
STEM CELLS – A BASIS FOR THERAPY IN THE FUTURE Yosifova A, Toncheva D* *Corresponding Author: Professor Draga Toncheva, Department of Medical Genetics, Medical University Sofia, 2 Zdrave str, 1431 Sofia, Bulgaria; Tel./Fax: +359-2-952-03-57; E-mail: dragatoncheva@yahoo.com
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INTRODUCTION
The discovery of mouse embryonic stem (ES) cells in 1981 [1,2] provided the paradigm and much of the technology for the discovery of human embryonic stem cells. Research on ES cells evolved out of work on mouse teratocarcinomas that consist of a remarkable array of somatic tissues juxtaposed together in a disorganized fashion. The origin of such tumors from germ cells in mice provided the concept of a stem cell (the embryonal carcinoma or EC cell) that can give rise to the multiple types of tissue found in tumors [3]. This field of research expanded considerably with the generation of chimaeric mice by blastocyst injection of EC cells [4]. However, these cells contained chromosomal abnormalities and often had a limited capacity to differentiate into multiple tissue types [5]. Since teratocarcinomas can also be induced by grafting blastocysts to ectopic sites, it was reasoned [2], that it might be possible to derive pluripotent cell lines directly from blastocysts rather than from tumors. Evans and Kaufman [1] and Martin [2] independently obtained a cell line with properties of mouse teratocarcinoma stem cells including pluripotency, cell morphology, and the ability to form teratocarcinomas when injected into mice. The first human ES cells were isolated in 1998 from embryos created through in vitro fertilization (IVF) [6].
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