Tumor necrosis factor-α induces differentiation of and bone resorption by osteoclasts

被引:611
作者
Azuma, Y
Kaji, K
Katogi, R
Takeshita, S
Kudo, A
机构
[1] Tokyo Inst Technol, Dept Life Sci, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[2] Teijin Ltd, Teijin Inst Biomed Res, Hino, Tokyo 1918512, Japan
关键词
D O I
10.1074/jbc.275.7.4858
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Osteoclast progenitors differentiate into mature osteoclasts in the presence of receptor activator of NF-KB (RANK) ligand on stromal or osteoblastic cells and monocyte macrophage colony-stimulating factor (M-CSF), The soluble RANK ligand induces the same differentiation in vitro without stromal cells, Tumor necrosis factor-alpha (TNF-alpha), a potent cytokine involved in the regulation of osteoclast activity, promotes bone resorption via a primary effect on osteoblasts; however, it remains unclear whether TNF-alpha can also directly induce the differentiation of osteoclast progenitors into mature osteoclasts, This study revealed that TNF-alpha directly induced the formation of tartrate-resistant acid phosphatase (TRAP)-positive multinucleated cells (MNCs), which produced resorption pits on bone in vitro in the presence of M-CSF, The bone resorption activity of TNF-alpha-induced MNCs was lower than that of soluble RANK ligand-induced MNCs; however, interleukin-lp stimulated this activity of TNF cu-induced MNCs without an increase in the number of MNCs, In this case, interleukin-lp did not induce TRAP-positive MNC formation. The osteoclast progenitors expressed TNF receptors, p55 and p75; and the induction of TRAP-positive MNCs by TNF-alpha was inhibited completely by an anti-p55 antibody and partially by an anti-p75 antibody. Our findings presented here are the first to indicate that TNF-alpha is a crucial differentiation factor for osteoclasts. Our results suggest that TNF-alpha and M-CSF play an important role in local osteolysis in chronic inflammatory diseases.
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收藏
页码:4858 / 4864
页数:7
相关论文
共 58 条
[1]
Lipopolysaccharide-stimulated osteoclastogenesis is mediated by tumor necrosis factor via its P55 receptor [J].
AbuAmer, Y ;
Ross, FP ;
Edwards, J ;
Teitelbaum, SL .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (06) :1557-1565
[2]
Apoptosis control by death and decoy receptors [J].
Ashkenazi, A ;
Dixit, VM .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (02) :255-260
[3]
STIMULATION OF BONE-RESORPTION AND INHIBITION OF BONE-FORMATION INVITRO BY HUMAN-TUMOR NECROSIS FACTORS [J].
BERTOLINI, DR ;
NEDWIN, GE ;
BRINGMAN, TS ;
SMITH, DD ;
MUNDY, GR .
NATURE, 1986, 319 (6053) :516-518
[4]
Boyce BF, 1999, LAB INVEST, V79, P83
[5]
INVITRO FORMATION OF OSTEOCLASTS FROM LONG-TERM CULTURES OF BONE-MARROW MONONUCLEAR PHAGOCYTES [J].
BURGER, EH ;
VANDERMEER, JWM ;
VANDEGEVEL, JS ;
GRIBNAU, JC ;
THESINGH, CW ;
VANFURTH, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 156 (06) :1604-1614
[6]
PRODUCTION OF VARIOUS CYTOKINES BY NORMAL HUMAN OSTEOBLAST-LIKE CELLS IN RESPONSE TO INTERLEUKIN-1-BETA AND TUMOR-NECROSIS-FACTOR-ALPHA - LACK OF REGULATION BY 17-BETA-ESTRADIOL [J].
CHAUDHARY, LR ;
SPELSBERG, TC ;
RIGGS, BL .
ENDOCRINOLOGY, 1992, 130 (05) :2528-2534
[7]
DAVIES JE, 1993, CELL MATER, V3, P245
[8]
THE INTERLEUKIN-1 FAMILY - 10 YEARS OF DISCOVERY [J].
DINARELLO, CA .
FASEB JOURNAL, 1994, 8 (15) :1314-1325
[9]
MURINE OSTEOBLAST-LIKE CELLS AND THE OSTEOGENIC CELL MC3T3-E1 RELEASE A MACROPHAGE COLONY-STIMULATING ACTIVITY IN CULTURE [J].
ELFORD, PR ;
FELIX, R ;
CECCHINI, M ;
TRECHSEL, U ;
FLEISCH, H .
CALCIFIED TISSUE INTERNATIONAL, 1987, 41 (03) :151-156
[10]
FAHLMAN C, 1994, BLOOD, V84, P1528