Article
Lunatic fringe causes expansion and increased neurogenesis of trunk neural tube and neural crest populations.
Division of Biology, 139-74, California Institute of Technology, Pasadena, USA.
Neuron Glia Biology (impact factor:
1.34).
02/2007;
3(2):93-103.
DOI:10.1017/S1740925X07000683
Source: PubMed
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Article: rax, Hes1, and notch1 promote the formation of Müller glia by postnatal retinal progenitor cells.
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ABSTRACT: We are interested in the mechanisms of glial cell development in the vertebrate central nervous system. We have identified genes that can direct the formation of glia in the retina. rax, a homeobox gene, Hes1, a basic helix-loop-helix gene, and notch1, a transmembrane receptor gene, are expressed in retinal progenitor cells, downregulated in differentiated neurons, and expressed in Müller glia. Retroviral transduction of any of these genes resulted in expression of glial markers. In contrast, misexpression of a dominant-negative Hes1 gene reduced the number of glia. Cotransfection of rax with reporter constructs containing the Hes1 or notch1 regulatory regions led to the upregulation of reporter transcription. These data suggest a regulatory heirarchy that controls the formation of glia at the expense of neurons.Neuron 06/2000; 26(2):383-94. · 14.74 Impact Factor -
Article: Diverse mechanisms regulate stem cell self-renewal.
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ABSTRACT: To what extent are the pathways that regulate self-renewal conserved between stem cells at different stages of development and in different tissues? Some pathways play a strikingly conserved role in regulating the self-renewal of diverse stem cells, whereas other pathways are specific to stem cells in certain tissues or at certain stages of development. Recent studies have highlighted differences between the self-renewal of embryonic, fetal and adult stem cells. By understanding these similarities and differences we may come to a molecular understanding of how stem cells replicate themselves and why aspects of this process differ between stem cells.Current Opinion in Cell Biology 01/2005; 16(6):700-7. · 12.90 Impact Factor -
Article: Control of epidermal stem cell clusters by Notch-mediated lateral induction.
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ABSTRACT: Stem cells in the basal layer of human interfollicular epidermis form clusters that can be reconstituted in vitro. In order to supply the interfollicular epidermis with differentiated cells, the size of these clusters must be controlled. Evidence suggests that control is regulated via differentiation of stem cells on the periphery of the clusters. Moreover, there is growing evidence that this regulation is mediated by the Notch signalling pathway. In this paper, we develop theoretical arguments, in conjunction with computer simulations of a model of the basal layer, to show that regulation of differentiation is the most likely mechanism for cluster control. In addition, we show that stem cells must adhere more strongly to each other than they do to differentiated cells. Developing our model further we show that lateral-induction, mediated by the Notch signalling pathway, is a natural mechanism for cluster control. It can not only indicate to cells the size of the cluster they are in and their position within it, but it can also control the cluster size. This can only be achieved by postulating a secondary, cluster wide, differentiation signal, and cells with high Delta expression being deaf to this signal.Developmental Biology 07/2003; 258(1):141-53. · 4.07 Impact Factor
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Keywords
apparent increase
broad bands
cell proliferation
dorsal neural tube
gain-of-function analysis
increases
migratory stream
modulating Notch/Delta signaling
nervous system formation
neural
neural tube
neural tube increases
neurons
potential function
precursors
prominent
retrovirally-mediated gene transfer
trunk neural
upregulates Delta-1 expression