Effects of human recombinant CSF‐GM and highly purified CSF‐1 on the formation of multinucleated cells with osteoclast characteristics in long‐term bone marrow cultures

Several studies have suggested that the osteoclast is derived from a mononuclear precursor which is found in bone marrow. We have developed a system for studying the formation of osteoclast‐like multinucleated cells in long‐term bone marrow culture of baboon cells. Recombinant human CSF‐GM and highl...

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Published in:Journal of bone and mineral research Vol. 1; no. 2; pp. 227 - 233
Main Authors: MacDonald, B. R., Mundy, G. R., Clark, S., Wang, E. A., Kuehl, T. J., Stanley, E. R., Roodman, G. D.
Format: Journal Article
Language:English
Published: Washington, DC John Wiley and Sons and The American Society for Bone and Mineral Research (ASBMR) 01-04-1986
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Summary:Several studies have suggested that the osteoclast is derived from a mononuclear precursor which is found in bone marrow. We have developed a system for studying the formation of osteoclast‐like multinucleated cells in long‐term bone marrow culture of baboon cells. Recombinant human CSF‐GM and highly purified CSF‐1, both of which stimulate the proliferation of monocyte/macrophage precursors, were found to increase the number of osteoclast‐like cells formed in long‐term bone marrow culture. CSF‐GM stimulated multinucleated cell formation more consistently than CSF‐1. The subsequent addition of 1,25‐dihydroxyvitamin D3 (1,25‐(OH)2D3) to cultures initially treated with CSF‐GM or CSF‐1 further increased multinucleated cell formation. Autoradiographic studies indicate that CSF stimulated multinucleated cell formation by increasing the proliferation of the precursor cell, and that the potentiating effect of 1,25‐(OH)2D3 was caused by fusion of the increased numbers of precursors. These studies suggest that the interaction of locally produced colony‐stimulating factors with circulating calcium regulating hormones may be important in the control of osteoclast formation and bone resorption.
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ISSN:0884-0431
1523-4681
DOI:10.1002/jbmr.5650010210