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From the Cover: Testis tissue explantation cures spermatogenic failure in c-Kit ligand mutant mice

机译:从封面:睾丸组织移植治疗c-Kit配体突变小鼠的生精功能衰竭

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摘要

Male infertility is most commonly caused by spermatogenic defects or insufficiencies, the majority of which are as yet cureless. Recently, we succeeded in cultivating mouse testicular tissues for producing fertile sperm from spermatogonial stem cells. Here, we show that one of the most severe types of spermatogenic defect mutant can be treated by the culture method without any genetic manipulations. The Sl/Sld mouse is used as a model of such male infertility. The testis of the Sl/Sld mouse has only primitive spermatogonia as germ cells, lacking any sign of spermatogenesis owing to mutations of the c-kit ligand (KITL) gene that cause the loss of membrane-bound-type KITL from the surface of Sertoli cells. To compensate for the deficit, we cultured testis tissues of Sl/Sld mice with a medium containing recombinant KITL and found that it induced the differentiation of spermatogonia up to the end of meiosis. We further discovered that colony stimulating factor-1 (CSF-1) enhances the effect of KITL and promotes spermatogenesis up to the production of sperm. Microinsemination of haploid cells resulted in delivery of healthy offspring. This study demonstrated that spermatogenic impairments can be treated in vitro with the supplementation of certain factors or substances that are insufficient in the original testes.
机译:男性不育最常见的原因是生精缺陷或功能不全,其中大多数尚未治愈。最近,我们成功地培养了小鼠睾丸组织,以从精原干细胞中产生可育的精子。在这里,我们显示了最严重类型的生精缺陷突变体之一,无需任何遗传操作即可通过培养方法进行治疗。 Sl / Sl d 小鼠被用作这种男性不育症的模型。 Sl / Sl d 小鼠的睾丸仅具有原始的精原细胞作为生殖细胞,由于c-kit配体(KITL)基因的突变导致膜结合损失而缺乏任何精子发生的迹象。 Sertoli细胞表面的KITL型。为了弥补这一缺陷,我们用含有重组KITL的培养基培养了Sl / Sl d 小鼠的睾丸组织,发现其诱导了精原细胞的分化直至减数分裂的结束。我们进一步发现,集落刺激因子1(CSF-1)增强了KITL的作用,并促进了直至生精的精子发生。单倍体细胞的微授精导致健康的后代。这项研究表明,可以通过补充某些原睾丸中不足的因子或物质来体外治疗生精障碍。

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