Cell cycle arrest and apoptosis induced by Notch1 in B cells

被引:125
作者
Morimura, T
Goitsuka, R
Zhang, Y
Saito, I
Reth, M
Kitamura, D [1 ]
机构
[1] Tokyo Univ Sci, Biosci Res Inst, Div Mol Biol, Noda, Chiba 2780022, Japan
[2] Japan Sci & Technol Corp, PRESTO, Noda, Chiba 2780022, Japan
[3] Univ Freiburg, Dept Mol Immunol, D-79108 Freiburg, Germany
[4] Max Planck Inst Immunobiol, D-79108 Freiburg, Germany
[5] Univ Tokyo, Inst Med Sci, Genet Mol Lab, Minato Ku, Tokyo 1088639, Japan
关键词
D O I
10.1074/jbc.M006415200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Notch receptors play various roles for cell fate decisions in developing organs, although their functions at the cell level are poorly understood. Recently, we found that Notch1 and its ligand are each expressed in juxta-posed cell compartments in the follicles of the bursa of Fabricius, the central organ for chicken B cell development. To examine the function of Notch1 in B cells, a constitutively active form of chicken Notch1 was expressed in a chicken B cell line, DT40, by a Cre/loxP-mediated inducible expression system. Remarkably, the active Notch1 caused growth suppression of the cells, accompanied by a cell cycle inhibition at the G(1) phase and apoptosis. The expression of Hairy1, a gene product up-regulated by the Notch1 signaling, also induced the apoptosis, but no cell cycle inhibition. Thus, Notch1 signaling induces apoptosis of the B cells through Hairy1, and the G(1) cell cycle arrest through other pathways. This novel function of Notch1 may account for the recent observations indicating the selective inhibition of early B cell development in mice by Notch1.
引用
收藏
页码:36523 / 36531
页数:9
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