NOTCH SIGNALING IN DEVELOPMENT, TISSUE HOMEOSTASIS, AND DISEASE

被引:796
作者
Siebel, Chris
Lendahl, Urban [1 ]
机构
[1] Karolinska Inst, Dept Cell & Mol Biol, SE-17177 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
SMOOTH-MUSCLE-CELLS; GAMMA-SECRETASE INHIBITORS; NEURAL STEM-CELLS; EPITHELIAL-MESENCHYMAL TRANSITION; AUTOSOMAL-DOMINANT ARTERIOPATHY; BILE-DUCT DEVELOPMENT; HAJDU-CHENEY-SYNDROME; CAUSES SPONDYLOCOSTAL DYSOSTOSIS; PULMONARY ARTERIAL-HYPERTENSION; ACUTE LYMPHOBLASTIC-LEUKEMIA;
D O I
10.1152/physrev.00005.2017
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Notch signaling is an evolutionarily highly conserved signaling mechanism, but in contrast to signaling pathways such as Wnt, Sonic Hedgehog, and BMP/TGF-beta, Notch signaling occurs via cell-cell communication, where transmembrane ligands on one cell activate transmembrane receptors on a juxtaposed cell. Originally discovered through mutations in Drosophila more than 100 yr ago, and with the first Notch gene cloned more than 30 yr ago, we are still gaining new insights into the broad effects of Notch signaling in organisms across the metazoan spectrum and its requirement for normal development of most organs in the body. In this review, we provide an overview of the Notch signaling mechanism at the molecular level and discuss how the pathway, which is architecturally quite simple, is able to engage in the control of cell fates in a broad variety of cell types. We discuss the current understanding of how Notch signaling can become derailed, either by direct mutations or by aberrant regulation, and the expanding spectrum of diseases and cancers that is a consequence of Notch dysregulation. Finally, we explore the emerging field of Notch in the control of tissue homeostasis, with examples from skin, liver, lung, intestine, and the vasculature.
引用
收藏
页码:1235 / 1294
页数:60
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