Mechanisms of bone repair and regeneration

被引:356
作者
Deschaseaux, Frederic [1 ,2 ]
Sensebe, Luc [1 ,2 ]
Heymann, Dominique [3 ]
机构
[1] Etab Francais Sang Ctr Atlantique, Grp Rech Cellules Souches Mesenchymateuses GECSoM, Tours, France
[2] Univ Tours, Fac Med, EA3855, Tours, France
[3] Nantes Atlantique Univ, Univ Nantes, Lab Physiopathol Resorpt Osseuse & Therapie Tumeu, INSERM,U957,EA3822, Nantes, France
关键词
MESENCHYMAL STEM-CELLS; OSTEOBLAST DIFFERENTIATION; OSTEOGENIC DIFFERENTIATION; MORPHOGENETIC PROTEIN-2; TRANSCRIPTION FACTOR; GROWTH-PLATE; CHONDROCYTE PROLIFERATION; P38; MAPK; TGF-BETA; KAPPA-B;
D O I
10.1016/j.molmed.2009.07.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Bone problems can have a highly deleterious impact on life and society, therefore understanding the mechanisms of bone repair is important. In vivo studies show that bone repair processes in adults resemble normal development of the skeleton during embryogenesis, which can thus be used as a model. In addition, recent studies of skeletal stem cell biology have underlined several crucial molecular and cellular processes in bone formation. Hedgehog, parathyroid hormone-related protein, Writ, bone morphogenetic proteins and mitogen-activated protein kinases are the main molecular players, and osteoclasts and mesenchymal stem cells are the main cells involved in these processes. However, questions remain regarding the precise mechanisms of bone formation, how the different molecular processes interact, and the real identity of regenerative cells. Here, we review recent studies of bone regeneration and repair. A better understanding of the underlying mechanisms is expected to facilitate the development of new strategies for improving bone repair.
引用
收藏
页码:417 / 429
页数:13
相关论文
共 100 条
[1]
The transcrintion factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6 [J].
Akiyama, H ;
Chaboissier, MC ;
Martin, JF ;
Schedl, A ;
de Crombrugghe, B .
GENES & DEVELOPMENT, 2002, 16 (21) :2813-2828
[2]
Immune interactions with CD4+ T cells promote the development of functional osteoclasts from murine CD11c+ dendritic cells [J].
Alnaeeli, Mawadda ;
Penninger, Josef M. ;
Teng, Yen-Tung Andy .
JOURNAL OF IMMUNOLOGY, 2006, 177 (05) :3314-3326
[3]
Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis, and articular cartilage [J].
Anderson, HC ;
Hodges, PT ;
Aguilera, XM ;
Missana, L ;
Moylan, PE .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2000, 48 (11) :1493-1502
[4]
Baek WY, 2009, J BONE MINER RES, V24, P1055, DOI [10.1359/JBMR.081248, 10.1359/jbmr.081248]
[5]
Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb patterning and skeletogenesis [J].
Bandyopadhyay, Amitabha ;
Tsuji, Kunikazu ;
Cox, Karen ;
Harfe, Brian D. ;
Rosen, Vicki ;
Tabin, Clifford J. .
PLOS GENETICS, 2006, 2 (12) :2116-2130
[6]
RANKL, RANK, osteoprotegerin:: key partners of osteoimmunology and vascular diseases [J].
Baud'huin, M. ;
Lamoureuxa, F. ;
Duplomba, L. ;
Redini, F. ;
Heymann, D. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2007, 64 (18) :2334-2350
[7]
Regulation of osteoblastogenesis and bone mass by Wnt10b [J].
Bennett, CN ;
Longo, KA ;
Wright, WS ;
Suva, LJ ;
Lane, TF ;
Hankenson, KD ;
MacDougald, OA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (09) :3324-3329
[8]
p38 mitogen-activated protein kinase regulates canonical Wnt-β-catenin signaling by inactivation of GSK3β [J].
Bikkavilli, Rama Kamesh ;
Feigin, Michael E. ;
Malbon, Craig C. .
JOURNAL OF CELL SCIENCE, 2008, 121 (21) :3598-3607
[9]
The Wnt antagonist secreted frizzled-related protein-1 controls osteoblast and osteocyte apoptosis [J].
Bodine, PVN ;
Billiard, J ;
Moran, RA ;
Ponce-de-Leon, H ;
McLarney, S ;
Mangine, A ;
Scrimo, MJ ;
Bhat, RA ;
Stauffer, B ;
Green, J ;
Stein, GS ;
Lian, JB ;
Komm, BS .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2005, 96 (06) :1212-1230
[10]
BMP-2 and insulin-like growth factor-I mediate osterix (Osx) expression in human mesenchymal stem cells via the MAPK and protein kinase D signaling pathways [J].
Celil, AB ;
Campbell, PG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (36) :31353-31359