Nelson Emily R, Wong Victor W, Krebsbach Paul H, Wang Stewart C, Levi Benjamin
Department of Surgery, Plastic and Reconstructive Surgery Division, Hagey Laboratory for Pediatric Regenerative Medicine, Stanford University School of Medicine, Stanford, California, USA.
J Burn Care Res. 2012 Jul-Aug;33(4):463-70. doi: 10.1097/BCR.0b013e31825af547.
Heterotopic ossification (HO), or the abnormal development of bone tissue in soft-tissue locations, can be physically debilitating and clinically devastating. For unclear reasons, HO is highly associated with burn injury. The objective of this review is to summarize 1) cells that are responsible for HO, 2) in vitro and in vivo models of HO and how they have contributed to our current knowledge of the disease process, 3) the effects of the adipose compartment on HO, 4) the effects of inflammation on HO, and 5) the effects of mesenchymal stem cells (MSCs) on HO. Preclinical models of HO suggest several possible mechanisms for the development of this pathologic process, including progenitor cell differentiation and paracrine modulation of local inflammatory responses. Further studies are needed to elucidate the molecular mechanisms driving HO so that targeted therapies can be developed. Current literature supports a role for MSCs in modulating heterotopic bone formation, and direct manipulation of MSCs might one day be used to prevent and treat HO.
异位骨化(HO),即骨组织在软组织部位异常发育,会导致身体功能衰弱并造成临床损害。原因不明的是,HO与烧伤密切相关。本综述的目的是总结:1)导致HO的细胞;2)HO的体外和体内模型以及它们如何增进了我们对疾病过程的当前认识;3)脂肪组织对HO的影响;4)炎症对HO的影响;5)间充质干细胞(MSC)对HO的影响。HO的临床前模型提示了这一病理过程发展的几种可能机制,包括祖细胞分化和局部炎症反应的旁分泌调节。需要进一步研究以阐明驱动HO的分子机制,从而开发出靶向治疗方法。当前文献支持MSC在调节异位骨形成中的作用,对MSC的直接操控或许有朝一日可用于预防和治疗HO。