Literature DB >> 22753232

Increasing doublecortin expression promotes migration of human embryonic stem cell-derived neurons.

Radmila Filipovic1, Saranya Santhosh Kumar, Chris Fiondella, Joseph Loturco.   

Abstract

Human embryonic stem cell-derived neuronal progenitors (hNPs) provide a potential source for cellular replacement following neurodegenerative diseases. One of the greatest challenges for future neuron replacement therapies will be to control extensive cell proliferation and stimulate cell migration of transplanted cells. The doublecortin (DCX) gene encodes the protein DCX, a microtubule-associated protein essential for the migration of neurons in the human brain. In this study, we tested whether increasing the expression of DCX in hNPs would favorably alter their proliferation and migration. Migration and proliferation of hNPs was compared between hNPs expressing a bicistronic DCX/IRES-GFP transgene and those expressing a green fluorescent protein (GFP) transgene introduced by piggyBac-mediated transposition. The DCX-transfected hNPs showed a significant decrease in their proliferation and migrated significantly further on two different substrates, Matrigel and brain slices. Additionally, a dense network of nestin-positive (+) and vimentin+ fibers were found to extend from neurospheres transplanted onto brain slices, and this fiber growth was increased from neurospheres containing DCX-transfected hNPs. In summary, our results show that increased DCX expression inhibits proliferation and promotes migration of hNPs.
Copyright © 2012 AlphaMed Press.

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Year:  2012        PMID: 22753232      PMCID: PMC3951429          DOI: 10.1002/stem.1162

Source DB:  PubMed          Journal:  Stem Cells        ISSN: 1066-5099            Impact factor:   6.277


  54 in total

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9.  piggyBac-based mosaic screen identifies a postmitotic function for cohesin in regulating developmental axon pruning.

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  3 in total

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  3 in total

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