Adult SVZ Lineage Cells Home to and Leave the Vascular Niche via Differential Responses to SDF1/CXCR4 Signaling

被引:305
作者
Kokovay, Erzsebet [1 ,2 ]
Goderie, Susan [1 ]
Wang, Yue [1 ]
Lotz, Steve [1 ]
Lin, Gang [3 ]
Sun, Yu [4 ]
Roysam, Badrinath [3 ]
Shen, Qin [1 ,2 ]
Temple, Sally [1 ,2 ]
机构
[1] New York Neural Stem Cell Inst, Rensselaer, NY 12144 USA
[2] Albany Med Coll, Ctr Neuropharmacol & Neurosci, Albany, NY 12208 USA
[3] Rensselaer Polytech Inst, Rensselaer, NY 12180 USA
[4] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
关键词
NEURAL STEM-CELLS; POSTNATAL SUBVENTRICULAR ZONE; CHEMOKINE RECEPTOR CXCR4; PROGENITOR CELLS; NEUROBLAST MIGRATION; NEURONAL MIGRATION; MAMMALIAN BRAIN; NEUROGENESIS; STROKE; PRECURSORS;
D O I
10.1016/j.stem.2010.05.019
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Neural progenitor cells (NPCs) in the adult subventricular zone (SVZ) are associated with ependymal and vasculature niches, which regulate stem cell self-renewal and differentiation. Activated Type B stem cells and their progeny, the transit-amplifying type C cells, which express EGFR, are most highly associated with vascular cells, indicating that this niche supports lineage progression. Here, we show that proliferative SVZ progenitor cells home to endothelial cells in a stromal-derived factor 1 (SDF1)- and CXC chemokine receptor 4 (CXCR4)-dependent manner. We show that SDF1 strongly upregulates EGFR and alpha 6 integrin in activated type B and type C cells, enhancing their activated state and their ability to bind laminin in the vascular niche. SDF1 increases the motility of type A neuroblasts, which migrate from the SVZ toward the olfactory bulb. Thus, differential responses to SDF1 can regulate progenitor cell occupancy of and exit from the adult SVZ vascular niche.
引用
收藏
页码:163 / 173
页数:11
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