Publikationsdatum:
2004-02-14
Beschreibung:
Somatic cell nuclear transfer (SCNT) technology has recently been used to generate animals with a common genetic composition. In this study, we report the derivation of a pluripotent embryonic stem (ES) cell line (SCNT-hES-1) from a cloned human blastocyst. The SCNT-hES-1 cells displayed typical ES cell morphology and cell surface markers and were capable of differentiating into embryoid bodies in vitro and of forming teratomas in vivo containing cell derivatives from all three embryonic germ layers in severe combined immunodeficient mice. After continuous proliferation for more than 70 passages, SCNT-hES-1 cells maintained normal karyotypes and were genetically identical to the somatic nuclear donor cells. Although we cannot completely exclude the possibility that the cells had a parthenogenetic origin, imprinting analyses support a SCNT origin of the derived human ES cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hwang, Woo Suk -- Ryu, Young June -- Park, Jong Hyuk -- Park, Eul Soon -- Lee, Eu Gene -- Koo, Ja Min -- Jeon, Hyun Yong -- Lee, Byeong Chun -- Kang, Sung Keun -- Kim, Sun Jong -- Ahn, Curie -- Hwang, Jung Hye -- Park, Ky Young -- Cibelli, Jose B -- Moon, Shin Yong -- New York, N.Y. -- Science. 2004 Mar 12;303(5664):1669-74. Epub 2004 Feb 12.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉College of Veterinary Medicine, Seoul National University, Seoul 151-742, Korea. hwangws@snu.ac.kr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14963337" target="_blank"〉PubMed〈/a〉
Schlagwort(e):
Animals
;
Biomarkers/analysis
;
Blastocyst/*cytology
;
Cell Differentiation
;
*Cell Line
;
*Cloning, Organism
;
Culture Media
;
Culture Techniques
;
DNA Fingerprinting
;
Embryo, Mammalian/*cytology
;
Female
;
Genomic Imprinting
;
Humans
;
Karyotyping
;
Male
;
Mice
;
Mice, SCID
;
Nuclear Transfer Techniques
;
Oocyte Donation
;
Ovarian Follicle/cytology
;
Parthenogenesis
;
Pluripotent Stem Cells/chemistry/*cytology
;
Reverse Transcriptase Polymerase Chain Reaction
;
Tandem Repeat Sequences
;
Teratoma/etiology/pathology
;
Testicular Neoplasms/etiology/pathology
Print ISSN:
0036-8075
Digitale ISSN:
1095-9203
Thema:
Biologie
,
Chemie und Pharmazie
,
Informatik
,
Medizin
,
Allgemeine Naturwissenschaft
,
Physik
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