成骨细胞
泛素连接酶
细胞生物学
泛素
转录因子
信号转导
蛋白酶体
生物
化学
生物化学
基因
体外
作者
Jianlin Shen,Bowen Fu,Yanfang Li,Yanjiao Wu,Hongxun Sang,Heshi Zhang,Haibin Lin,Huan Liu,Wenhua Huang
标识
DOI:10.3389/fcell.2021.706395
摘要
The ubiquitin–proteasome system (UPS) is an essential pathway that regulates the homeostasis and function of intracellular proteins and is a crucial protein-degradation system in osteoblast differentiation and bone formation. Abnormal regulation of ubiquitination leads to osteoblast differentiation disorders, interfering with bone formation and ultimately leading to osteoporosis. E3 ubiquitin ligases (E3) promote addition of a ubiquitin moiety to substrate proteins, specifically recognizing the substrate and modulating tyrosine kinase receptors, signaling proteins, and transcription factors involved in the regulation of osteoblast proliferation, differentiation, survival, and bone formation. In this review, we summarize current progress in the understanding of the function and regulatory effects of E3 ligases on the transcription factors and signaling pathways that regulate osteoblast differentiation and bone formation. A deep understanding of E3 ligase-mediated regulation of osteoblast differentiation provides a scientific rationale for the discovery and development of novel E3-targeting therapeutic strategies for osteoporosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI