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Generation of dopaminergic neurons and pigmented epithelia from primate ES cells by stromal cell-derived inducing activity
Author(s) -
Hiroshi Kawasaki,
Hirofumi Suemori,
Kenji Mizuseki,
Kiichi Watanabe,
Fumi Urano,
Hiroshi Ichinose,
Masatoshi Haruta,
Masayo Takahashi,
Kanako Yoshikawa,
ShinIchi Nishikawa,
Norio Nakatsuji,
Yoshiki Sasai
Publication year - 2002
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.032662199
Subject(s) - embryonic stem cell , biology , retinitis pigmentosa , dopaminergic , transplantation , microbiology and biotechnology , stromal cell , stem cell , cellular differentiation , retina , dopamine , neuroscience , cancer research , medicine , genetics , gene
We previously identified a stromal cell-derived inducing activity (SDIA), which induces differentiation of neural cells, including midbrain tyrosine hydroxylase-positive (TH(+)) dopaminergic neurons, from mouse embryonic stem cells. We report here that SDIA induces efficient neural differentiation also in primate embryonic stem cells. Induced neurons contain TH(+) neurons at a frequency of 35% and produce a significant amount of dopamine. Interestingly, differentiation of TH(+) neurons from undifferentiated embryonic cells occurs much faster in vitro (10 days) than it does in the embryo (approximately 5 weeks). In addition, 8% of the colonies contain large patches of Pax6(+)-pigmented epithelium of the retina. The SDIA method provides an unlimited source of primate cells for the study of pathogenesis, drug development, and transplantation in degenerative diseases such as Parkinson's disease and retinitis pigmentosa.

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