Neural stem cell heterogeneity demonstrated by molecular phenotyping of clonal neurospheres

被引:257
作者
Suslov, ON
Kukekov, VG
Ignatova, TN
Steindler, DA
机构
[1] Univ Florida, Coll Med, McKnight Brain Inst, Shands Canc Ctr,Dept Neurosci, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, McKnight Brain Inst, Shands Canc Ctr,Dept Neurosurg, Gainesville, FL 32610 USA
[3] Univ Florida, Program Stem Cell Biol & Regenerat Med, Gainesville, FL 32610 USA
关键词
stem cell; cDNA panel; microarray; iterative algorithm; temporal profiling;
D O I
10.1073/pnas.212525299
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) in vitro are able to generate clonal structures, "neurospheres," that exhibit intra-clonal neural cell-lineage diversity; i.e., they contain, in addition to NSCs, neuronal and glial progenitors in different states of differentiation. The present study focuses on a subset of neurospheres derived from fresh clinical specimens of human brain by using an in vitro system that relies on particular growth factors, serum, and anchorage withdrawal. Thirty individual and exemplary cDNA libraries from these neurosphere clones were clustered and rearranged within a panel after characterization of differentially expressed transcripts. The molecular phenotypes that were obtained indicate that clonogenic NSCs in our in vitro system are heterogeneous, with subsets reflecting distinct neural developmental commitments. This approach is useful for the sorting and expansion of NSCs and facilitates the discovery of genes involved in cell proliferation, communication, fate control, and differentiation.
引用
收藏
页码:14506 / 14511
页数:6
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