The role of endothelial-mesenchymal transition in heterotopic ossification

被引:112
|
作者
Medici, Damian [1 ,2 ]
Olsen, Bjorn R. [2 ,3 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Div Matrix Biol,Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Sch Dent Med, Dept Dev Biol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
关键词
ENDOTHELIAL-MESENCHYMAL TRANSITION; ENDMT; EMT; HETEROTOPIC OSSIFICATION; FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP; BMP; TGF-BETA; STEM CELLS; PROGENITOR CELLS; BONE-FORMATION; I RECEPTOR; SIGNAL-TRANSDUCTION; PROGRESSIVA FOP; FIBROSIS; SKELETOGENESIS; TRANSFORMATION; FIBROBLASTS; CONTRIBUTES;
D O I
10.1002/jbmr.1691
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Heterotopic ossification (HO) is a process by which bone forms in soft tissues, in response to injury, inflammation, or genetic disease. This usually occurs by initial cartilage formation, followed by endochondral ossification. A rare disease called fibrodysplasia ossificans progressiva (FOP) allows this mechanism to be induced by a combination of genetic mutation and acute inflammatory responses. FOP patients experience progressive HO throughout their lifetime and form an ectopic skeleton. Recent studies on FOP have suggested that heterotopic cartilage and bone is of endothelial origin. Vascular endothelial cells differentiate into skeletal cells through a mesenchymal stem cell intermediate that is generated by endothelial-mesenchymal transition (EndMT). Local inflammatory signals and/or other changes in the tissue microenvironment mediate the differentiation of endothelial-derived mesenchymal stem cells into chondrocytes and osteoblasts to induce HO. We discuss the current evidence for the endothelial contribution to heterotopic bone formation. (C) 2012 American Society for Bone and Mineral Research.
引用
收藏
页码:1619 / 1622
页数:4
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