Obtaining a culture of somatic cells using tissue material from the ear of dead sheep/snow sheep hybrid

E. Shedova, E. Tsyndrina
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Abstract

Production and cryopreservation of somatic cells (SCs) from valuable and endangered animals allows a preservation of genetic diversity and ensuring their future reproduction. The aim of present work was to isolate SCs from the ear of unique hybrid sheep (Ovis aries) and snow sheep (Ovis nivicola borealis) post-mortem. In this purpose, enzymatic and mechanical methods of tissue preparation were compared.Materials and Methods. Ears from deceased animal were brought to the laboratory 12 hours after the death in a pasture, and biological material was thoroughly washed under running water. The hairs were removed from the part of the ear shell by the blade. Skin fragments were treated with 70% ethyl alcohol, washed three times in a saline solution with antibiotics and ground up to small pieces. The ear pieces were washed several times in phosphate buffer saline and divided into two parts. One part of the explants started in vitro culture without enzymatic treatment (group 1), whereas another part was pre-treated with a 0.25% trypsin/EDTA solution. After trypsinization, either tissue fragments (group 2), or cell complexes separated from cell suspension fraction (group 3) were taken for in vitro culture for 9 days. Monitoring of cell colony formation and growth was carried out daily. Results. In the group 3, cell colonies were formed on the second day of in vitro culture. In groups 1 and 2, cell growth was observed from tissue fragments after five days regardless of the treatment. On the 9th day, all the groups produced the primary cultures, represented by two types of SCs. In general, single cell complexes from the group 3 formed cell growth zones more quickly than tissue explants from the groups 1 and 2, however, final cultures of SCs and their morphological aspects were no different between the groups. Conclusion. Methodological protocols were proposed and successfully used to obtain in vitro cultures of SCs from the ear of dead sheep/snow sheep hybrid animal, 12 hours post-mortem that may allow further storage of valuable genetic material.
利用绵羊/雪羊杂种羊耳朵上的组织材料获得体细胞培养物
从珍贵和濒危动物身上提取体细胞(SCs)并将其冷冻保存,可以保护遗传多样性并确保其未来的繁殖。本研究的目的是从独特的杂交绵羊(Ovis aries)和雪山羊(Ovis nivicola borealis)死后的耳朵中分离体细胞。为此,比较了酶法和机械法制备组织的方法。动物死亡 12 小时后,将其耳朵带到实验室,在流水下彻底清洗生物材料。用刀片去除耳壳部分的毛发。皮肤碎片用 70% 的乙醇处理,在含抗生素的生理盐水中清洗三次,然后磨成小块。耳片在磷酸盐缓冲盐水中清洗数次,然后分成两部分。一部分外植体未经酶处理就开始体外培养(第 1 组),另一部分则用 0.25% 的胰蛋白酶/EDTA 溶液进行预处理。胰蛋白酶处理后,取组织碎片(第 2 组)或从细胞悬浮液中分离出的细胞复合物(第 3 组)进行体外培养,为期 9 天。每天监测细胞集落的形成和生长情况。结果第 3 组在体外培养的第二天就形成了细胞集落。在第 1 组和第 2 组中,无论处理方法如何,5 天后都能从组织碎片中观察到细胞生长。第 9 天,所有组都产生了初级培养物,由两种类型的 SCs 代表。一般来说,第 3 组的单细胞复合体比第 1 组和第 2 组的组织外植体更快形成细胞生长区,但各组的 SCs 最终培养物及其形态方面没有差异。结论本研究提出并成功使用了从死亡绵羊/雪羊杂交动物耳部获得 SCs 体外培养物的方法规程,该培养物可在死后 12 小时进一步储存有价值的遗传物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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