In vitro and in vivo enhanced generation of human A9 dopamine neurons from neural stem cells by Bcl-XL
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Human neural stem cells derived from the ventral mesencephalon (VM) are powerful research tools and candidates for cell therapies in Parkinson disease. Previous studies with VM dopaminergic neuron (DAn) precursors indicated poor growth potential and unstable phenotypical properties. Using the model cell line hVM1 (human ventral mesencephalic neural stem cell line 1; a new human fetal VM stem cell line), we have found that Bcl-XL enhances the generation of DAn from VM human neural stem cells. Mechanistically, Bcl-XL not only exerts the expected antiapoptotic effect but also induces proneural (NGN2 and NEUROD1) and dopamine-related transcription factors, resulting in a high yield of DAn with the correct phenotype of substantia nigra pars compacta (SNpc). The expression of key genes directly involved in VM/SNpc dopaminergic patterning, differentiation, and maturation (EN1, LMX1B, PITX3, NURR1, VMAT2, GIRK2, and dopamine transporter) is thus enhanced by Bcl-XL. These effects on neurogenesis occur in parallel to a decrease in glia generation. These in vitro Bcl-XL effects are paralleled in vivo, after transplantation in hemiparkinsonian rats, where hVM1-Bcl-XL cells survive, integrate, and differentiate into DAn, alleviating behavioral motor asymmetry. Bcl-XL then allows for human fetal VM stem cells to stably generate mature SNpc DAn both in vitro and in vivo and is thus proposed as a helpful factor for the development of cell therapies for neurodegenerative conditions, Parkinson disease in particular. © 2010 by The American Society for Biochemistry and Molecular Biology, Inc.
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Anti-apoptotic effects; Cell lines; Cell therapy; Dopamine neurons; Dopamine transporters; Dopaminergic neurons; Growth potential; High yield; In-vitro; In-vivo; Neural stem cell; Neurodegenerative; Neurogenesis; Parkinson disease; Research tools; Stem cell; Substantia nigra; Brain; Cell culture; Neurons; Transcription; Transcription factors; Stem cells; cell protein; dopamine transporter; G protein coupled inwardly rectifying potassium channel 2; neurogenic differentiation factor; neurogenin 2; nuclear receptor related factor 1; protein bcl xl; protein EN1; protein LMX1B; unclassified drug; vesicular monoamine transporter 2; dopamine; protein bcl x; animal experiment; animal model; article; cell maturation; cell protection; cell survival; controlled study; degenerative disease; dopaminergic nerve cell; fetus; gene expression regulation; glia cell; human; human cell; in vitro study; in vivo study; motor performance; nerve cell differentiation; neural stem cell; neural stem cell transplantation; nonhuman; parkinsonism; phenotype; priority journal; protein analysis; protein function; protein induction; rat; substantia nigra; animal; animal behavior; apoptosis; cell differentiation; cell line; cell membrane potential; cytology; disease model; female; metabolism; nerve cell; Parkinson disease; Sprague Dawley rat; stem cell; Rattus; Animals; Apoptosis; bcl-X Protein; Behavior, Animal; Cell Differentiation; Cell Line; Disease Models, Animal; Dopamine; Female; Humans; Membrane Potentials; Neurons; Parkinson Disease; Phenotype; Rats; Rats, Sprague-Dawley; Stem Cells; Substantia Nigra
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