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内皮-间充质转化在异位骨化中的作用。

The role of endothelial-mesenchymal transition in heterotopic ossification.

机构信息

Division of Matrix Biology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115, USA.

出版信息

J Bone Miner Res. 2012 Aug;27(8):1619-22. doi: 10.1002/jbmr.1691. Epub 2012 Jul 2.

Abstract

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.

摘要

异位骨化(HO)是一种在骨骼形成的过程中,在软组织结构中,通过受伤、炎症或遗传疾病来响应。这通常通过初始软骨形成,然后通过软骨内骨化来发生。一种罕见的疾病叫做纤维发育不良性骨化性进展(FOP),允许这种机制通过遗传突变和急性炎症反应的组合来诱导。FOP 患者在他们的一生中经历进行性的 HO,并形成异位骨骼。最近对 FOP 的研究表明,异位软骨和骨来源于内皮细胞。血管内皮细胞通过内皮-间充质转化(EndMT)产生的间充质干细胞中间体分化为成骨细胞。局部炎症信号和/或组织微环境的其他变化调节内皮衍生的间充质干细胞向软骨细胞和成骨细胞的分化,从而诱导 HO。我们讨论了目前关于内皮细胞对异位骨形成的贡献的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aba9/3432417/1b4bee05a98d/nihms397201f1.jpg

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