The Molecular Profiles of Neural Stem Cell Niche in the Adult Subventricular Zone

被引:46
作者
Lee, Cheol [2 ]
Hu, Jingqiong [1 ]
Ralls, Sherry [2 ]
Kitamura, Toshio [3 ]
Loh, Y. Peng [4 ]
Yang, Yanqin [5 ]
Mukouyama, Yohsuke [1 ]
Ahn, Sohyun [2 ]
机构
[1] NHLBI, Lab Stem Cell & Neurovasc Biol, Genet & Dev Biol Ctr, NIH, Bethesda, MD 20892 USA
[2] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Program Genom Differentiat, NIH, Bethesda, MD USA
[3] Univ Tokyo, Inst Med Sci, Div Cellular Therapy, Adv Clin Res Ctr, Tokyo, Japan
[4] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Cellular Neurobiol Sect, Program Dev Neurosci, NIH, Bethesda, MD USA
[5] NHLBI, DNA Sequencing & Genom Core Facil, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
GENE-EXPRESSION ANALYSIS; BINDING GROWTH-FACTOR; CARBOXYPEPTIDASE E; THYROID-HORMONES; PRECURSOR CELLS; VASCULAR NICHE; CHOROID-PLEXUS; DENTATE GYRUS; SELF-RENEWAL; RADIAL GLIA;
D O I
10.1371/journal.pone.0050501
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neural stem cells (NSCs) reside in a unique microenvironment called the neurogenic niche and generate functional new neurons. The neurogenic niche contains several distinct types of cells and interacts with the NSCs in the subventricular zone (SVZ) of the lateral ventricle. While several molecules produced by the niche cells have been identified to regulate adult neurogenesis, a systematic profiling of autocrine/paracrine signaling molecules in the neurogenic regions involved in maintenance, self-renewal, proliferation, and differentiation of NSCs has not been done. We took advantage of the genetic inducible fate mapping system (GIFM) and transgenic mice to isolate the SVZ niche cells including NSCs, transit-amplifying progenitors (TAPs), astrocytes, ependymal cells, and vascular endothelial cells. From the isolated cells and microdissected choroid plexus, we obtained the secretory molecule expression profiling (SMEP) of each cell type using the Signal Sequence Trap method. We identified a total of 151 genes encoding secretory or membrane proteins. In addition, we obtained the potential SMEP of NSCs using cDNA microarray technology. Through the combination of multiple screening approaches, we identified a number of candidate genes with a potential relevance for regulating the NSC behaviors, which provide new insight into the nature of neurogenic niche signals.
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页数:18
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