Department of Chemistry, Korea University, Seoul 136-701, Korea.
Mol Cells. 2011 Aug;32(2):113-21. doi: 10.1007/s10059-011-1024-4. Epub 2011 Mar 24.
The ethical issues and public concerns regarding the use of embryonic stem (ES) cells in human therapy have motivated considerable research into the generation of pluripotent stem cell lines from non-embryonic sources. Numerous reports have shown that pluripotent cells can be generated and derived from germline stem cells (GSCs) in mouse and human testes during in vitro cultivation. The gene expression patterns of these cells are similar to those of ES cells and show the typical self-renewal and differentiation patterns of pluripotent cells in vivo and in vitro. However, the mechanisms underlying the spontaneous dedifferentiation of GSCs remain to be elucidated. Studies to identify master regulators in this reprogramming process are of critical importance for understanding the gene regulatory networks that sustain the cellular status of these cells. The results of such studies would provide a theoretical background for the practical use of these cells in regenerative medicine. Such studies would also help elucidate the molecular mechanisms underlying certain diseases, such as testicular germ cell tumors.
胚胎干细胞(ES)在人类治疗中的应用所引发的伦理问题和公众关注,促使人们对从非胚胎来源生成多能干细胞系进行了大量研究。大量报道表明,在体外培养过程中,多能细胞可以从老鼠和人类睾丸的生殖干细胞(GSCs)中生成和衍生。这些细胞的基因表达模式与 ES 细胞相似,表现出多能细胞在体内和体外的典型自我更新和分化模式。然而,GSCs 自发去分化的机制仍有待阐明。鉴定该重编程过程中的主调控因子的研究对于理解维持这些细胞细胞状态的细胞基因调控网络至关重要。这些研究的结果将为这些细胞在再生医学中的实际应用提供理论基础。这些研究还有助于阐明某些疾病(如睾丸生殖细胞肿瘤)的分子机制。