Clonal endothelial cells produce humoral factors that inhibit osteoclast-like cell formation in vitro

被引:18
作者
Chikatsu, N
Takeuchi, Y
Fukumoto, S
Yano, K
Fujita, N
Tsuruo, T
Fujita, T
机构
[1] Univ Tokyo, Sch Med, Dept Med, Div Endocrinol,Bunkyo Ku, Tokyo 1138655, Japan
[2] Univ Tokyo, Sch Med, Dept Lab Med, Tokyo 1138655, Japan
[3] Snow Brand Milk Prod Co Ltd, Life Sci Res Inst, Ishibashi, Tochigi 3290512, Japan
[4] Univ Tokyo, Inst Mol & Cellular Biosci, Tokyo 1130032, Japan
关键词
endothelial cell; bone marrow cell; osteoclast; RANKL; osteoprotegerin;
D O I
10.1507/endocrj.49.439
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Angiogenesis and bone remodeling are closely associated, and vascular endothelial cells may have potential roles for osteoclastic bone resorption. We examined whether clonal endothelial cells established from bone, aorta and brain of Balb/c mice influenced osteoclast-like cell formation in vitro. As low as 1% conditioned media of those endothelial cells inhibited osteoclast-like cell formation in bone marrow cultures induced by 1,25-dihydroxyvitamin D-3, and did so in spleen cell cultures in the presence of soluble receptor activator of nuclear factor-kappaB ligand (RANKL), M-CSF and prostaglandin E-2. The level of osteoprotegerin (OPG), a decoy receptor for RANKL, secreted by endothelial cells was not high enough to inhibit osteoclastogenesis. These observations suggest that endothelial cells derived from various tissues secrete factor(s) that inhibits precursors to differentiate into osteoclasts even in the presence of optimal stimulators for osteoclastogenesis. Hence, endothelial cells in bone may inhibit recruitment of fresh osteoclasts, and those in tissues other than bone may be involved in prohibiting ectopic osteoclastogenesis.
引用
收藏
页码:439 / 447
页数:9
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