| Literature DB >> 16182609 |
Xiao-Gang Li1, Takashi Okada, Mika Kodera, Yuko Nara, Naomi Takino, Chieko Muramatsu, Kunihiko Ikeguchi, Fumi Urano, Hiroshi Ichinose, Daniel Metzger, Pierre Chambon, Imaharu Nakano, Keiya Ozawa, Shin-Ichi Muramatsu.
Abstract
Regulation of gene expression is necessary to avoid possible adverse effects of gene therapy due to excess synthesis of transgene products. To reduce transgene expression, we developed a viral vector-mediated somatic regulation system using inducible Cre recombinase. A recombinant adeno-associated virus (AAV) vector expressing Cre recombinase fused to a mutated ligand-binding domain of the estrogen receptor alpha (CreER(T2)) was delivered along with AAV vectors expressing dopamine-synthesizing enzymes to rats of a Parkinson disease model. Treatment with 4-hydroxytamoxifen, a synthetic estrogen receptor modulator, activated Cre recombinase within the transduced neurons and induced selective excision of the tyrosine hydroxylase (TH) coding sequence flanked by loxP sites, leading to a reduction in transgene-mediated dopamine synthesis. Using this strategy, aromatic L-amino acid decarboxylase (AADC) activity was retained so that l-3,4-dihydroxyphenylalanine (L-dopa), a substrate for AADC, could be converted to dopamine in the striatum and the therapeutic effects of L-dopa preserved, even after reduction of TH expression in the case of dopamine overproduction. Our data demonstrate that viral vector-mediated inducible Cre recombinase can serve as an in vivo molecular switch, allowing spatial and temporal control of transgene expression, thereby potentially increasing the safety of gene therapy.Entities:
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Year: 2005 PMID: 16182609 DOI: 10.1016/j.ymthe.2005.08.009
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454