Samara Lima Olindo, Leonardo Vitorino Costa de Aquino, Yasmin Beatriz França Moura, Yara Letícia Frutuoso E Silva, Ana Lívia Rocha Rodrigues, Vinicius Dantas da Silva, Alexsandra Fernandes Pereira
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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. 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引用次数: 0
摘要
通过皮肤和软骨生物库保护遗传多样性是维护生物多样性的一项重要战略。对啮齿目野生物种生物库的研究很少。考虑到低温保存技术与所关注的组织和物种有特定的关系,我们建议研究不同的技术,以保存斯皮克斯黄齿狸软骨和皮肤培养后的组织完整性和细胞活力。随后,两种技术[固体表面玻璃化(SSV)与缓慢冷冻(SF)]被用于软骨和皮肤的冷冻保存。未进行冷冻保存的组织被用作对照组。所有组织均通过组织学技术进行形态和增殖评估。此外,还对碎片进行了培养,并对细胞的活力、增殖、新陈代谢和凋亡进行了评估。无论采用哪种冷冻保存技术,表皮、真皮、皮肤、棘层和基底层、成纤维细胞的厚度以及核组织区(NOR)数量方面的增殖活性均无差异。与 SF 相比,SSV 能更好地保持表皮细胞、正常软骨细胞、填充间隙、胶原纤维、NOR 面积/细胞的增殖活性,并减少核周晕和空隙。与对照组相比,SF 确保了角质层厚度的保持。虽然两种技术都能促进细胞培养后的恢复,但与 SSV 相比,SF 细胞的亚融合时间和细胞在碎片周围生长的天数更长。总之,两种冷冻保存技术都能使培养后的细胞存活。不过,SSV能更好地保持组织形态的完整性,而SF则能确保斯皮克斯黄牙豚所有细胞质量参数的保存。
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 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.
期刊介绍:
The Journal of Molecular Histology publishes results of original research on the localization and expression of molecules in animal cells, tissues and organs. Coverage includes studies describing novel cellular or ultrastructural distributions of molecules which provide insight into biochemical or physiological function, development, histologic structure and disease processes.
Major research themes of particular interest include:
- Cell-Cell and Cell-Matrix Interactions;
- Connective Tissues;
- Development and Disease;
- Neuroscience.
Please note that the Journal of Molecular Histology does not consider manuscripts dealing with the application of immunological or other probes on non-standard laboratory animal models unless the results are clearly of significant and general biological importance.
The Journal of Molecular Histology publishes full-length original research papers, review articles, short communications and letters to the editors. All manuscripts are typically reviewed by two independent referees. The Journal of Molecular Histology is a continuation of The Histochemical Journal.