Endocytic regulation of Notch signaling

被引:142
作者
Fortini, Mark E. [1 ]
Bilder, David [2 ]
机构
[1] Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
SPECIFY CELL FATE; GENE BIG BRAIN; MEMBRANE LOCALIZATION; DROSOPHILA; ACTIVATION; TRAFFICKING; RECEPTOR; PROTEIN; SUPPRESSOR; DELTA;
D O I
10.1016/j.gde.2009.04.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Endocytosis and endosomal trafficking have emerged as important cell biological steps in the Notch developmental signaling pathway. Ligand endocytosis helps generate the physical forces needed to dissociate and activate the receptor, and activated receptors enter endosomes to signal productively. Endosomal trafficking is also responsible for downregulating Notch receptors that have not been activated by ligand. Recent studies have provided new insights into these Notch trafficking steps, and have uncovered additional endosomal mechanisms that contribute to asymmetric Notch activation and ligand-independent Notch signaling.
引用
收藏
页码:323 / 328
页数:6
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