Vascular niche factor PEDF modulates Notch-dependent stemness in the adult subependymal zone

被引:170
作者
Andreu-Agullo, Celia [1 ,2 ]
Manuel Morante-Redolat, Jose [1 ,2 ]
Delgado, Ana C. [1 ,2 ]
Farinas, Isabel [1 ,2 ]
机构
[1] Univ Valencia, Dept Biol Celular, E-46100 Burjassot, Spain
[2] Univ Valencia, CIBER Enfermedades Neurodegenerat, E-46100 Burjassot, Spain
关键词
EPITHELIUM-DERIVED FACTOR; NF-KAPPA-B; AMYLOID PRECURSOR PROTEIN; NEURAL DEVELOPMENT; MAMMALIAN NOTCH; GENE-EXPRESSION; CELLS; RECEPTOR; SIGNAL; BRAIN;
D O I
10.1038/nn.2437
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
We sought to address the fundamental question of how stem cell microenvironments can regulate self-renewal. We found that Notch was active in astroglia-like neural stem cells (NSCs), but not in transit-amplifying progenitors of the murine subependymal zone, and that the level of Notch transcriptional activity correlated with self-renewal and multipotency. Moreover, dividing NSCs appeared to balance renewal with commitment via controlled segregation of Notch activity, leading to biased expression of known (Hes1) and previously unknown (Egfr) Notch target genes in daughter cells. Pigment epithelium-derived factor (PEDF) enhanced Notch-dependent transcription in cells with low Notch signaling, thereby subverting the output of an asymmetrical division to the production of two highly self-renewing cells. Mechanistically, PEDF induced a non-canonical activation of the NF-kappa B pathway, leading to the dismissal of the transcriptional co-repressor N-CoR from specific Notch-responsive promoters. Our data provide a basis for stemness regulation in vascular niches and indicate that Notch and PEDF cooperate to regulate self-renewal.
引用
收藏
页码:1514 / U57
页数:12
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共 50 条
[1]
Notch signaling is required to maintain all neural stem cell populations - Irrespective of spatial or temporal niche [J].
Alexson, TO ;
Hitoshi, S ;
Coles, BL ;
Bernstein, A ;
van der Kooy, D .
DEVELOPMENTAL NEUROSCIENCE, 2006, 28 (1-2) :34-48
[2]
Androutsellis-Theotokis A, 2006, NATURE, V442, P823, DOI 10.1038/nature04940
[3]
Notch and NFκB signaling pathways:: do they collaborate in normal vertebrate brain development and function? [J].
Ang, Hwee-Luan ;
Tergaonkar, Vinay .
BIOESSAYS, 2007, 29 (10) :1039-1047
[4]
Exchange of N-CoR corepressor and Tip60 coactivator complexes links gene expression by NF-κB and β-amyloid precursor protein [J].
Baek, SH ;
Ohgi, KA ;
Rose, DW ;
Koo, EH ;
Glass, CK ;
Rosenfeld, MG .
CELL, 2002, 110 (01) :55-67
[5]
Notch signalling: a simple pathway becomes complex [J].
Bray, Sarah J. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2006, 7 (09) :678-689
[6]
Notch regulates cell fate and dendrite morphology of newborn neurons in the postnatal dentate gyrus [J].
Breunig, Joshua J. ;
Silbereis, John ;
Vaccarino, Flora M. ;
Sestan, Nenad ;
Rakic, Pasko .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (51) :20558-20563
[7]
Pigment epithelium-derived factor inhibits angiogenesis via regulated intracellular proteolysis of vascular endothelial growth factor receptor 1 (Withdrawn Publication. See vol. 298, 2021) [J].
Cai, J ;
Jiang, WG ;
Grant, MB ;
Boulton, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (06) :3604-3613
[8]
Notch, epidermal growth factor receptor, and β1-integrin pathways are coordinated in neural stem cells [J].
Campos, LS ;
Decker, L ;
Taylor, V ;
Skarnes, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (08) :5300-5309
[9]
Forebrain ependymal cells are Notch-dependent and generate neuroblasts and astrocytes after stroke [J].
Carlen, Marie ;
Meletis, Konstantinos ;
Goritz, Christian ;
Darsalia, Vladimer ;
Evergren, Emma ;
Tanigaki, Kenji ;
Amendola, Mario ;
Barnabe-Heider, Fanie ;
Yeung, Maggie S. Y. ;
Naldini, Luigi ;
Honjo, Tasuku ;
Kokaia, Zaal ;
Shupliakov, Oleg ;
Cassidy, Robert M. ;
Lindvall, Olle ;
Frisen, Jonas .
NATURE NEUROSCIENCE, 2009, 12 (03) :259-267
[10]
Shaping the nuclear action of NF-κB [J].
Chen, LF ;
Greene, WC .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2004, 5 (05) :392-401