Investigating cryopreservation techniques for maintaining morphology and in vitro viability of cartilage and skin from Spix's yellow-toothed cavies (Galea spixii Wagler, 1831) for conservation through biobanks.

Autor: Olindo SL; Laboratory of Animal Biotechnology, Federal Rural University of Semiarid, Mossoro, 59625900, Brazil., de Aquino LVC; Laboratory of Animal Biotechnology, Federal Rural University of Semiarid, Mossoro, 59625900, Brazil., Moura YBF; Laboratory of Animal Biotechnology, Federal Rural University of Semiarid, Mossoro, 59625900, Brazil., E Silva YLF; Laboratory of Animal Biotechnology, Federal Rural University of Semiarid, Mossoro, 59625900, Brazil., Rodrigues ALR; Laboratory of Animal Biotechnology, Federal Rural University of Semiarid, Mossoro, 59625900, Brazil., da Silva VD; Laboratory of Animal Biotechnology, Federal Rural University of Semiarid, Mossoro, 59625900, Brazil., Pereira AF; Laboratory of Animal Biotechnology, Federal Rural University of Semiarid, Mossoro, 59625900, Brazil. alexsandra.pereira@ufersa.edu.br.
Jazyk: angličtina
Zdroj: Journal of molecular histology [J Mol Histol] 2024 Dec; Vol. 55 (6), pp. 1199-1209. Date of Electronic Publication: 2024 Sep 09.
DOI: 10.1007/s10735-024-10259-5
Abstrakt: Conservation of the genetic diversity through skin and cartilage biobanks represents an essential strategy for maintaining biodiversity. Biobanks for the wild species of the order Rodentia have been little studied. Considering that the cryopreservation technique has specific relationships with the tissue and species of interest, we propose investigating different techniques for preserving tissue integrity and cell viability after cartilage and skin culture from Spix's yellow-toothed cavies. Subsequently, two techniques [solid-surface vitrification (SSV) vs. slow freezing (SF)] were used for cartilage and skin cryopreservation. Tissues not subjected to cryopreservation were used as controls. All tissues were evaluated for morphology and proliferation by histological techniques. Moreover, fragments were cultured, and cells were evaluated for viability, proliferation, metabolism, and apoptosis. Regardless of the cryopreservation technique, no differences were observed for the thickness of the epidermis, dermis, skin, spinous and basal layers, fibroblasts, and proliferative activity regarding the number of nucleolar organizer regions (NOR). SSV ensured better maintenance of epidermal cells, normal chondrocytes, filled gaps, collagen fibers, proliferative activity by NOR area/cell, and reduced perinuclear halos and empty gaps compared to SF. SF ensured the conservation of corneum thickness compared to the control. Although both techniques promoted cell recovery after culture, cells from SF resulted in better subconfluence time and day with cell growth around fragments compared to SSV. In conclusion, both cryopreservation techniques resulted in viable cells after culture. However, SSV promoted better maintenance of tissue morphological integrity, and SF ensured the preservation of all cell quality parameters in Spix's yellow-toothed cavies.
Competing Interests: Declarations Competing interest The authors declare no Competing interest.
(© 2024. The Author(s), under exclusive licence to Springer Nature B.V.)
Databáze: MEDLINE
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