Safeguarding genetic resources of curassow through cryopreservation and transplantation of post-mortem recovered testicular cells into recipient roosters

Marcel Henrique Blank , Marcelo Demarchi Goissis , Roberto Motta de Avelar Azeredo , Luís Fábio Silveira , Ricardo José Garcia Pereira
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Abstract

Cryopreservation and transplantation of testicular cells (TCs), especially spematogonial stem cells (SSCs), offers a new perspective for the genetic rescue of birds since traditional biobanking using semen and eggs are either inefficient or impractical. Here, we demonstrated that transplantation of TCs (which contained SSCs) from dead curassows were able to survive and colonize chicken testes, despite the phylogenetic distance between donors and recipients. Previously to transplants, TCs were collected, cryopreserved, thawed, and then labelled with PKH26. Subsequently, labelled TCs were transferred into gonads of sterilized recipient chickens, and monitored for their presence and development from 1 to 180 days after transplantation. The interval between collecting testes and processing them in the laboratory was crucial for TCs viability, but it did not affect the viability of undifferentiated spermatogonia within 24 hours post-mortem. Although positive correlation between testis weight and the total cells recovered was noticed, the number of undifferentiated spermatogonia comprised approximately 0.05% of the total TCs. Once the number of undifferentiated spermagonial stem cells was not sufficient, we decided to make transplants using crude TC fractions containing different types of germ and somatic cells. PKH26-positive cells were found in the cryosections of recipient testes until 42 days after transplantation, whereas the presence of the donor genomic DNA was confirmed until 120 days after transplantation. Taken together, our findings indicate that chicken testes can provide functional conditions for the survival and proliferation of germ cells rescued from individuals of another family of the Galliformes order. This approach represents a promising conservation tool for the recovery of testicular germ cells (including SSCs) from individuals of different ages (from embryos to adult males).

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通过冷冻保存死后回收的睾丸细胞并将其移植到受体公鸡体内,保护水牛的遗传资源
睾丸细胞(TCs),尤其是睾丸干细胞(SSCs)的冷冻保存和移植为鸟类的基因拯救提供了一个新的视角,因为传统的精液和卵子生物库要么效率低下,要么不切实际。在这里,我们证明,尽管捐赠者和接受者之间存在系统发育上的距离,但从死亡的卷尾猴身上移植的TC(含有SSCs)能够存活并定植于鸡的睾丸。在移植前,先采集、低温保存、解冻 TC,然后用 PKH26 标记。随后,将标记的 TC 移植到已消毒的受体鸡的性腺中,并在移植后 1 到 180 天内监测其存在和发育情况。从采集睾丸到实验室处理睾丸之间的间隔时间对TC的存活率至关重要,但这并不影响死后24小时内未分化精原细胞的存活率。虽然睾丸重量与回收的细胞总数呈正相关,但未分化精原细胞的数量约占TC总数的0.05%。一旦未分化精原干细胞的数量不足,我们就决定使用含有不同类型生殖细胞和体细胞的粗TC碎片进行移植。直到移植后42天,我们才在受体睾丸的冷冻切片中发现PKH26阳性细胞,而直到移植后120天,我们才确认供体基因组DNA的存在。总之,我们的研究结果表明,鸡睾丸可以为从胆形目另一科个体中拯救的生殖细胞的存活和增殖提供功能条件。这种方法对于从不同年龄的个体(从胚胎到成年雄性个体)恢复睾丸生殖细胞(包括自体细胞)是一种很有前景的保护工具。
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来源期刊
Theriogenology wild
Theriogenology wild Animal Science and Zoology, Veterinary Science
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56 days
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