Cell-to-cell communication in guided bone regeneration: molecular and cellular mechanisms

被引:34
|
作者
Gruber, Reinhard [1 ,2 ]
Stadlinger, Bernd [3 ]
Terheyden, Hendrik [4 ]
机构
[1] Med Univ Vienna, Dept Oral Biol, Sensengasse 2a, A-1090 Vienna, Austria
[2] Univ Bern, Sch Dent Med, Dept Prevent Restorat & Pediat Dent, Freiburgstr 7, CH-3010 Bern, Switzerland
[3] Univ Zurich, Clin Craniomaxillofacial & Oral Surg, Zurich, Switzerland
[4] Red Cross Hosp, Dept Oral & Maxillofacial Surg, Kassel, Germany
关键词
bone regeneration; guided tissue regeneration; structural biology; tissue physiology; wound healing; FRACTURE REPAIR; TNF-ALPHA; OSTEOBLAST FUNCTION; SKELETAL; AUGMENTATION; MACROPHAGES; ANGIOGENESIS; RESORPTION; DIFFERENTIATION; HOMEOSTASIS;
D O I
10.1111/clr.12929
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
This overview provides insights into the molecular and cellular mechanisms involved in guided bone regeneration, in particular focusing on aspects presented in the 3D movie, Cell-To-Cell Communication in Guided Bone Regeneration. The information presented here is based almost exclusively on genetic mouse models in which single genes can be deleted or overexpressed, even in a specific cell type. This information needs to be extrapolated to humans and related to aspects relevant to graft consolidation under the clinical parameters of guided bone regeneration. The overview follows the ground tenor of the Cell-To-Cell Communication series and focuses on aspects of cell-to-cell communication in bone regeneration and guided bone regeneration. Here, we discuss (1) the role of inflammation during bone regeneration, including (2) the importance of the fibrin matrix, and (3) the pleiotropic functions of macrophages. We highlight (4) the origin of bone-forming osteoblasts and bone-resorbing osteoclasts as well as (5) what causes a progenitor cell to mature into an effector cell. (6) We touch on the complex bone adaptation and maintenance after graft consolidation and (7) how osteocytes control this process. Finally, we speculate on (8) how barrier membranes and the augmentation material can modulate graft consolidation.
引用
收藏
页码:1139 / 1146
页数:8
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