Notch signaling in the mammalian respiratory system, specifically the trachea and lungs, in development, homeostasis, regeneration, and disease

被引:93
作者
Kiyokawa, Hirofumi [1 ]
Morimoto, Mitsuru [1 ]
机构
[1] RIKEN, Ctr Biosyst Dynam Res, Lab Lung Dev & Regenerat, Kobe, Hyogo 6500047, Japan
基金
日本学术振兴会;
关键词
human disease; lung development; mouse genetics; Notch signaling; organogenesis; NEUROEPITHELIAL BODY MICROENVIRONMENT; PULMONARY NEUROENDOCRINE CELLS; BASAL-CELLS; AIRWAY EPITHELIUM; PRESENILIN; STEM-CELLS; DIFFERENTIATION; PATHWAY; CLARA; PROMOTES;
D O I
10.1111/dgd.12628
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The respiratory system has ideal tissue structure and cell types for efficient gas exchange to intake oxygen and release carbon dioxide. This complex system develops through orchestrated intercellular signaling among various cell types, such as club, ciliated, basal, neuroendocrine, AT1, AT2, endothelial, and smooth muscle cells. Notch signaling is a highly conserved cell-cell signaling pathway ideally suited for very short-range cellular communication because Notch signals are transmitted by direct contact with an adjacent cell. Enthusiastic efforts by Notch researchers over the last two decades have led to the identification of critical roles of this signaling pathway during development, homeostasis, and regeneration of the respiratory system. The dysregulation of Notch signaling results in a wide range of respiratory diseases such as pulmonary artery hypertension (PAH), chronic obstructive pulmonary disease (COPD), interstitial pulmonary fibrosis (IPF), and lung cancer. Thus, a deep understanding of the biological functions of Notch signaling will help identify novel treatment targets in various respiratory diseases.
引用
收藏
页码:67 / 79
页数:13
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