Altered nuclear transfer - A way forward for embryonic stem cell research

被引:15
作者
Hurlbut, William B. [1 ]
机构
[1] Stanford Univ, Med Ctr, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
来源
STEM CELL REVIEWS | 2005年 / 1卷 / 04期
关键词
D O I
10.1385/SCR:1:4:293
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The present conflict over the moral status of the human embryo reflects deep differences in our basic convictions and is unlikely to be resolved through deliberation or debate. While there are currently no federally legislated constraints on the use of private funds for this research, there is a consensus opinion in the scientific community that without NIH support for newly created embryonic stem cell lines, progress in this important realm of research will be severely constrained. A May, 2005, report by the President's Council on Bioethics, "Alternative Sources of Pluripotent Stem Cells," outlines several proposals for obtaining pluripotent stem cells without the destruction of human embryos. One of these methods, Altered Nuclear Transfer, proposes to use the technology of somatic cell nuclear transfer (SCNT), but with a preemptive genetic or epigenetic alteration that precludes the integrated and coordinated organization essential for natural embryogenesis. Drawing on insights from systems biology, the distinction between totipotency (capacity to form a whole organism) and pluripotency (capacity to form all the cell types) is explored. The implications of this distinction are used to discuss the moral arguments for the inviolability of nascent human life and the moral standing of entities with only partial and unorganized developmental potential. Away forward is proposed that may open positive avenues of advance in both stem cell research and a broader arena of research in developmental biology.
引用
收藏
页码:293 / 300
页数:8
相关论文
共 13 条
[1]  
BEHR B, COMMUNICATION
[2]   ES cells derived from cloned and fertilized blastocysts are transcriptionally and functionally indistinguishable [J].
Brambrink, T ;
Hochedlinger, K ;
Bell, G ;
Jaenisch, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (04) :933-938
[3]   Embryonic and extraembryonic stem cell lines derived from single mouse blastomeres [J].
Chung, Y ;
Klimanskaya, I ;
Becker, S ;
Marh, J ;
Lu, SJ ;
Johnson, J ;
Meisner, L ;
Lanza, R .
NATURE, 2006, 439 (7073) :216-219
[4]   Nuclear reprogramming of somatic cells after fusion with human embryonic stem cells [J].
Cowan, CA ;
Atienza, J ;
Melton, DA ;
Eggan, K .
SCIENCE, 2005, 309 (5739) :1369-1373
[5]   RETRACTED: Cdx2 gene expression and trophectoderm lineage specification in mouse embryos (Retracted article. See vol 317, pg 450, 2007) [J].
Deb, K ;
Sivaguru, M ;
Yong, HY ;
Roberts, RM .
SCIENCE, 2006, 311 (5763) :992-996
[6]   PERSONHOOD AND CONCEPTION EVENT [J].
JOYCE, RE .
NEW SCHOLASTICISM, 1978, 52 (01) :97-109
[7]   Birth of parthenogenetic mice that can develop to adulthood [J].
Kono, T ;
Obata, Y ;
Wu, QL ;
Niwa, K ;
Ono, Y ;
Yamamoto, Y ;
Park, ES ;
Seo, JS ;
Ogawa, H .
NATURE, 2004, 428 (6985) :860-864
[8]   Generation of nuclear transfer-derived pluripotent ES cells from cloned Cdx2-deficient blastocysts [J].
Meissner, A ;
Jaenisch, R .
NATURE, 2006, 439 (7073) :212-215
[9]   Role for sperm in spatial patterning of the early mouse embryo [J].
Piotrowska, K ;
Zernicka-Goetz, M .
NATURE, 2001, 409 (6819) :517-521
[10]  
*PRES OCUNC BIOETH, WHIT PAP ALT SOURC P