The osteocyte plays multiple roles in bone remodeling and mineral homeostasis

被引:121
作者
Chen, Huayue [1 ]
Senda, Takao [1 ]
Kubo, Kin-ya [2 ]
机构
[1] Gifu Univ, Grad Sch Med, Dept Anat, Gifu 5011194, Japan
[2] Seijoh Univ, Grad Sch Hlth Care Studies, Tokai, Aichi 4768588, Japan
关键词
Osteocyte; Lacunar-canalicular system; Sclerostin; FGF23; RANKL; Osteoporosis; FIBROBLAST-GROWTH-FACTOR; PARATHYROID-HORMONE; POSTMENOPAUSAL OSTEOPOROSIS; OSTEOBLAST PROGENITORS; SENILE OSTEOPOROSIS; CELL PROCESSES; MURINE MODEL; IN-VIVO; SCLEROSTIN; APOPTOSIS;
D O I
10.1007/s00795-015-0099-y
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
Osteocytes are the most abundant cells in bone and are the major orchestrators of bone remodeling and mineral homeostasis. They possess a specialized cellular morphology and a unique molecular feature. Osteocytes are a stellate shape with numerous long, slender dendritic processes. The osteocyte cell body resides in the bone matrix of the lacuna and the dendritic processes extend within the canaliculi to adjacent osteocytes and other cells on the bone surface. Osteocytes form extensive intercellular network to sense and respond to environmental mechanical stimulus by the lacunar-canalicular system and gap junction. Osteocytes are long-lived bone cells. They can undergo apoptosis, which may have specific regulatory effects on osteoclastic bone resorption. Osteocytes can secrete several molecules, including sclerostin, receptor activator of nuclear factor kappa B ligand and fibroblast growth factor 23 to regulate osteoblastic bone formation, osteoclastic bone resorption and mineral homeostasis. A deeper understanding of the complex mechanisms that mediate the control of osteoblast and osteoclast function by osteocytes may identify new osteocyte-derived molecules as potential pharmacological targets for treating osteoporosis and other skeletal diseases.
引用
收藏
页码:61 / 68
页数:8
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