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

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 t...

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Veröffentlicht in:Journal of molecular histology 2024-12, Vol.55 (6), p.1199-1209
Hauptverfasser: Olindo, Samara Lima, de Aquino, Leonardo Vitorino Costa, Moura, Yasmin Beatriz França, e Silva, Yara Letícia Frutuoso, Rodrigues, Ana Lívia Rocha, da Silva, Vinicius Dantas, Pereira, Alexsandra Fernandes
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container_end_page 1209
container_issue 6
container_start_page 1199
container_title Journal of molecular histology
container_volume 55
creator Olindo, Samara Lima
de Aquino, Leonardo Vitorino Costa
Moura, Yasmin Beatriz França
e Silva, Yara Letícia Frutuoso
Rodrigues, Ana Lívia Rocha
da Silva, Vinicius Dantas
Pereira, Alexsandra Fernandes
description 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.
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subjects Animals
Apoptosis
Biobanks
Biodiversity
Biological Specimen Banks
Biomedical and Life Sciences
Biomedicine
Cartilage
Cartilage - cytology
Cell Biology
Cell culture
Cell Proliferation
Cell Survival
Cell viability
Chondrocytes
Conservation
Cryopreservation
Cryopreservation - methods
Dermis
Developmental Biology
Epidermis
Freezing
Genetic diversity
Life Sciences
Morphology
Nucleoli
Original Paper
Skin
Skin - cytology
Tissue culture
Vitrification
title 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
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