Genetic regulation of osteoclast development and function

被引:1285
作者
Teitelbaum, SL [1 ]
Ross, FP [1 ]
机构
[1] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA
关键词
D O I
10.1038/nrg1122
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Osteoclasts are the principal, if not exclusive, bone-resorbing cells, and their activity has a profound impact on skeletal health. So, disorders of skeletal insufficiency, such as osteoporosis, typically represent enhanced osteoclastic bone resorption relative to bone formation. Prevention of pathological bone loss therefore depends on an appreciation of the mechanisms by which osteoclasts differentiate from their precursors and degrade the skeleton. The past five years have witnessed important insights into osteoclast formation and function. Many of these discoveries have been made through genetic experiments that involved the rare hereditary disorder osteopetrosis.
引用
收藏
页码:638 / 649
页数:12
相关论文
共 126 条
[51]   Osteoclasts are present in gp130-deficient mice [J].
Kawasaki, K ;
Gao, YH ;
Yokose, S ;
Kaji, Y ;
Nakamura, T ;
Suda, T ;
Yoshida, K ;
Taga, T ;
Kishimoto, T ;
Kataoka, H ;
Yuasa, T ;
Norimatsu, H ;
Yamaguchi, A .
ENDOCRINOLOGY, 1997, 138 (11) :4959-4965
[52]   Clinical review 144 - Estrogen and the male skeleton [J].
Khosla, S ;
Melton, LJ ;
Riggs, BL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (04) :1443-1450
[53]   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
[54]   OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis [J].
Kong, YY ;
Yoshida, H ;
Sarosi, I ;
Tan, HL ;
Timms, E ;
Capparelli, C ;
Morony, S ;
Oliveira-dos-Santos, AJ ;
Van, G ;
Itie, A ;
Khoo, W ;
Wakeham, A ;
Dunstan, CR ;
Lacey, DL ;
Mak, TW ;
Boyle, WJ ;
Penninger, JM .
NATURE, 1999, 397 (6717) :315-323
[55]   Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis [J].
Kornak, U ;
Schulz, A ;
Friedrich, W ;
Uhlhaas, S ;
Kremens, B ;
Voit, T ;
Hasan, C ;
Bode, U ;
Jentsch, TJ ;
Kubisch, C .
HUMAN MOLECULAR GENETICS, 2000, 9 (13) :2059-2063
[56]   Loss of the CIC-7 chloride channel leads to osteopetrosis in mice and man [J].
Kornak, U ;
Kasper, D ;
Bösl, MR ;
Kaiser, E ;
Schweizer, M ;
Schulz, A ;
Friedrich, W ;
Delling, G ;
Jentsch, TJ .
CELL, 2001, 104 (02) :205-215
[57]   Osteoprotegerin ligand is a cytokine that regulates osteoclast differentiation and activation [J].
Lacey, DL ;
Timms, E ;
Tan, HL ;
Kelley, MJ ;
Dunstan, CR ;
Burgess, T ;
Elliott, R ;
Colombero, A ;
Elliott, G ;
Scully, S ;
Hsu, H ;
Sullivan, J ;
Hawkins, N ;
Davy, E ;
Capparelli, C ;
Eli, A ;
Qian, YX ;
Kaufman, S ;
Sarosi, I ;
Shalhoub, V ;
Senaldi, G ;
Guo, J ;
Delaney, J ;
Boyle, WJ .
CELL, 1998, 93 (02) :165-176
[58]   TNF-α induces osteoclastogenesis by direct stimulation of macrophages exposed to permissive levels of RANK ligand [J].
Lam, J ;
Takeshita, S ;
Barker, JE ;
Kanagawa, O ;
Ross, FP ;
Teitelbaum, SL .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 106 (12) :1481-1488
[59]   A potent small molecule, nonpeptide inhibitor of cathepsin K (SB 331750) prevents bone matrix resorption in the ovariectomized rat [J].
Lark, MW ;
Stroup, GB ;
James, IE ;
Dodds, RA ;
Hwang, SN ;
Blake, SM ;
Lechowska, BA ;
Hoffman, SJ ;
Smith, BR ;
Kapadia, R ;
Liang, X ;
Erhard, K ;
Ru, Y ;
Dong, X ;
Marquis, RW ;
Veber, D ;
Gowen, M .
BONE, 2002, 30 (05) :746-753
[60]   Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone [J].
Laurin, N ;
Brown, JP ;
Morissette, J ;
Raymond, V .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (06) :1582-1588