Genetic Strains Research Centre, National Institute of Genetics, Mishima 411-8540, Japan.
Genes Cells. 2012 Apr;17(4):316-25. doi: 10.1111/j.1365-2443.2012.01589.x. Epub 2012 Mar 5.
Germ-line stem cells have the potential to be a very powerful tool for modifying the genetic information of individual animals. As a first step to use spermatogonial stem cells (SSCs) to enable genetic modification, we here describe effective long-term culture conditions for propagating zebrafish SSCs and for the production of offspring from these cultured SSCs after their differentiation into sperm in transplanted testicular cell aggregates. Dissociated testicular cells were cultured in specific medium with some modified supplements, including several mammalian growth factors. The spermatogonia actively proliferated and retained the expression of exogenous green fluorescent protein under the control of vas and sox17 promoters and also of promyelocytic leukemia zinc finger (Plzf), a marker of undifferentiated spermatogonia, after 1 month in culture. This is a longer period than the entire natural spermatogenic cycle (from SSCs to sperm). The use of subcutaneously grafted aggregates of these cultured spermatogonia and freshly dissociated testicular cells showed that these SSCs could undergo self-renewal and differentiation into sperm. Artificial insemination of these grafted aggregates successfully produced offspring. This culture method will facilitate the identification of new factors for the maintenance of SSCs and enable the future enrichment of genetically modified SSCs that will produce offspring in zebrafish.
生殖干细胞有可能成为修改个体动物遗传信息的非常强大的工具。作为使用精原干细胞 (SSC) 实现基因修饰的第一步,我们在这里描述了有效且长期的培养条件,用于增殖斑马鱼 SSC,并在将这些培养的 SSC 分化为移植到睾丸细胞聚集体中的精子后产生后代。分离的睾丸细胞在含有一些改良补充剂的特定培养基中培养,包括几种哺乳动物生长因子。精原细胞在培养 1 个月后,在外源绿色荧光蛋白的控制下(受 vas 和 sox17 启动子的控制)以及未分化精原细胞的标志 promyelocytic leukemia zinc finger (Plzf) 的控制下,积极增殖并保留表达。这比整个自然精子发生周期(从 SSC 到精子)还要长。使用这些培养的精原细胞和新分离的睾丸细胞的皮下移植聚集体表明,这些 SSC 可以自我更新并分化为精子。对这些移植聚集体进行人工授精成功产生了后代。这种培养方法将有助于鉴定维持 SSC 的新因子,并能够富集未来产生后代的遗传修饰 SSC。