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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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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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.</description><identifier>ISSN: 1567-2379</identifier><identifier>ISSN: 1567-2387</identifier><identifier>EISSN: 1567-2387</identifier><identifier>DOI: 10.1007/s10735-024-10259-5</identifier><identifier>PMID: 39249549</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>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</subject><ispartof>Journal of molecular histology, 2024-12, Vol.55 (6), p.1199-1209</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2024. 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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.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Biobanks</subject><subject>Biodiversity</subject><subject>Biological Specimen Banks</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cartilage</subject><subject>Cartilage - cytology</subject><subject>Cell Biology</subject><subject>Cell culture</subject><subject>Cell Proliferation</subject><subject>Cell Survival</subject><subject>Cell viability</subject><subject>Chondrocytes</subject><subject>Conservation</subject><subject>Cryopreservation</subject><subject>Cryopreservation - methods</subject><subject>Dermis</subject><subject>Developmental Biology</subject><subject>Epidermis</subject><subject>Freezing</subject><subject>Genetic diversity</subject><subject>Life Sciences</subject><subject>Morphology</subject><subject>Nucleoli</subject><subject>Original Paper</subject><subject>Skin</subject><subject>Skin - cytology</subject><subject>Tissue culture</subject><subject>Vitrification</subject><issn>1567-2379</issn><issn>1567-2387</issn><issn>1567-2387</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcGO1SAUhhujccbRF3BhSNyMiVUo0MLSTHScZBIXalw2FGjLTMu5Ar3ana_hc_kGPonce8fRuHABnMB3_nM4f1E8JvgFwbh5GQluKC9xxUqCKy5Lfqc4JrxuyoqK5u5t3Mij4kGMVxhXombyfnFEZcUkZ_K4-HHhtzYmN6jk_IB0WGETbLRhmy_Ao2T16N3nxUbUQ0Czcj7ltWNnCJsRJhhWpLxBzqOtSwHyrjo3ubQi6JFWIblJDXbPxOtM9QFm9H7jvv789j2i1U4TfCkTQBqtyfzW5Vqn52qyCsVMOYc-qWGy4TkigpJn-z40-L96HAMsw4g6B53y1_Fhca9XU7SPbs6T4uOb1x_O3paX784vzl5dlrridSqFIQILUwupRB4HVpUlwmgimaBMa4yZbCTG2Nje0E7K3tLGCNxhxXrGTU9PitOD7ibAbkKpnV3U-T_KW1hiS7MruGGCk4w-_Qe9giX43F2mKiEEr2uaqepA6QAxBtu3m-BmFdaW4HZneXuwvM2Wt3vLW56TntxIL91szW3Kb48zQA9AzE9-sOFP7f_I_gKSSbyC</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Olindo, Samara Lima</creator><creator>de Aquino, Leonardo Vitorino Costa</creator><creator>Moura, Yasmin Beatriz França</creator><creator>e Silva, Yara Letícia Frutuoso</creator><creator>Rodrigues, Ana Lívia Rocha</creator><creator>da Silva, Vinicius Dantas</creator><creator>Pereira, Alexsandra Fernandes</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20241201</creationdate><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</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c256t-8d1808d689a82490a2e18dc194834cc004979000defd3b99fe37d80b0a4f45df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Biobanks</topic><topic>Biodiversity</topic><topic>Biological Specimen Banks</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cartilage</topic><topic>Cartilage - cytology</topic><topic>Cell Biology</topic><topic>Cell culture</topic><topic>Cell Proliferation</topic><topic>Cell Survival</topic><topic>Cell viability</topic><topic>Chondrocytes</topic><topic>Conservation</topic><topic>Cryopreservation</topic><topic>Cryopreservation - methods</topic><topic>Dermis</topic><topic>Developmental Biology</topic><topic>Epidermis</topic><topic>Freezing</topic><topic>Genetic diversity</topic><topic>Life Sciences</topic><topic>Morphology</topic><topic>Nucleoli</topic><topic>Original Paper</topic><topic>Skin</topic><topic>Skin - cytology</topic><topic>Tissue culture</topic><topic>Vitrification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Olindo, Samara Lima</creatorcontrib><creatorcontrib>de Aquino, Leonardo Vitorino Costa</creatorcontrib><creatorcontrib>Moura, Yasmin Beatriz França</creatorcontrib><creatorcontrib>e Silva, Yara Letícia Frutuoso</creatorcontrib><creatorcontrib>Rodrigues, Ana Lívia Rocha</creatorcontrib><creatorcontrib>da Silva, Vinicius Dantas</creatorcontrib><creatorcontrib>Pereira, Alexsandra Fernandes</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of molecular histology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Olindo, Samara Lima</au><au>de Aquino, Leonardo Vitorino Costa</au><au>Moura, Yasmin Beatriz França</au><au>e Silva, Yara Letícia Frutuoso</au><au>Rodrigues, Ana Lívia Rocha</au><au>da Silva, Vinicius Dantas</au><au>Pereira, Alexsandra Fernandes</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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</atitle><jtitle>Journal of molecular histology</jtitle><stitle>J Mol Histol</stitle><addtitle>J Mol Histol</addtitle><date>2024-12-01</date><risdate>2024</risdate><volume>55</volume><issue>6</issue><spage>1199</spage><epage>1209</epage><pages>1199-1209</pages><issn>1567-2379</issn><issn>1567-2387</issn><eissn>1567-2387</eissn><abstract>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.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>39249549</pmid><doi>10.1007/s10735-024-10259-5</doi><tpages>11</tpages></addata></record> |
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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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