Evidence map›Paper›PMID 39115629›Full record

ArticleIn vitro cellular & developmental biology. Animal2025

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

Adauto Lima Cardoso, Jordana Inácio Nascimento Oliveira, João Pedro Silva Climaco, Natália Bortholazzi Venturelli, Camila do Nascimento Moreira, Cesar Martins

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Article in In vitro cellular & developmental biology. Animal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Improve your success with fish cell lines-small things that matter.In vitro cellular & developmental biology. Animal · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Adauto Lima CardosoDepartment of Structural and Functional Biology, Institute of Biosciences at Botucatu, São Paulo State University - UNESP, Botucatu, SP, 18618-689, Brazil. adautolimacardoso@gmail.com.ORCID http://orcid.org/0000-0002-7287-5039
Jordana Inácio Nascimento OliveiraDepartment of Structural and Functional Biology, Institute of Biosciences at Botucatu, São Paulo State University - UNESP, Botucatu, SP, 18618-689, Brazil.ORCID http://orcid.org/0000-0003-2511-1746
João Pedro Silva ClimacoDepartment of Structural and Functional Biology, Institute of Biosciences at Botucatu, São Paulo State University - UNESP, Botucatu, SP, 18618-689, Brazil.ORCID http://orcid.org/0000-0001-6894-409X
Natália Bortholazzi VenturelliDepartment of Structural and Functional Biology, Institute of Biosciences at Botucatu, São Paulo State University - UNESP, Botucatu, SP, 18618-689, Brazil.ORCID http://orcid.org/0000-0002-0287-6116
Camila do Nascimento MoreiraDepartment of Structural and Functional Biology, Institute of Biosciences at Botucatu, São Paulo State University - UNESP, Botucatu, SP, 18618-689, Brazil.ORCID http://orcid.org/0000-0001-9490-5457
Cesar MartinsDepartment of Structural and Functional Biology, Institute of Biosciences at Botucatu, São Paulo State University - UNESP, Botucatu, SP, 18618-689, Brazil.ORCID http://orcid.org/0000-0003-3534-974X

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/16661-1Fundação de Amparo à Pesquisa do Estado de São Paulo 2017/07484-4Fundação de Amparo à Pesquisa do Estado de São Paulo 2017/25193-7Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/09553-6Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/25350-8Fundação de Amparo à Pesquisa do Estado de São Paulo 2022/02544-7
6 · The paper itself

Abstract

Ray-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.

Indexed as

Animal FinsCell Culture TechniquesFishesPrimary Cell CultureAnimalsCell ProliferationCryopreservationKaryotypingActinopterygiiBiotechnologyConservationCryopreservationFinsInvitromatics

Identifiers

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.