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Dopamine neuron precursors within the developing human mesencephalon show radial glial characteristics
Authors:Josephine B Hebsgaard  Jenny Nelander  Hanna Sabelström  Marie E Jönsson  Simon Stott  Malin Parmar
Institution:1. Department of Experimental Medical Science, Wallenberg Neuroscience Center, Lund University, Lund, Sweden;2. Lund Strategic Center for Stem Cell Biology and Cell Therapy, Wallenberg Neuroscience Center, Lund University, Lund, Sweden;3. Department of Cell and Molecular Biology, Medical Nobel Institute, Karolinska Institute, Stockholm, Sweden;4. Division of Developmental Neurobiology, MRC National Institute for Medical Research, The Ridgeway, London NW7 1AA, United Kingdom
Abstract:Specification and differentiation of neural precursors into dopaminergic neurons within the ventral mesencephalon has been subject to much attention due to the implication of dopaminergic neurons in Parkinson's disease and the perspective of generating sources of therapeutically active cells to be used for cell replacement therapy for the disease. However, despite intensive research efforts, little is known about the characteristics of the dopamine neuron progenitors in human. We show that the dopamine neuron determinant LMX1a is expressed in the diencephalic and mesencephalic dopaminergic neuron domains during human development. Within the mesencephalon, LMX1a is expressed in the dopaminergic neurons and their progenitors located in the ventricular zone of the floor plate region. Furthermore, the neural progenitors in the developing human ventral mesencephalon have a radial morphology and express the radial glial markers Vimentin and BLBP. These radial glia are mitotic and act as precursors for the dopaminergic neurons. Finally, we show that progenitors isolated from the human ventral mesencephalon maintain their radial glial characteristics and neurogenic capacity after expansion in vitro, making them a promising future source of cells to be used in cell replacement therapy for Parkinson's disease. © 2009 Wiley‐Liss, Inc.
Keywords:Parkinson's disease  neurogenesis  neural stem cell cultures  transplantation
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