Abstract
Cryopreservation of somatic tissue can be applied in biodiversity conservation, especially for wild species as collared peccary. We aimed to evaluate the effect of vitrification techniques of ear tissue of collared peccary [direct vitrification in cryovials (DVC) or solid-surface vitrification (SSV)] on the layers of epidermis and dermis by conventional histology and cell ability during the in vitro culture. Thus, both the vitrification methods were able to maintain normal patterns of the epidermis as the cornea and granular layers, furthermore the intercellular space and dermal–epidermal junction of the spinous layer when compared to fresh control. Nevertheless, DVC and SSV percentage of normality decreased in the morphological integrity of cytoplasm (37.5 and 25.0%) of spinous layer, respectively, as compared to the fresh fragments (100%, p < 0.05). Moreover, other differences between the fresh control (100%) and DVC tissues were verified in the intra-epidermal cleavage of the spinous (37.5%) and basal (37.5%) layers. In general, DVC and SSV techniques were efficient for the recovery of the somatic cells according to most of the evaluated parameters for the in vitro culture (p > 0.05). In addition, only at time of 72 h (D3), in the growth curve, DVC fragments showed a reduced cell concentration than fresh control. In conclusion, SSV was found to be a more efficient method for vitrifying collared peccary skin tissue when compared to DVC. These results are relevant for the tissue cryopreservation from collared peccary and could also be useful for mammals with phylogenetic relationships.
Similar content being viewed by others
References
Abazari A, Jomha NM, Elliott JA, McGann LE (2013) Cryopreservation of articular cartilage. Cryobiology 66:201–209. doi:10.1016/j.cryobiol.2013.03.001
Aerts JMJ, De Clercq JBP, Andries S, Leroy JLMR, Van Aelst S, Bols PEJ (2008) Follicle survival and growth to antral stages in short-term murine ovarian cortical transplants after Cryologic solid surface vitrification or slow-rate freezing. Cryobiology 57:163–169. doi:10.1016/j.cryobiol.2008.07.011
Al-Aghbari AM, Menino AR Jr (2002) Survival of oocytes recovered from vitrified sheep ovarian tissues. Anim Reprod Sci 71:101–110. doi:10.1016/S0378-4320(02)00011-8
Bos-Mikich A, Marques L, Rodrigues JL, Lothhammer N, Frantz N (2012) The use of a metal container for vitrification of mouse ovaries, as a clinical grade model for human ovarian tissue cryopreservation, after different times and temperatures of transport. J Assist Reprod Genet 29:1267–1271. doi:10.1007/s10815-012-9867-y
Brockbank KG, Chen ZZ, Song YC (2010) Vitrification of porcine articular cartilage. Cryobiology 60:217–221. doi:10.1016/j.cryobiol.2009.12.003
Caputcu AT, Akkoc T, Cetinkaya G, Arat S (2013) Tissue cryobanking for conservation programs: effect of tissue type and storage time after death. Cell Tissue Bank 14:1–10. doi:10.1007/s10561-012-9292-6
Carvalho AA, Faustino LR, Silva CMG, Castro SV, Luz HKM, Rossetto R, Lopes CAP, Figueiredo JR, Rodrigues APR, Costa APR (2011) Influence of vitrification techniques and solutions on themorphology and survival of preantral follicles after in vitro culture of caprine ovarian tissue. Theriogenology 76:933–941. doi:10.1016/j.theriogenology.2011.04.024
Carvalho AA, Faustino LR, Silva CMG, Castro SV, Lopes CAP, Santos RR, Báo SN, Figueiredo JR, Rodrigues APR (2013) Novel wide-capacity method for vitrification of caprine ovaries: ovarian tissue cryosystem (OTC). Anim Reprod Sci 138:220–227. doi:10.1016/j.anireprosci.2013.02.015
Cetinkaya G, Arat S (2011) Cryopreservation of cartilage cell and tissue for biobanking. Cryobiology 63:292–297. doi:10.1016/j.cryobiol.2013.11.008
Costa UM, Reischak D, Silva J, Ravassolo AP (2005) Establishment and partial characterization of an ovine synovial membrane cell line obtained by transformation with Simian vírus 40 T antigen. J Virol Methods 128:72–78. doi:10.1016/j.jviromet.2005.03.019
Dariolli R, Bassaneze V, Nakamuta JS, Omae SV, Campos LCG, Krieger JE (2013) Porcine adipose tissue-derived mesenchymal stem cells retain their proliferative characteristics, senescence, karyotype and plasticity after long-term cryopreservation. PLoS ONE 8:e67939. doi:10.1371/journal.pone.0067939
Debeer S, Le Luduec JB, Kaiserlian D, Laurent P, Nicolas JF, Dubois B, Kanitakis J (2013) Comparative histology and immunohistochemistry of porcine versus human skin. Eur J Dermatol 23:456–466. doi:10.1684/ejd.2013.2060
Desbiez ALJ, Keuroghlian A, Beisiegel BM, Medici EP, Gatti A, Pontes ARM, Campos CB, Tófoli CF, Moraes Junior EA, Azevedo FC, Pinho GM, Cordeiro JLP, Santos Junior TS, Morais AA, Mangini PR, Flesher K, Rodrigues LF, Almeida LB (2012) Avaliação do risco de extinção do cateto Pecari tajacu Linnaeus, 1758, no Brasil. Biod Bras 3:74–83
Folch J, Cocero MJ, Chesné P, Alabart JL, Domínguez V, Cognié Y, Vignon X (2009) First birth of an animal from an extinct subspecies (Capra pyrenaica pyrenaica) by cloning. Theriogenology 71:1026–1034. doi:10.1016/j.theriogenology.2008.11.005
Ge L, Sun L, Chen J, Mao X, Kong Y, Xiong F, Wu J, Wei H (2010) The viability change of pigskin in vitro. Burns 36:533–538. doi:10.1016/j.burns.2009.08.001
Guan WJ, Liu CQ, Li CY, Liu D, Zhang WX, Ma YH (2010) Establishment and cryopreservation of a fibroblast cell line derived from Bengal tiger (Panthera tigris tigris). Cryoletters 31:130–138
Hao Y, Wax D, Zhong Z, Murphy C, Ross JW, Rieke A, Sutovsky P (2009) Porcine skin-derived stem cells can serve as donor cells for nuclear transfer. Cloning Stem Cells 11:101–109. doi:10.1089/clo.2008.0063
Hu PF, Guan WJ, Li XC, Zhang WX, Li CL, Ma YH (2013) Study on characteristics of in vitro culture and intracellular transduction of exogenous proteins in fibroblast cell line of Liaoning cashmere goat. Mol Biol Rep 40:327–336. doi:10.1007/s11033-012-2064-3
IUCN (2016) IUCN Red List of Threatened Species. Version 2015.4. http://dx.doi.org/10.2305/IUCN.UK.2015-2.RLTS.T4015A72587993.en. www.iucnredlist.org. Accessed 13 Apr 2016
Jomha NM, Anoop PC, Bagnall K, Mcgann LE (2002) Effects of increasing concentrations of dimethyl sulfoxide during cryopreservation of porcine articular cartilage. Cell Preserv Technol 1:111–120. doi:10.1089/153834402320882610
León-Quinto T, Simon MA, Cadenas R, Jones J, Martinez-Hernandez FJ, Moreno JM, Soria B (2009) Developing biological resource banks as a supporting tool for wildlife reproduction and conservation: the Iberian lynx bank as a model for other endangered species. Anim Rep Sci 112:347–361. doi:10.1016/j.anireprosci.2008.05.070
León-Quinto T, Simón MA, Sánchez Á, Martín F, Soria B (2011) Cryobanking the genetic diversity in the critically endangered Iberian lynx (Lynx pardinus) from skin biopsies. Investigating the cryopreservation and culture ability of highly valuable explants and cells. Cryobiology 62:145–151. doi:10.1016/j.cryobiol.2011.02.001
León-Quinto T, Simón MA, Cadenas R, Martínez Á, Serna A (2014) Different cryopreservation requirements in foetal versus adult skin cells from an endangered mammal, the Iberian lynx (Lynx pardinus). Cryobiology 68:227–233. doi:10.1016/j.cryobiol.2014.02.001
Li XC, Yue H, Li CY, He XH, Zhao QJ, Ma YH, Ma JZ (2009) Establishment and characterization of a fibroblast cell line derived from jining black grey goat for genetic conservation. Small Rumin Res 87:17–26. doi:10.1016/j.smallrumres.2009.09.028
Magalhães R, Nugraha B, Pervaiz S, Yu H, Kuleshova LL (2012) Influence of cell culture configuration on the post-cryopreservation viability of primary rat hepatocytes. Biomaterials 33:829–836. doi:10.1016/j.biomaterials.2011.10.015
May S, Wainwright JF (1985) Optimum warming rates to maintain glucose metabolism in porcine skin cryopreserved by slow cooling. Cryobiology 22:196–202. doi:10.1016/0011-2240(85)90175-0
Mehrabani D, Manafi N (2013) Role of cultured skin fibroblasts in aesthetic and plastic surgery. World J Plast Surg 2:2–5
Mehrabani D, Mahboobi R, Dianatpour M, Zare S, Tamadon A, Hosseini SE (2014) Establishment, culture, and characterization of guinea pig fetal fibroblast cell. Vet Med Int 2014:1–5. doi:10.1155/2014/510328
Moniruzzaman M, Bao RM, Taketsuru H, Miyano T (2009) Development of vitrified porcine primordial follicles in xenografts. Theriogenology 72:280–288. doi:10.1016/j.theriogenology.2009.01.024
Nogueira SS, Nogueira-Filho SL (2011) Wildlife farming: an alternative to unsustainable hunting and deforestation in Neotropical forests? Biodivers Conserv 20:1385–1397. doi:10.1007/s10531-011-0047-7
Praus R, Böhm F, Dvořák R (1980) Skin cryopreservation: I. Incorporation of radioactive sulfate as a criterion of pigskin graft viability after freezing to −196 °C in the presence of cryoprotectants. Cryobiology 17:130–134. doi:10.1016/0011-2240(80)90017-6
Rodrigues JP, Paraguassu-Braga FH, Carvalho L, Abdelhay E, Bouzas LF, Porto LC (2008) Evaluation of trehalose and sucrose as cryoprotectants for hematopoietic stem cells of umbilical cord blood. Cryobiology 56:144–151. doi:10.1016/j.cryobiol.2008.01.003
Roth V (2006) http://www.doubling-time.com/compute.php. Accessed 14 May 2015
Saini M, Selokar NL, Raja AK, Sahare AA, Singla SK, Chauhan MS, Palta P (2015) Effect of donor cell type on developmental competence, quality, gene expression, and epigenetic status of interspecies cloned embryos produced using cells from wild buffalo and oocytes from domestic buffalo. Theriogenology 84:101–108. doi:10.1016/j.theriogenology.2015.02.018
Santos RR, Tharasanit T, Van Haeften T, Figueiredo JR, Silva JRV, Van den Hurk R (2007) Vitrification of goat preantral follicles enclosed in ovarian tissue by using conventional and solid-surface vitrification methods. Cell Tissue Res 327:167–176. doi:10.1007/s00441-006-0240-2
Santos DO, Mendes A, Nogueira SSDC, Nogueira Filho SLG (2009) Criação comercial de caititus (Pecari tajacu): uma alternativa para o agronegócio. Rev Bras Saúde Prod Anim 10:1–11
Saragusty J, Arav A (2011) Current progress in oocyte and embryo cryopreservation by slow freezing and vitrification. Reproduction 141:1–19. doi:10.1530/REP-10-0236
Shah SM, Saini N, Ashraf S, Singh MK, Manik RS, Singla SK, Palta P, Chauhan MS (2015) Bone morphogenetic protein 4 (BMP4) induces buffalo (Bubalus bubalis) embryonic stem cell differentiation into germ cells. Biochimie 119:113–124. doi:10.1016/j.biochi.2015.10.021
Silvestre MA, Saeed AM, Escriba MJ, García-Ximénez F (2002) Vitrification and rapid freezing of rabbit fetal tissues and skin samples from rabbits and pigs. Theriogenology 58:69–76. doi:10.1016/S0093-691X(02)00830-0
Silvestre MA, Saeed AM, Cervera RP, Escribá MJ, García-Ximénez F (2003) Rabbit and pig ear skin sample cryobanking: effects pf storage time and temperature of the whole ear extirpated immediately after death. Theriogenology 59:1469–1477. doi:10.1016/S0093-691X(02)01185-8
Silvestre MA, Sánchez JP, Gómez EA (2004) Vitrification of goat, sheep, and cattle skin samples from whole ear extirpated after death and maintained at different storage times and temperatures. Theriogenology 49:221–229. doi:10.1016/j.cryobiol.2004.08.001
Song J, Hua S, Song K, Zhang Y (2007) Culture, characteristics and chromosome complement of Siberian tiger fibroblasts for nuclear transfer. In Vitro Cell Dev Biol Anim 43:203–209. doi:10.1007/s11626-007
Strober W (2001) Trypan blue exclusion test of cell viability. Curr Protoc Immunol. doi:10.1002/0471142735.ima03bs21
Summerfield A, Meurens F, Ricklin ME (2015) The immunology of the porcine skin and its value as a model for human skin. Mol Immunol 66:14–21. doi:10.1016/j.burns.2012.02.008
Acknowledgements
This study was supported by Brazilian Council of Scientific Development–CNPq (Process No. 477710/2013-1). The authors thank the Centre for Wild Animals Multiplication (CEMAS/UFERSA) for providing the animals and the Laboratory Gonadal Transplantation and In Vitro Embryo Production (LTG-PIV/UFERSA) for technical assistance. AR Silva and MF Oliveira were recipients of CNPq Grants.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Borges, A.A., Lima, G.L., de Queiroz Neta, L.B. et al. Conservation of somatic tissue derived from collared peccaries (Pecari tajacu Linnaeus, 1758) using direct or solid-surface vitrification techniques. Cytotechnology 69, 643–654 (2017). https://doi.org/10.1007/s10616-017-0074-7
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10616-017-0074-7