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超声引导下在山羊体内移植富集并冷冻保存的精原细胞悬液

Ultrasound guided transplantation of enriched and cryopreserved spermatogonial cell suspension in goats.

作者信息

Kaul G, Kaur J, Rafeeqi T A

机构信息

S.B. Laboratory-I, Animal Biochemistry Division, National Dairy Research Institute, (I.C.A.R.) Karnal-132001, Haryana, India.

出版信息

Reprod Domest Anim. 2010 Dec;45(6):e249-54. doi: 10.1111/j.1439-0531.2009.01549.x.

Abstract

Spermatogonial stem cells transplantation provides a unique approach for studying spermatogenesis. Initially developed in mice, this technique has now been extended in farm animals and provides an alternative means to preserve valuable male germ line and to produce transgenic animals. The aim of this study was to enrich type A spermatogonial cells amongst the isolated cells from goat testis, to cryopreserve these enriched populations of cells and their subsequent transplantation in unrelated recipient goats under ultrasound guidance. The cells were isolated enzymatically and enriched by differential plating and separation on discontinuous percoll gradient. Ultrasound guided injection of trypan blue dye into rete testis resulted in 20-30% filling of the seminiferous tubules. Prior to transplantation, the cells were labelled with a fluorescent dye to trace donor cells in recipient seminiferous tubules after transplantation. The fluorescent-labelled cells were observed up to 12 weeks after transplantation.

摘要

精原干细胞移植为研究精子发生提供了一种独特的方法。该技术最初在小鼠中开发,现已扩展到家畜中,并为保存有价值的雄性生殖系和生产转基因动物提供了一种替代手段。本研究的目的是从山羊睾丸分离的细胞中富集A型精原细胞,冷冻保存这些富集的细胞群体,并在超声引导下将其移植到无关的受体山羊体内。通过酶法分离细胞,并通过差异铺板和在不连续的Percoll梯度上分离进行富集。超声引导下将台盼蓝染料注入睾丸网导致20%-30%的生精小管被填充。在移植前,用荧光染料标记细胞,以便在移植后追踪受体生精小管中的供体细胞。移植后长达12周都能观察到荧光标记的细胞。

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