Effect of Estrogen on the Activity and Growth of Human Osteoclasts In Vitro
Accepted 8 December 2008.
Summary
Objective
Estrogen deficiency results in postmenopausal osteoporosis by increasing the rate of bone loss. The mechanism responsible for the effects of estrogen on osteoclasts is still unclear.
Materials and Methods
The potential of mononuclear cells from cord blood or bone marrow to differentiate into mature osteoclasts when co-cultured with human osteoblast cells was investigated. The effects of estrogen on osteoclastogenesis and osteoclast activity were also examined.
Results
Macrophage markers CD11b and CD14 were downregulated and vitronectin receptor was upregulated during 28 days' co-culture of mononuclear cells and human osteoblasts. Long-term co-culture resulted in the formation of numerous large tartrate-resistant acid phosphatase-positive multinucleated cells capable of resorption of bone slices. After incubation for 28 days, the addition of 17β-estradiol caused a significant decrease in the expression of vitronectin receptor and tartrate-resistant acid phosphatase-positive multinucleated cells in cultures derived from both bone marrow and cord blood. A significant decrease in bone resorption was also noted in the presence of estrogen.
Conclusion
Estrogen not only suppresses osteoclastogenesis but also inhibits the activity of osteoclasts.
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aDepartment Orthopedic Surgery, Keelung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine, National Taiwan Ocean University, Keelung, Taiwan
bInstitute of Marine Biology, National Taiwan Ocean University, Keelung, Taiwan
cDepartment of Obstetrics and Gynecology, National Taiwan Ocean University, Keelung, Taiwan
Correspondence to: Dr Fang-Ping Chen, Department Of Obstetrics and Gynecology, Keelung Chang Gung Memorial Hospital, 222, Mai-Chin Road, Keelung, Taiwan