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The role of Notch signaling pathway in metabolic bone diseases
被引:16
作者:
Gao, Yongguang
[1
]
Fu, Zhanda
[1
]
Guan, Junxia
[1
]
Liu, Xinhua
[1
]
Zhang, Qing
[1
]
机构:
[1] Tangshan Normal Univ, Dept Chem, Tangshan Key Lab Green Special Chem, Tangshan 063000, Peoples R China
关键词:
Metabolic bone diseases;
Notch signaling pathway;
Spondylocostal dysostosis;
Osteoblast;
Osteoclast;
Notch receptor;
CAUSES SPONDYLOCOSTAL DYSOSTOSIS;
ABNORMAL VERTEBRAL SEGMENTATION;
NEGATIVE REGULATORY REGION;
MESENCHYMAL STEM-CELLS;
ALAGILLE-SYNDROME;
OSTEOGENIC DIFFERENTIATION;
CONGENITAL SCOLIOSIS;
DELTA HOMOLOG;
TBX6;
CAUSES;
MUTATIONS;
D O I:
10.1016/j.bcp.2022.115377
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Metabolic bone diseases is the third most common endocrine diseases after diabetes and thyroid diseases. More than 500 million people worldwide suffer from metabolic bone diseases. The generation and development of bone metabolic diseases is a complex process regulated by multiple signaling pathways, among which the Notch signaling pathway is one of the most important pathways. The Notch signaling pathway regulates the differ-entiation and function of osteoblasts and osteoclasts, and affects the process of cartilage formation, bone for-mation and bone resorption. Genetic mutations in upstream and downstream of Notch signaling genes can lead to a series of metabolic bone diseases, such as Alagille syndrome, Adams-Oliver syndrome and spondylocostal dysostosis. In this review, we analyzed the mechanisms of Notch ligands, Notch receptors and signaling mole-cules in the process of signal transduction, and summarized the progress on the pathogenesis and clinical manifestations of bone metabolic diseases caused by Notch gene mutation. We hope to draw attention to the role of the Notch signaling pathway in metabolic bone diseases and provide new ideas and approaches for the diagnosis and treatment of metabolic bone diseases.
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页数:12
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