A role for cell-surface CSF-1 in osteoblast-mediated osteoclastogenesis

被引:35
作者
Yao, GQ
Sun, BH
Weir, EC
Insogna, KL
机构
[1] Univ Edinburgh, Edinburgh, Midlothian, Scotland
[2] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06520 USA
关键词
cell surface; CSF-1; osteoclastogenesis; co-culture;
D O I
10.1007/s00223-001-1079-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CSF-1 is required for osteoblast-mediated osteoclast formation. Osteoblasts produce soluble (sCSF-1) and cell-surface forms of CSF-1 (also known as membrane-bound CSF-1, mCSF-1) but their individual contributions to osteoclastogenesis remain unclear. Using glutaraldehyde-fixed primary murine osteoblasts as a source of mCSF-1, osteoblasts from op/ op mice as a source for other osteoblast-derived osteoclastogenic factors and murine bone marrow as a source of osteoclast progenitors, osteoclast-like cells (OCL) formation was observed after 7-9 days of co-culture. In contrast, no OCL formation occurred when mCSF-1 expressed by primary murine osteoblasts was blocked by CSF-1 antibody pretreatment or when op/op osteoblasts were substituted for primary murine osteoblasts in the co-culture system. Osteoclast formation was also significantly inhibited when murine primary osteoblasts were pretreated with an antisense phosphorothioate oligonucleotide against mCSF-1. Finally, mCSF-1 and sCSF-1 were synergistic in stimulating OCL formation. These data support the conclusion that mCSF-1 plays an important role in osteoblast-mediated osteoclastogenesis within the bone microenvironment.
引用
收藏
页码:339 / 346
页数:8
相关论文
共 40 条
[1]  
Baron R., 1983, BONE HISTOMORPHOMETR
[2]   M-CSF neutralization and Egr-1 deficiency prevent ovariectomy-induced bone loss [J].
Cenci, S ;
Weitzmann, MN ;
Gentile, MA ;
Aisa, MC ;
Pacifici, R .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (09) :1279-1287
[3]   HUMAN MACROPHAGE-COLONY STIMULATING FACTOR - ALTERNATIVE RNA AND PROTEIN PROCESSING FROM A SINGLE GENE [J].
CERRETTI, DP ;
WIGNALL, J ;
ANDERSON, D ;
TUSHINSKI, RJ ;
GALLIS, BM ;
STYA, M ;
GILLIS, S ;
URDAL, DL ;
COSMAN, D .
MOLECULAR IMMUNOLOGY, 1988, 25 (08) :761-770
[4]   Increasing membrane-bound MCSF does not enhance OPGL-driven osteoclastogenesis from marrow cells [J].
Fan, X ;
Fan, D ;
Gewant, H ;
Royce, CL ;
Nanes, MS ;
Rubin, J .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2001, 280 (01) :E103-E111
[5]   MACROPHAGE-COLONY-STIMULATING FACTOR STIMULATES SURVIVAL AND CHEMOTACTIC BEHAVIOR IN ISOLATED OSTEOCLASTS [J].
FULLER, K ;
OWENS, JM ;
JAGGER, CJ ;
WILSON, A ;
MOSS, R ;
CHAMBERS, TJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (05) :1733-1744
[6]   MACROPHAGE COLONY STIMULATING FACTOR (M-CSF) IS ESSENTIAL FOR OSTEOCLAST FORMATION INVITRO [J].
HATTERSLEY, G ;
OWENS, J ;
FLANAGAN, AM ;
CHAMBERS, TJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 177 (01) :526-531
[7]   Importance of membrane- or matrix-associated forms of M-CSF and RANKL/ODF in osteoclastogenesis supported by SaOS-4/3 cells expressing recombinant PTH/PTHrP receptors [J].
Itoh, K ;
Udagawa, N ;
Matsuzaki, K ;
Takami, M ;
Amano, H ;
Shinki, T ;
Ueno, Y ;
Takahashi, N ;
Suda, T .
JOURNAL OF BONE AND MINERAL RESEARCH, 2000, 15 (09) :1766-1775
[8]   MACROPHAGE-COLONY-STIMULATING FACTOR AND INTERLEUKIN-1A MAINTAIN THE SURVIVAL OF OSTEOCLAST-LIKE CELLS [J].
JIMI, E ;
SHUTO, T ;
KOGA, T .
ENDOCRINOLOGY, 1995, 136 (02) :808-811
[9]   MOLECULAR-CLONING OF A COMPLEMENTARY-DNA ENCODING HUMAN MACROPHAGE-SPECIFIC COLONY-STIMULATING FACTOR (CSF-1) [J].
KAWASAKI, ES ;
LADNER, MB ;
WANG, AM ;
VANARSDELL, J ;
WARREN, MK ;
COYNE, MY ;
SCHWEICKART, VL ;
LEE, MT ;
WILSON, KJ ;
BOOSMAN, A ;
STANLEY, ER ;
RALPH, P ;
MARK, DF .
SCIENCE, 1985, 230 (4723) :291-296
[10]   Estrogen deficiency increases the ability of stromal cells to support murine osteoclastogenesis via an interleukin-1- and tumor necrosis factor-mediated stimulation of macrophage colony-stimulating factor production [J].
Kimble, RB ;
Srivastava, S ;
Ross, FP ;
Matayoshi, A ;
Pacifici, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (46) :28890-28897