Siegel Nicol, Rosner Margit, Hanneder Michaela, Valli Alessandro, Hengstschläger Markus
Medical Genetics, Obstetrics and Gynecology, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.
Stem Cell Rev. 2007 Dec;3(4):256-64. doi: 10.1007/s12015-007-9003-z.
In future, the characterization and isolation of different human stem cells will allow the detailed molecular investigation of cell differentiation processes and the establishment of new therapeutic concepts for a wide variety of diseases. Since the first successful isolation and cultivation of human embryonic stem cells about 10 years ago, their usage for research and therapy has been constrained by complex ethical consideration as well as by the risk of malignant development of undifferentiated embryonic stem cells after transplantation into the patient's body. Adult stem cells are ethically acceptable and harbor a low risk of tumor development. However, their differentiation potential and their proliferative capacity are limited. About 4 years ago, the discovery of amniotic fluid stem cells, expressing Oct-4, a specific marker of pluripotent stem cells, and harboring a high proliferative capacity and multilineage differentiation potential, initiated a new and promising stem cell research field. In between, amniotic fluid stem cells have been demonstrated to harbor the potential to differentiate into cells of all three embryonic germlayers. These stem cells do not form tumors in vivo and do not raise the ethical concerns associated with human embryonic stem cells. Further investigations will reveal whether amniotic fluid stem cells really represent an intermediate cell type with advantages over both, adult stem cells and embryonic stem cells. The approach to generate clonal amniotic fluid stem cell lines as new tools to investigate molecular and cell biological consequences of human natural occurring disease causing mutations is discussed.
未来,对不同人类干细胞的特性鉴定和分离将有助于对细胞分化过程进行详细的分子研究,并为多种疾病建立新的治疗理念。自大约10年前首次成功分离和培养人类胚胎干细胞以来,其在研究和治疗中的应用一直受到复杂伦理考量以及未分化胚胎干细胞移植到患者体内后发生恶性发展风险的限制。成体干细胞在伦理上是可接受的,且肿瘤发生风险较低。然而,它们的分化潜能和增殖能力有限。大约4年前,羊水干细胞的发现开启了一个新的、有前景的干细胞研究领域,羊水干细胞表达多能干细胞的特异性标志物Oct-4,具有高增殖能力和多系分化潜能。在此期间,羊水干细胞已被证明具有分化为所有三个胚胎胚层细胞的潜力。这些干细胞在体内不会形成肿瘤,也不会引发与人类胚胎干细胞相关的伦理问题。进一步的研究将揭示羊水干细胞是否真的代表一种比成体干细胞和胚胎干细胞都更具优势的中间细胞类型。本文还讨论了生成克隆羊水干细胞系作为研究人类自然发生的致病突变的分子和细胞生物学后果的新工具的方法。