Center for Cellular and Molecular Engineering, Department of Orthopaedic Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Institute for Tissue Engineering and Regenerative Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.
J Cell Mol Med. 2020 Oct;24(19):11046-11055. doi: 10.1111/jcmm.15735. Epub 2020 Aug 27.
Heterotopic ossification (HO) is a pathological condition of abnormal bone formation in soft tissue. Three factors have been proposed as required to induce HO: (a) osteogenic precursor cells, (b) osteoinductive agents and (c) an osteoconductive environment. Since Urist's landmark discovery of bone induction in skeletal muscle tissue by demineralized bone matrix, it is generally believed that skeletal muscle itself is a conductive environment for osteogenesis and that resident progenitor cells in skeletal muscle are capable of differentiating into osteoblast to form bone. However, little is known about the naturally occurring osteoinductive agents that triggered this osteogenic response in the first place. This article provides a review of the emerging findings regarding distinct types of HO to summarize the current understanding of HO mechanisms, with special attention to the osteogenic factors that are induced following injury. Specifically, we hypothesize that muscle injury-induced up-regulation of local bone morphogenetic protein-7 (BMP-7) level, combined with glucocorticoid excess-induced down-regulation of circulating transforming growth factor-β1 (TGF-β1) level, could be an important causative mechanism of traumatic HO formation.
异位骨化(HO)是一种软组织中异常骨形成的病理状况。有三个因素被认为是诱导 HO 所必需的:(a)成骨前体细胞,(b)成骨诱导剂和(c)成骨诱导环境。自从 Urist 发现脱矿骨基质在骨骼肌组织中诱导骨形成以来,人们普遍认为骨骼肌本身就是成骨的传导环境,并且骨骼肌中的固有祖细胞能够分化为成骨细胞形成骨。然而,对于最初触发这种成骨反应的天然存在的成骨诱导剂知之甚少。本文综述了异位骨化的最新研究结果,总结了目前对 HO 机制的认识,特别关注损伤后诱导的成骨因子。具体而言,我们假设肌肉损伤诱导的局部骨形态发生蛋白 7(BMP-7)水平上调,加上糖皮质激素过量诱导的循环转化生长因子-β1(TGF-β1)水平下调,可能是创伤性 HO 形成的重要致病机制。