Cardoso Adauto Lima, Oliveira Jordana Inácio Nascimento, Climaco João Pedro Silva, Venturelli Natália Bortholazzi, do Nascimento Moreira Camila, Martins Cesar
Department of Structural and Functional Biology, Institute of Biosciences at Botucatu, São Paulo State University - UNESP, Botucatu, SP, 18618-689, Brazil.
In Vitro Cell Dev Biol Anim. 2024 Aug 8. doi: 10.1007/s11626-024-00963-7.
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.
辐鳍鱼纲(Actinopterygii)代表了最多样化的脊椎动物谱系,它们在生理、生活方式以及对海洋和淡水环境的适应方面表现出广泛的差异,并且有几种物种已被确立为生物学研究模型。细胞的体外培养是生物学研究多个领域的基础,是使用动物进行研究的一种替代方法。已经使用针对每种细胞类型和物种的特定方法建立了数百种鱼类细胞系。本文描述了一种可普遍用于从包括海洋和淡水物种在内的多种辐鳍鱼的尾鳍获取细胞培养物的方案。详细描述了样本采集、微生物消毒、组织解离、接种和培养、冷冻保存和解冻以及核型分析的条件。为归入12个不同目的20个物种建立了原代细胞培养物。其中11个物种是首次进行体外培养。起初,鱼类细胞培养物之间表现出不同的增殖能力;然而在传代过程中,大多数培养物开始具有相似的增殖速率。在整个传代过程中,注意到类似于成纤维细胞的细胞开始占主导地位。这些培养物的强大增殖能力揭示了它们成为细胞系的潜力。例如,墨西哥丽脂鲤(A. mexicanus)的培养物已经增殖了数月,并且已经传代到第65代。此外,与体内描述相比,这些细胞培养物显示出保守的二倍体染色体数,这表明这些培养物具有稳定的核型。因此,这些培养物有潜力用于毒理学、细胞遗传学、基因组学、病理学、免疫学、细胞农业和保护等多个领域,并且这种方法有潜力扩展到尚未测试的物种以及其他器官。