From hematopoiesis to neuropoiesis: Evidence of overlapping genetic programs

被引:230
作者
Terskikh, AV
Easterday, MC
Li, LH
Hood, L
Kornblum, HI
Geschwind, DH
Weissman, IL
机构
[1] Stanford Univ, Sch Med, Dept Pathol, Beckman Ctr B259, Stanford, CA 94305 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Mol & Med Pharmacol & Pediat, Los Angeles, CA 90095 USA
[3] Univ Washington, Dept Mol Biotechnol, Seattle, WA 98195 USA
[4] Univ Calif Los Angeles, Sch Med, Neurogenet Program, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Sch Med, Dept Neurol, Reed Neurol Res Ctr, Los Angeles, CA 90095 USA
关键词
D O I
10.1073/pnas.131200898
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
It is reasonable to propose that gene expression profiles of purified stem cells could give clues for the molecular mechanisms of stem cell behavior. We took advantage of cDNA subtraction to identify a set of genes selectively expressed in mouse adult hematopoietic stem cells (HsC) as opposed to bone marrow (BM). Analysis of HSC-enriched genes revealed several key regulatory gene candidates, including two novel seven transmembrane (7TM) receptors, Furthermore, by using cDNA microarray techniques we found a large set of HSC-enriched genes that are expressed in mouse neurospheres (a population greatly enriched for neural progenitor cells), but not present in terminally differentiated neural cells. In situ hybridization demonstrated that many of them, including one HSC-enriched 7TM receptor, were selectively expressed in the germinal zones of fetal and adult brain, the regions harboring mouse neural stem cells. We propose that at least some of the transcripts that are selectively and commonly expressed in two or more types of stem cells define a functionally conserved group of genes evolved to participate in basic stem cell functions, including stem cell self-renewal.
引用
收藏
页码:7934 / 7939
页数:6
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