Increasing Doublecortin Expression Promotes Migration of Human Embryonic Stem Cell-Derived Neurons

被引:19
|
作者
Filipovic, Radmila [1 ]
Kumar, Saranya Santhosh [1 ]
Fiondella, Chris [1 ]
Loturco, Joseph [1 ]
机构
[1] Univ Connecticut, Dept Physiol & Neurobiol, Storrs, CT 06268 USA
关键词
Human embryonic stem cells; Neuronal progenitor; Proliferation; Migration; Radial glia; MICROTUBULE-ASSOCIATED PROTEIN; RADIAL GLIA; PIGGYBAC TRANSPOSON; CEREBRAL-CORTEX; GENE-TRANSFER; IN-VIVO; SUBVENTRICULAR ZONE; NEURAL PRECURSORS; RNA INTERFERENCE; RAT NEOCORTEX;
D O I
10.1002/stem.1162
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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 (1) 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. STEM CELLS 2012;30:1852-1862
引用
收藏
页码:1852 / 1862
页数:11
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