ENDOCYTOSIS AND INTRACELLULAR TRAFFICKING OF NOTCH AND ITS LIGANDS

被引:99
作者
Yamamoto, Shinya [1 ]
Charng, Wu-Lin [1 ]
Bellen, Hugo J. [1 ,2 ,3 ,4 ]
机构
[1] Baylor Coll Med, Program Dev Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Neurosci, Houston, TX 77030 USA
[4] Baylor Coll Med, Howard Hughes Med Inst, Houston, TX 77030 USA
来源
NOTCH SIGNALING | 2010年 / 92卷
关键词
ASYMMETRIC CELL-DIVISION; FAMILIAL ALZHEIMERS-DISEASE; GAMMA-SECRETASE ACTIVITY; LETHAL-GIANT-LARVAE; OF-DELTEX GENE; UBIQUITIN LIGASE; DROSOPHILA-MELANOGASTER; SIGNALING PATHWAY; BINDING MOTIF; MIND BOMB;
D O I
10.1016/S0070-2153(10)92005-X
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Notch signaling occurs through direct interaction between Notch, the receptor, and its ligands, presented on the surface of neighboring cells. Endocytosis has been shown to be essential for Notch signal activation in both signal-sending and signal-receiving cells, and numerous genes involved in vesicle trafficking have recently been shown to act as key regulators of the pathway. Defects in vesicle trafficking can lead to gain- or loss-of-function defects in a context-dependent manner. Here, we discuss how endocytosis and vesicle trafficking regulate Notch signaling in both signal-sending and signal-receiving cells. We will introduce the key players in different trafficking steps, and further illustrate how they impact the signal outcome. Some of these players act as general factors and modulate Notch signaling in all contexts, whereas others modulate signaling in a context-specific fashion. We also discuss Notch signaling during mechanosensory organ development in the fly to exemplify how endocytosis and vesicle trafficking are effectively used to determine correct cell fates. In summary, endocytosis plays an essential role in Notch signaling, whereas intracellular vesicle trafficking often plays a context-dependent or regulatory role, leading to divergent outcomes in different developmental contexts.
引用
收藏
页码:165 / 200
页数:36
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