
unesp.author.orcid0000-0003-3534-974X[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt

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