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鱼类精原干细胞的生物学特性与鉴定

Biology and identity of fish spermatogonial stem cell.

作者信息

Lacerda Samyra Maria dos Santos Nassif, Costa Guilherme Mattos Jardim, de França Luiz Renato

机构信息

Laboratory of Cellular Biology, Department of Morphology, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais 31270-901, Brazil.

Laboratory of Cellular Biology, Department of Morphology, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais 31270-901, Brazil.

出版信息

Gen Comp Endocrinol. 2014 Oct 1;207:56-65. doi: 10.1016/j.ygcen.2014.06.018. Epub 2014 Jun 23.

Abstract

Although present at relatively low number in the testis, spermatogonial stem cells (SSCs) are crucial for the establishment and maintenance of spermatogenesis in eukaryotes and, until recently, those cells were investigated in fish using morphological criteria. The isolation and characterization of these cells in fish have been so far limited by the lack of specific molecular markers, hampering the high SSCs biotechnological potential for aquaculture. However, some highly conserved vertebrate molecular markers, such as Gfra1 and Pou5f1/Oct4, are now available representing important candidates for studies evaluating the regulation of SSCs in fish and even functional investigations using germ cells transplantation. A technique already used to demonstrate that, different from mammals, fish germ stem cells (spermatogonia and oogonia) present high sexual plasticity that is determined by the somatic microenvironment. As relatively well established in mammals, and demonstrated in zebrafish and dogfish, this somatic environment is very important for the preferential location and regulation of SSCs. Importantly, a long-term in vitro culture system for SSCs has been now established for some fish species. Therefore, besides the aforementioned possibilities, such culture system would allow the development of strategies to in vitro investigate key regulatory and functional aspects of germline stem cells (ex: self-renewal and/or differentiation) or to amplify SSCs of rare, endangered, or commercially valuable fish species, representing an important tool for transgenesis and the development of new biotechnologies in fish production.

摘要

精原干细胞(SSCs)在睾丸中的数量相对较少,但对于真核生物精子发生的建立和维持至关重要。直到最近,鱼类中的这些细胞都是根据形态学标准进行研究的。由于缺乏特异性分子标记,鱼类中这些细胞的分离和鉴定一直受到限制,这阻碍了SSCs在水产养殖中的巨大生物技术潜力。然而,现在有一些高度保守的脊椎动物分子标记,如Gfra1和Pou5f1/Oct4,它们是评估鱼类SSCs调控甚至利用生殖细胞移植进行功能研究的重要候选标记。一种已被用于证明与哺乳动物不同 的技术表明,鱼类生殖干细胞(精原细胞和卵原细胞)具有由体细胞微环境决定的高性可塑性。正如在哺乳动物中相对成熟,并在斑马鱼和角鲨中得到证明的那样,这种体细胞环境对于SSCs的优先定位和调控非常重要。重要的是,现在已经为一些鱼类建立了SSCs的长期体外培养系统。因此,除了上述可能性之外,这种培养系统将有助于开发策略,以体外研究生殖系干细胞的关键调控和功能方面(例如自我更新和/或分化),或扩增珍稀、濒危或具有商业价值鱼类的SSCs,这是鱼类生产中转基因和新生物技术发展的重要工具。

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