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Steps Toward Safe Cell Therapy Using Induced Pluripotent Stem Cells
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Yoshida, Kenji
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Keio Univ, Sch Med, Dept Physiol, Tokyo 1608582, Japan
Keio Univ, Sch Med, Kanrinmaru Project, Tokyo 1608582, Japan
Dainippon Sumitomo Pharma, Genom Sci Lab, Osaka, Japan Keio Univ, Sch Med, Dept Physiol, Tokyo 1608582, Japan

Okada, Yohei
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Keio Univ, Sch Med, Dept Physiol, Tokyo 1608582, Japan
Keio Univ, Sch Med, Kanrinmaru Project, Tokyo 1608582, Japan Keio Univ, Sch Med, Dept Physiol, Tokyo 1608582, Japan

Tsuji, Osahiko
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Keio Univ, Sch Med, Dept Physiol, Tokyo 1608582, Japan
Keio Univ, Sch Med, Dept Orthoped Surg, Tokyo 1608582, Japan Keio Univ, Sch Med, Dept Physiol, Tokyo 1608582, Japan

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Ikeda, Eiji
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Yamaguchi Univ, Grad Sch Med, Dept Pathol, Yamaguchi, Japan Keio Univ, Sch Med, Dept Physiol, Tokyo 1608582, Japan

Yamanaka, Shinya
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Kyoto Univ, Ctr iPS Cell Res & Applicat, Kyoto, Japan Keio Univ, Sch Med, Dept Physiol, Tokyo 1608582, Japan

Miura, Kyoko
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Keio Univ, Sch Med, Dept Physiol, Tokyo 1608582, Japan Keio Univ, Sch Med, Dept Physiol, Tokyo 1608582, Japan
机构:
[1] Keio Univ, Sch Med, Dept Physiol, Tokyo 1608582, Japan
[2] Keio Univ, Sch Med, Dept Orthoped Surg, Tokyo 1608582, Japan
[3] Keio Univ, Sch Med, Kanrinmaru Project, Tokyo 1608582, Japan
[4] Yamaguchi Univ, Grad Sch Med, Dept Pathol, Yamaguchi, Japan
[5] Kyoto Univ, Ctr iPS Cell Res & Applicat, Kyoto, Japan
[6] Dainippon Sumitomo Pharma, Genom Sci Lab, Osaka, Japan
关键词:
induced pluripotent stem cell;
neural stem/progenitor cell;
transplantation;
spinal cord injury;
HUMAN SOMATIC-CELLS;
SPINAL-CORD-INJURY;
FUNCTIONAL RECOVERY;
SENDAI-VIRUS;
HUMAN FIBROBLASTS;
IN-VIVO;
MOUSE;
GENERATION;
DIFFERENTIATION;
CARDIOMYOCYTES;
D O I:
10.1161/CIRCRESAHA.111.256149
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
The enthusiasm for producing patient-specific human embryonic stem cells using somatic nuclear transfer has somewhat abated in recent years because of ethical, technical, and political concerns. However, the interest in generating induced pluripotent stem cells (iPSCs), in which pluripotency can be obtained by transcription factor transduction of various somatic cells, has rapidly increased. Human iPSCs are anticipated to open enormous opportunities in the biomedical sciences in terms of cell therapies for regenerative medicine and stem cell modeling of human disease. On the other hand, recent reports have emphasized the pitfalls of iPSC technology, including the potential for genetic and epigenetic abnormalities, tumorigenicity, and immunogenicity of transplanted cells. These constitute serious safety-related concerns for iPSC-based cell therapy. However, preclinical data supporting the safety and efficacy of iPSCs are also accumulating. In this Review, recent achievements and future tasks for safe iPSC-based cell therapy are summarized, using regenerative medicine for repair strategies in the damaged central nervous system (CNS) as a model. Insights on safety and preclinical use of iPSCs in cardiovascular repair model are also discussed. (Circ Res. 2013;112:523-533.)
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页码:523 / 533
页数:11
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h-index: 0
机构:
Shandong Univ, Sch Med, Dept Histol & Embryol, Ke Lab Minist Educ Expt Teratol, Jinan 250012, Shandong, Peoples R China Shandong Univ, Sch Med, Dept Histol & Embryol, Ke Lab Minist Educ Expt Teratol, Jinan 250012, Shandong, Peoples R China
[10]
The evolving biology of small molecules: controlling cell fate and identity
[J].
Efe, Jem A.
;
Ding, Sheng
.
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES,
2011, 366 (1575)
:2208-2221

Efe, Jem A.
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h-index: 0
机构:
Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA

Ding, Sheng
论文数: 0 引用数: 0
h-index: 0
机构:
Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA