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Endocrinology, doi:10.1210/en.2002-221057
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Endocrinology Vol. 144, No. 8 3524-3531
Copyright © 2003 by The Endocrine Society

Interleukin-7 Is a Direct Inhibitor of in Vitro Osteoclastogenesis

Sun-Kyeong Lee, Judith F. Kalinowski, Sandra L. Jastrzebski, Lynn Puddington and Joseph A. Lorenzo

Division of Endocrinology (S.-K.L., J.F.K., S.L.J., J.A.L.) and Division of Immunology (L.P.), Department of Medicine, The University of Connecticut Health Center, Farmington, Connecticut 06030

Address all correspondence and requests for reprints to: Dr. Sun-Kyeong Lee, Division of Endocrinology, Department of Medicine, MC-1850, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, Connecticut 06030-1850. E-mail: slee{at}neuron.uchc.edu.

We examined the direct effects of IL-7 on osteoclastogenesis in murine bone marrow cultures, using cells from wild-type and IL-7- and IL-7 receptor (IL-7R)-deficient mice. IL-7 inhibited osteoclast-like cells (OCL) formation in macrophage colony-stimulating factor (M-CSF) and receptor activator of nuclear factor {kappa}B ligand (RANKL)-stimulated (both at 30 ng/ml) murine bone marrow cultures. Significant inhibitory effects were seen at 1 ng/ml (57%) and 10 ng/ml (86%). IL-7 also inhibited (P < 0.05) OCL formation in bone marrow cultures that were stimulated with vitamin D3 (10-8 M, 60%), bovine PTH (bPTH) (100 ng/ml, 54%), or RANKL alone (30 ng/ml, 50%). IL-7 (10 ng/ml) increased expression of the B lymphocyte marker B220 from 40–86% of total nonadherent cells in cultures treated with M-CSF and RANKL. Bone marrow cells from IL-7-deficient [IL-7 knockout (KO)] mice showed a significant (P < 0.05) increase in tartrate-resistant acid phosphatase(+) OCL numbers in cultures that were stimulated with vitamin D3 (136 ± 13.3%), bPTH (196 ± 18.8%), or M-CSF and RANKL (160 ± 7.2%). In contrast, in vitro osteoclast formation in bone marrow from IL-7R-deficient (IL-7R KO) mice showed a significant decrease in tartrate-resistant acid phosphatase(+) OCL numbers in cultures that were stimulated with vitamin D3, PTH, RANKL, or M-CSF and RANKL. These results demonstrate that there are differences in the mechanisms regulating OCL formation between IL-7 KO and IL-7R KO cells. It seems that IL-7 is a direct inhibitor of OCL formation in vitro, based on results of adding IL-7 to wild-type cultures and the responses of IL-7 KO cells. It is unknown why IL-7R KO cells behave differently from IL-7 KO cells in vitro. However, it is possible that additional cytokines interact with IL-7R and that loss of these signals contributes to the responses of IL-7R KO cells. Alternatively, IL-7 may interact with multiple receptors.




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