Osteoclast-Derived Coupling Factors in Bone Remodeling

被引:127
作者
Henriksen, Kim [1 ]
Karsdal, Morten A. [1 ]
Martin, T. John [2 ]
机构
[1] Nord Biosci Biomarkers & Res, DK-2730 Herlev, Denmark
[2] Univ Melbourne, Dept Med, St Vincents Inst Med Res, Melbourne, Vic 3065, Australia
关键词
Bone turnover; Remodeling; Osteoblast; Osteoclast; RANK; RANKL; Osteoprotegerin; MESENCHYMAL STEM-CELLS; SPHINGOSINE; 1-PHOSPHATE; EPH RECEPTORS; RESORPTION; DIFFERENTIATION; MICE; OSTEOPETROSIS; OSTEOPROTEGERIN; ACIDIFICATION; ACTIVATION;
D O I
10.1007/s00223-013-9741-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the bone remodeling process that takes place throughout the skeleton at bone multicellular units, intercellular communication processes are crucial. The osteoblast lineage has long been known to program osteoclast formation and hence resorption, but the preservation of bone mass and integrity requires tight control of remodeling. This needs local controls that ensure availability of mesenchymal precursors and the provision of local signals that promote differentiation through the osteoblast lineage. Some signals can come from growth factors released from resorbed bone matrix, and there is increasing evidence that the osteoclast lineage itself produces factors that can either enhance or inhibit osteoblast differentiation and hence bone formation. A number of such factors have been identified from predominantly in vitro experiments. The coupling of bone formation to resorption is increasingly recognized as a complex, dynamic process that results from the input of many local factors of cell and matrix origin that can either promote or inhibit bone formation.
引用
收藏
页码:88 / 97
页数:10
相关论文
共 87 条
[1]   Osteoclast-derived serum tartrate-resistant acid phosphatase 5b in Albers-Schonberg disease (Type II autosomal dominant osteopetrosis) [J].
Alatalo, SL ;
Ivaska, KK ;
Waguespack, SG ;
Econs, MJ ;
Väänänen, HK ;
Halleen, JM .
CLINICAL CHEMISTRY, 2004, 50 (05) :883-890
[2]  
Allan EH, 2008, J BONE MINER RES, V23, P1170, DOI [10.1359/jbmr.080324, 10.1359/JBMR.080324]
[3]   A Physical Mechanism for Coupling Bone Resorption and Formation in Adult Human Bone [J].
Andersen, Thomas Levin ;
Sondergaard, Teis Esben ;
Skorzynska, Katarzyna Ewa ;
Dagnaes-Hansen, Frederik ;
Plesner, Trine Lindhardt ;
Hauge, Ellen Margrethe ;
Plesner, Torben ;
Delaisse, Jean-Marie .
AMERICAN JOURNAL OF PATHOLOGY, 2009, 174 (01) :239-247
[4]   A TNF receptor loop peptide mimic blocks RANK ligand-induced signaling, bone resorption, and bone loss [J].
Aoki, Kazuhiro ;
Saito, Hiroaki ;
Itzstein, Cecile ;
Ishiguro, Masaji ;
Shibata, Tatsuya ;
Blanque, Roland ;
Mian, Anower Hussain ;
Takahashi, Mariko ;
Suzuki, Yoshifumi ;
Yoshimatsu, Masako ;
Yamaguchi, Akira ;
Deprez, Pierre ;
Mollat, Patrick ;
Murali, Ramachandran ;
Ohya, Keiichi ;
Horne, William C. ;
Baron, Roland .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (06) :1525-1534
[5]   Advances in the osteoblast lineage [J].
Aubin, JE .
BIOCHEMISTRY AND CELL BIOLOGY, 1998, 76 (06) :899-910
[6]   CELL-MEDIATED EXTRACELLULAR ACIDIFICATION AND BONE-RESORPTION - EVIDENCE FOR A LOW PH IN RESORBING LACUNAE AND LOCALIZATION OF A 100-KD LYSOSOMAL MEMBRANE-PROTEIN AT THE OSTEOCLAST RUFFLED BORDER [J].
BARON, R ;
NEFF, L ;
LOUVARD, D ;
COURTOY, PJ .
JOURNAL OF CELL BIOLOGY, 1985, 101 (06) :2210-2222
[7]   Minireview:: Targeting the Wnt/β-catenin pathway to regulate bone formation in the adult skeleton [J].
Baron, Roland ;
Rawadi, Georges .
ENDOCRINOLOGY, 2007, 148 (06) :2635-2643
[8]   ULTRASTRUCTURAL INVESTIGATIONS OF BONE RESORPTIVE CELLS IN 2 TYPES OF AUTOSOMAL-DOMINANT OSTEOPETROSIS [J].
BOLLERSLEV, J ;
MARKS, SC ;
POCKWINSE, S ;
KASSEM, M ;
BRIXEN, K ;
STEINICHE, T ;
MOSEKILDE, L .
BONE, 1993, 14 (06) :865-869
[9]  
Boyce BF, 2013, GENETICS BONE BIOL
[10]   Osteoclast differentiation and activation [J].
Boyle, WJ ;
Simonet, WS ;
Lacey, DL .
NATURE, 2003, 423 (6937) :337-342