Literature DB >> 18692584

Bone remodeling during fracture repair: The cellular picture.

Aaron Schindeler1, Michelle M McDonald, Paul Bokko, David G Little.   

Abstract

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.

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Year:  2008        PMID: 18692584     DOI: 10.1016/j.semcdb.2008.07.004

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  223 in total

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Review 4.  Overview of biological mechanisms and applications of three murine models of bone repair: closed fracture with intramedullary fixation, distraction osteogenesis, and marrow ablation by reaming.

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7.  Inhibition of β-catenin signaling in chondrocytes induces delayed fracture healing in mice.

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8.  Bone healing in an aged murine fracture model is characterized by sustained callus inflammation and decreased cell proliferation.

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Journal:  J Orthop Res       Date:  2017-10-09       Impact factor: 3.494

Review 9.  Biomimetic Approaches for Bone Tissue Engineering.

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Journal:  Tissue Eng Part B Rev       Date:  2017-01-18       Impact factor: 6.389

10.  Hyperlipidemia compromises homing efficiency of systemically transplanted BMSCs and inhibits bone regeneration.

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Journal:  Int J Clin Exp Pathol       Date:  2014-03-15
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