成骨细胞
细胞生物学
旁分泌信号
骨重建
血管生成
破骨细胞
化学
并列信号
骨吸收
骨免疫学
生物
内分泌学
癌症研究
生物化学
体外
激活剂(遗传学)
基因
受体
兰克尔
作者
Sipin Zhu,Felix Yao,Heng Qiu,Ge Zhang,Huazi Xu,Jiake Xu
摘要
ABSTRACT Bone remodelling is a continuous process by which bone resorption by osteoclasts is followed by bone formation by osteoblasts to maintain skeletal homeostasis. These two forces must be tightly coordinated not only quantitatively, but also in time and space, and its malfunction leads to diseases such as osteoporosis. Recent research focusing on the cross‐talk and coupling mechanisms associated with the sequential recruitment of osteoblasts to areas where osteoclasts have removed bone matrix have identified a number of osteogenic factors produced by the osteoclasts themselves. Osteoclast‐derived factors and exosomal‐containing micro RNA (mi RNA ) can either enhance or inhibit osteoblast differentiation through paracrine and juxtacrine mechanisms, and therefore may have a central coupling role in bone formation. Entwined with angiocrine factors released by vessel‐specific endothelial cells and perivascular cells or pericytes, these factors play a critical role in angiogenesis–osteogenesis coupling essential in bone remodelling.
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