Notch activation induces apoptosis in neural progenitor cells through a p53-dependent pathway

被引:260
作者
Yang, XD
Klein, R
Tian, XL
Cheng, HT
Kopan, R
Shen, J
机构
[1] Harvard Univ, Sch Med, Ctr Neurol Dis, Brigham & Womens Hosp,Program Neurosci, Boston, MA 02115 USA
[2] Max Planck Inst Neurobiol, Dept Mol Neurobiol, D-82152 Martinsried, Germany
[3] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Div Dermatol, Dept Med, St Louis, MO 63110 USA
[5] Harvard Univ, Sch Med, Neurosci Program, Boston, MA 02115 USA
关键词
neural development; genetic; mouse; conditional; transgenic; knockout; Drosophila; presenilin; notch; apoptosis; p53;
D O I
10.1016/j.ydbio.2004.01.014
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Notch signaling is involved in a variety of cell-fate decisions during development. Here we investigate the role of Notch signaling in apoptotic cell death of neural progenitors through the generation and analysis of cell type-specific conditional transgenic and knockout mice. We show that conditional expression of a constitutively active form of Notch1 in early neural progenitor cells, but not postmitotic neurons, selectively induces extensive apoptosis, resulting in a markedly reduced progenitor population. Conversely, attenuation of Notch signaling in Notch1 conditional knockout or Presenilin-1-/- mice results in reduced apoptosis of early neural progenitor cells. Furthermore, Notch activation in neural progenitor cells leads to elevated levels of nuclear p53 and transcriptional upregulation of the target genes Bax and Noxa, and the promotion of apoptotic cell death by Notch activation is completely suppressed by p53 deficiency. Together, these complementary gain-of-function and loss-of-function Studies reveal a previously unappreciated role of Notch signaling in the regulation of apoptotic cell death during early mammalian neural development. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:81 / 94
页数:14
相关论文
共 83 条
[1]   HIGH-FREQUENCY DEVELOPMENTAL ABNORMALITIES IN P53-DEFICIENT MICE [J].
ARMSTRONG, JF ;
KAUFMAN, MH ;
HARRISON, DJ ;
CLARKE, AR .
CURRENT BIOLOGY, 1995, 5 (08) :931-936
[2]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[3]  
Baonza A, 2000, DEVELOPMENT, V127, P2383
[4]   A novel proteolytic cleavage involved in Notch signaling:: The role of the disintegrin-metalloprotease TACE [J].
Brou, C ;
Logeat, F ;
Gupta, N ;
Bessia, C ;
LeBail, O ;
Doedens, JR ;
Cumano, A ;
Roux, P ;
Black, RA ;
Israël, A .
MOLECULAR CELL, 2000, 5 (02) :207-216
[5]   NOTCH IS REQUIRED FOR SUCCESSIVE CELL DECISIONS IN THE DEVELOPING DROSOPHILA RETINA [J].
CAGAN, RL ;
READY, DF .
GENES & DEVELOPMENT, 1989, 3 (08) :1099-1112
[6]  
Campagne MV, 1998, J COMP NEUROL, V397, P181
[7]  
Chambers CB, 2001, DEVELOPMENT, V128, P689
[8]  
CONLON RA, 1995, DEVELOPMENT, V121, P1533
[9]  
Cornell M, 1999, GENETICS, V152, P567
[10]   A presenilin-1-dependent γ-secretase-like protease mediates release of Notch intracellular domain [J].
De Strooper, B ;
Annaert, W ;
Cupers, P ;
Saftig, P ;
Craessaerts, K ;
Mumm, JS ;
Schroeter, EH ;
Schrijvers, V ;
Wolfe, MS ;
Ray, WJ ;
Goate, A ;
Kopan, R .
NATURE, 1999, 398 (6727) :518-522