骨免疫学
骨质疏松症
兰克尔
免疫系统
骨吸收
串扰
免疫学
破骨细胞
医学
骨重建
内科学
物理
激活剂(遗传学)
光学
受体
作者
Fei Huang,Puiian Wong,Jinglan Li,Zheng Lv,Liangliang Xu,Genfu Zhu,Mincong He,Yiwen Luo
摘要
Abstract Osteoporosis is a bone disease that is caused by disorder of the skeletal microenvironment, and it characterized by a high disability rate and the occurrence of low energy fractures. Studies on osteoporosis and related treatment options have always been hot spots in the field of bone biology. In the past, the understanding of osteoporosis has been rather limited; research has only shown that osteoporosis involves the imbalance of bone resorption and bone formation, and recent studies have not provided cutting‐edge theories of the basic understanding of osteoporosis. Recent studies have shown crosstalk between bone and immune responses. RANKL, an essential factor for osteoclasts (OCs), is associated with the immune system. T helper (Th17)/regulatory T (Treg) cells are two different kinds of T cells that can self‐interact and regulate the differentiation and formation of OCs. Therefore, understanding the correlation between the skeletal and immune systems and further revealing the roles and the cooperation between RANKL and the Th17/Treg balance will help to provide new insights for the treatment of osteoporosis.
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