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Multiple roles of ALK3 in osteoarthritis
被引:2
作者:
Ruan, X.
[1
]
Gu, J.
[1
]
Chen, M.
[1
]
Zhao, F.
[1
]
Aili, M.
[1
]
Zhang, D.
[1
]
机构:
[1] Sichuan Univ, West China Hosp Stomatol, State Key Lab Oral Dis, Chengdu, Peoples R China
来源:
BONE & JOINT RESEARCH
|
2023年
/
12卷
/
07期
基金:
中国国家自然科学基金;
中国博士后科学基金;
关键词:
ALK3;
Osteoarthritis;
Joint;
BONE MORPHOGENETIC PROTEINS;
IA RECEPTOR BMPRIA;
ARTICULAR-CARTILAGE;
SUBCHONDRAL BONE;
INDIAN HEDGEHOG;
TGF-BETA;
CHONDROCYTE DIFFERENTIATION;
UP-REGULATION;
STEM-CELLS;
OSTEOCLASTS;
D O I:
10.1302/2046-3758.127.BJR-2022-0310.R1
中图分类号:
Q813 [细胞工程];
学科分类号:
摘要:
Osteoarthritis (OA) is a chronic degenerative joint disease characterized by progressive cartilage degradation, synovial membrane inflammation, osteophyte formation, and subchondral bone sclerosis. Pathological changes in cartilage and subchondral bone are the main processes in OA. In recent decades, many studies have demonstrated that activin- like kinase 3 (ALK3), a bone morphogenetic protein receptor, is essential for cartilage formation, osteogenesis, and postnatal skeletal development. Although the role of bone morphogenetic protein (BMP) signalling in articular cartilage and bone has been extensively studied, many new discoveries have been made in recent years around ALK3 targets in articular cartilage, subchondral bone, and the interaction between the two, broadening the original knowledge of the relationship between ALK3 and OA. In this review, we focus on the roles of ALK3 in OA, including cartilage and subchondral bone and related cells. It may be helpful to seek more efficient drugs or treatments for OA based on ALK3 signalling in future.
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页码:397 / 411
页数:15
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