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Efficient establishment of human embryonic stem cell lines and long-term maintenance with stable karyotype by enzymatic bulk passage
Author(s): Suemori H, Yasuchika K, Hasegawa K, Fujioka T, Tsuneyoshi N, Nakatsuji N
Source: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS    Volume: 345    Issue: 3    Pages: 926-932    Published: JUL 7 2006  
Times Cited: 45     References: 19     
Abstract: Human ES (hES) cell lines are considered to be a valuable resource for medical research and for applications in cell therapy and drug discovery. For such utilization of hES cells to be realized, however, protocols involved in the use of hES cells, such as those for establishment, propagation, and cryopreservation, have still to be improved. Here, we report on an efficient method for the establishment of hES cell lines and its detailed characterization. Additionally, we developed a new bulk-passaging technique that preserves the karyotypic integrity of hES cell lines when maintained in culture for up to 2 years. Finally, we show that a simplified vitrification cryopreservation technique is vastly superior to standard slow-cooling methods with respect to cell viability. These results provide valuable information that will assist in achieving the goal of the large-scale hES cell culture required for the application of hES cells to disease therapy. (c) 2006 Elsevier Inc. All rights reserved.
Document Type: Article
Language: English
Reprint Address: Suemori, H (reprint author), Kyoto Univ, Inst Frontier Med Sci, Stem Cell Res Ctr, Lab Embryon Stem Cell Res,Sakyo Ku, 53 Kawahara Cho, Kyoto 6068507, Japan
Addresses:
1. Kyoto Univ, Inst Frontier Med Sci, Stem Cell Res Ctr, Lab Embryon Stem Cell Res,Sakyo Ku, Kyoto 6068507, Japan
2. Kyoto Univ, Isnt Frontier Med Sci, Dept Dev & Differentiat, Sakyo Ku, Kyoto 6068507, Japan
Publisher: ACADEMIC PRESS INC ELSEVIER SCIENCE, 525 B ST, STE 1900, SAN DIEGO, CA 92101-4495 USA
Subject Category: Biochemistry & Molecular Biology; Biophysics
IDS Number: 054AA
ISSN: 0006-291X
DOI: 10.1016/j.bbrc.2006.04.135
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