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A Critical Period in Cortical Interneuron Neurogenesis in Down Syndrome Revealed by Human Neural Progenitor Cells
Author(s) -
Anita Bhattacharyya,
Erin McMillan,
Serene I. Chen,
Kyle Wallace,
Clive N. Svendsen
Publication year - 2009
Publication title -
developmental neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.893
H-Index - 82
eISSN - 1421-9859
pISSN - 0378-5866
DOI - 10.1159/000236899
Subject(s) - neurogenesis , interneuron , progenitor cell , neuroscience , progenitor , biology , neural stem cell , population , neurosphere , cerebral cortex , period (music) , stem cell , cellular differentiation , microbiology and biotechnology , adult stem cell , inhibitory postsynaptic potential , medicine , gene , genetics , physics , environmental health , acoustics
Down syndrome (DS) is a developmental disorder whose mental impairment is due to defective cortical development. Human neural progenitor cells (hNPCs) derived from fetal DS cortex initially produce normal numbers of neurons, but generate fewer neurons with time in culture, similar to the pattern of neurogenesis that occurs in DS in vivo. Microarray analysis of DS hNPCs at this critical time reveals gene changes indicative of defects in interneuron progenitor development. In addition, dysregulated expression of many genes involved in neural progenitor cell biology points to changes in the progenitor population and subsequent reduction in interneuron neurogenesis. Delineation of a critical period in interneuron development in DS provides a foundation for investigation of the basis of reduced neurogenesis in DS and defines a time when these progenitor cells may be amenable to therapeutic treatment.

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