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Journal of Neurochemistry
Article . 2002 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
Proceedings of the National Academy of Sciences
Article . 2001 . Peer-reviewed
Data sources: Crossref
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From hematopoiesis to neuropoiesis: Evidence of overlapping genetic programs

Authors: A V, Terskikh; M C, Easterday; L, Li; L, Hood; H I, Kornblum; D H, Geschwind; I L, Weissman;

From hematopoiesis to neuropoiesis: Evidence of overlapping genetic programs

Abstract

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 situhybridization 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.

Related Organizations
Keywords

Neurons, Mice, Gene Expression Regulation, Stem Cells, Molecular Sequence Data, Animals, Cell Differentiation, Cell Lineage, Hematopoietic Stem Cells, Hematopoiesis

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
258
Top 10%
Top 1%
Top 0.1%
bronze
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