A Physical Mechanism for Coupling Bone Resorption and Formation in Adult Human Bone

被引:239
作者
Andersen, Thomas Levin [1 ]
Sondergaard, Teis Esben [1 ]
Skorzynska, Katarzyna Ewa [1 ]
Dagnaes-Hansen, Frederik [3 ]
Plesner, Trine Lindhardt [4 ]
Hauge, Ellen Margrethe [5 ]
Plesner, Torben [2 ]
Delaisse, Jean-Marie [1 ]
机构
[1] Univ So Denmark, IRS CSFU, Vejle Hosp, Dept Clin Cell Biol, DK-7100 Vejle, Denmark
[2] Univ So Denmark, IRS CSFU, Vejle Hosp, Dept Hematol, DK-7100 Vejle, Denmark
[3] Univ Aarhus, Dept Microbiol, Aarhus, Denmark
[4] Aarhus Univ Hosp, Inst Pathol, DK-8000 Aarhus, Denmark
[5] Aarhus Univ Hosp, Dept Rheumatol, DK-8000 Aarhus, Denmark
关键词
ENDOTHELIAL GROWTH-FACTOR; OSTEOBLAST-LINEAGE CELLS; REMODELING COMPARTMENT; SKELETAL DEVELOPMENT; OSTEOCLAST FORMATION; FACTOR VEGF; EXPRESSION; HYPOXIA; MARROW; DIFFERENTIATION;
D O I
10.2353/ajpath.2009.080627
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
During skeletal remodeling, pre-osteoclasts and pre-ostcoblasts are targeted to critical sites of the bone to resorb and reconstruct bone matrix, respectively. Coordination of site-specific recruitment of these two cell types is a prerequisite to maintain the specific architecture of each bone within strict limits throughout adult fife. Here, we determined that the bone marrow microanatomy adjacent to remodeling areas is a central player in this process. By using histomorphometry and multiple immunostainings, we demonstrated in biopsies exhibiting coupled bone resorption and formation that osteoclasts and osteoblasts on the bone surface were always covered by a canopy of flat cells expressing osteoblast markers. In contrast, in biopsies in which this canopy was disrupted, bone formation was deficient. Three-dimensional visualizations revealed that this canopy covered the entire remodeling site and was associated with capillaries, thereby forming a previously unrecognized microanatomical entity. Furthermore, pre-osteoclasts were positioned along these capillaries. These findings led to a model that implicates vasculature in the site-specific recruitment of osteoclasts and osteoblasts and embraces the current knowledge on the molecular mechanism of bone remodeling. (Am J Pathol 2009, 174:239-247; DOI. 10.2353/ajpath.2009.080627)
引用
收藏
页码:239 / 247
页数:9
相关论文
共 51 条
[31]  
Kindle L, 2006, J BONE MINER RES, V21, P193, DOI 10.1359/JBMR.051027
[32]   Activation of the transcription factor HIF-1 and its target genes, VEGF, HO-1, iNOS, during fracture repair [J].
Komatsu, DE ;
Hadjiargyrou, M .
BONE, 2004, 34 (04) :680-688
[33]   Effect of ovariectomy on intraosseous vascularization and bone remodelling in rats: Action of tiludronate [J].
Laroche, M ;
Barbier, A ;
Ludot, I ;
Vernhet, C ;
Thiechart, M ;
Viguier, G ;
Mazieres, B .
OSTEOPOROSIS INTERNATIONAL, 1996, 6 (02) :127-129
[34]   Osteoclast-derived activity in the coupling of bone formation to resorption [J].
Martin, TJ ;
Sims, NA .
TRENDS IN MOLECULAR MEDICINE, 2005, 11 (02) :76-81
[35]   Osteoclast-osteoblast communication [J].
Matsuo, Koichi ;
Irie, Naoko .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2008, 473 (02) :201-209
[36]   THE MICRO-VASCULAR BED OF FATTY BONE-MARROW IN THE ADULT BEAGLE [J].
MILLER, SC ;
JEE, WSS .
METABOLIC BONE DISEASE & RELATED RESEARCH, 1980, 2 (04) :239-246
[37]   Skeletal stem/osteoprogenitor cells:: Current concepts, alternate hypotheses, and relationship to the bone remodeling compartment [J].
Modder, Ulrike I. ;
Khosla, Sundeep .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2008, 103 (02) :393-400
[38]   Expression of angiogenic factors during distraction osteogenesis [J].
Pacicca, DM ;
Patel, N ;
Lee, C ;
Salisbury, K ;
Lehmann, W ;
Carvalho, R ;
Gerstenfeld, LC ;
Einhorn, TA .
BONE, 2003, 33 (06) :889-898
[39]   The mechanism of coupling: A role for the vasculature [J].
Parfitt, AM .
BONE, 2000, 26 (04) :319-323
[40]   The bone remodeling compartment: A circulatory function for bone lining cells [J].
Parfitt, AM .
JOURNAL OF BONE AND MINERAL RESEARCH, 2001, 16 (09) :1583-1585