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Prakash, N. ; Wurst, W.

Genetic networks controlling the development of midbrain dopaminergic neurons.

J. Physiol. 575, 403-410 (2006)
DOI
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Recent data have substantially advanced our understanding of midbrain dopaminergic neuron development. Firstly, a Wnt1-regulated genetic network, including Otx2 and Nkx2-2, and a Shh-controlled genetic cascade, including Lmx1a, Msx1 and Nkx6-1, have been unravelled, acting in parallel or sequentially to establish a territory competent for midbrain dopaminergic precursor production at relatively early stages of neural development. Secondly, the same factors (Wnt1 and Lmx1a/Msx1) appear to regulate midbrain dopaminergic and/or neuronal fate specification in the postmitotic progeny of these precursors by controlling the expression of midbrain dopaminergic-specific and/or general proneural factors at later stages of neural development. For the first time, early inductive events have thus been linked to later differentiation processes in midbrain dopaminergic neuron development. Given the pivotal importance of this neuronal population for normal function of the human brain and its involvement in severe neurological and psychiatric disorders such as Parkinson's Disease, these advances open new prospects for potential stem cell-based therapies. We will summarize these new findings in the overall context of midbrain dopaminergic neuron development in this review.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Animals; Cell Differentiation/genetics*; Dopamine/metabolism*; Gene Expression Regulation; Developmental/genetics*; Gene Expression Regulation; Developmental/physiology; Hedgehog Proteins; Mesencephalon/cytology*; Mesencephalon/embryology; Mesencephalon/
Sprache englisch
Veröffentlichungsjahr 2006
HGF-Berichtsjahr 0
ISSN (print) / ISBN 0928-4257
e-ISSN 1769-7115
Zeitschrift Journal of Physiology - Paris
Quellenangaben Band: 575, Heft: 2, Seiten: 403-410 Artikelnummer: , Supplement: ,
Verlag Elsevier
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Developmental Genetics (IDG)
POF Topic(s) 30204 - Cell Programming and Repair
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-500500-001
DOI 10.1113/jphysiol.2006.113464
Erfassungsdatum 2006-10-27
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