Bone remodeling during fracture repair: The cellular picture

被引:644
作者
Schindeler, Aaron [1 ,2 ]
McDonald, Michelle M. [1 ]
Bokko, Paul [1 ]
Little, David G. [1 ,2 ]
机构
[1] Childrens Hosp, Dept Orthopaed Res & Biotechnol, Westmead, NSW 2145, Australia
[2] Univ Sydney, Fac Med, Discipline Paediat & Child Hlth, Sydney, NSW 2006, Australia
基金
英国医学研究理事会;
关键词
Bone remodeling; Fracture; Fracture healing; Bone repair; Bisphosphonates;
D O I
10.1016/j.semcdb.2008.07.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fracture healing is a complex event that involves the coordination of a variety of different processes. Repair is typically characterized by four overlapping stages: the initial inflammatory response, soft callus formation, hard callus formation, initial bony union and bone remodeling. However, repair can also be seen to represent a juxtaposition of two distinct forces: anabolism or tissue formation, and catabolism or remodeling. These anabolic/catabolic concepts are useful for understanding bone repair without giving the false impression of temporally distinct stages that operate independently. They are also relevant when considering intervention. In normal bone development, bone remodeling conventionally refers to the removal of calcified bone tissue by osteoclasts. However, in the context of bone repair there are two phases of tissue catabolism: the removal of the initial cartilaginous soft callus, followed by the eventual remodeling of the bony hard callus. In this review, we have attempted to examine catabolism/remodeling in fractures in a systematic fashion. The first section briefly summarizes the traditional four-stage view of fracture repair in a physiological manner. The second section highlights some of the limitations of using a temporal rather than process-driven model and summarizes the anabolic/catabolic paradigm of fracture repair. The third section examines the cellular participants in soft callus remodeling and in particular the role of the osteoclast in endochondral ossification. Finally, the fourth section examines the effects of delaying osteoclast-dependent hard callus remodeling and also poses questions regarding the crosstalk between anabolism and catabolism in the latter stages of fracture repair. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:459 / 466
页数:8
相关论文
共 84 条
  • [1] Molecular mechanisms controlling bone formation during fracture healing and distraction osteogenesis
    Ai-Aql, Z. S.
    Alagl, A. S.
    Graves, D. T.
    Gerstenfeld, L. C.
    Einhorn, T. A.
    [J]. JOURNAL OF DENTAL RESEARCH, 2008, 87 (02) : 107 - 118
  • [2] A single systemic dose of pamidronate improves bone mineral content and accelerates restoration of strength in a rat model of fracture repair
    Amanat, N
    Brown, R
    Bilston, LE
    Little, DG
    [J]. JOURNAL OF ORTHOPAEDIC RESEARCH, 2005, 23 (05) : 1029 - 1034
  • [3] Optimal timing of a single dose of zoledronic acid to increase strength in rat fracture repair
    Amanat, Negin
    McDonald, Michelle
    Godfrey, Craig
    Bilston, Lynne
    Little, David
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 2007, 22 (06) : 867 - 876
  • [4] Adult mesenchymal stem cells: characterization, differentiation, and application in cell and gene therapy
    Baksh, D
    Song, L
    Tuan, RS
    [J]. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2004, 8 (03) : 301 - 316
  • [5] Growth factor regulation of fracture repair
    Barnes, GL
    Kostenuik, PJ
    Gerstenfeld, LC
    Einhorn, TA
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 1999, 14 (11) : 1805 - 1815
  • [6] Role of Matrix Metalloproteinase 13 in Both Endochondral and Intramembranous Ossification during Skeletal Regeneration
    Behonick, Danielle J.
    Xing, Zhiqing
    Lieu, Shirley
    Buckley, Jenni M.
    Lotz, Jeffrey C.
    Marcucio, Ralph S.
    Werb, Zena
    Miclau, Theodore
    Colnot, Celine
    [J]. PLOS ONE, 2007, 2 (11):
  • [7] SOST/sclerostin, an osteocyte-derived negative regulator of bone formation
    Bezooijen, RL
    ten Dijke, P
    Papapoulos, SE
    Löwik, CWGM
    [J]. CYTOKINE & GROWTH FACTOR REVIEWS, 2005, 16 (03) : 319 - 327
  • [8] Mechanisms of disease: roles of OPG, RANKL and RANK in the pathophysiology of skeletal metastasis
    Blair, JM
    Zhou, H
    Seibel, MJ
    Dunstan, CR
    [J]. NATURE CLINICAL PRACTICE ONCOLOGY, 2006, 3 (01): : 41 - 49
  • [9] BOLANDER ME, 1992, P SOC EXP BIOL MED, V200, P165
  • [10] The vascularity of atrophic non-unions
    Brownlow, HC
    Reed, A
    Simpson, AHRW
    [J]. INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED, 2002, 33 (02): : 145 - 150