Department of Biochemistry, University of Missouri, Columbia, MO 65211, USA.
Department of Child Health, University of Missouri, Columbia, MO 65212, USA.
Int J Mol Sci. 2021 May 7;22(9):4963. doi: 10.3390/ijms22094963.
Bone and muscle are highly synergistic tissues that communicate extensively via mechanotransduction and biochemical signaling. Osteogenesis imperfecta (OI) is a heritable connective tissue disorder of severe bone fragility and recently recognized skeletal muscle weakness. The presence of impaired bone and muscle in OI leads to a continuous cycle of altered muscle-bone crosstalk with weak muscles further compromising bone and vice versa. Currently, there is no cure for OI and understanding the pathogenesis of the skeletal muscle weakness in relation to the bone pathogenesis of OI in light of the critical role of muscle-bone crosstalk is essential to developing and identifying novel therapeutic targets and strategies for OI. This review will highlight how impaired skeletal muscle function contributes to the pathophysiology of OI and how this phenomenon further perpetuates bone fragility.
骨骼和肌肉是高度协同的组织,通过机械转导和生化信号广泛交流。成骨不全症(OI)是一种遗传性结缔组织疾病,表现为严重的骨骼脆弱,最近还被认为与骨骼肌肉无力有关。OI 中存在的骨骼和肌肉受损导致肌肉-骨骼相互作用发生改变,形成恶性循环,使肌肉进一步受损,骨骼也同样受到影响。目前,OI 尚无治愈方法,了解骨骼肌肉无力与 OI 的骨骼发病机制之间的关系,以及肌肉-骨骼相互作用的关键作用,对于开发和确定 OI 的新治疗靶点和策略至关重要。本文将重点介绍骨骼肌肉功能受损如何导致 OI 的病理生理学,并探讨这一现象如何进一步导致骨骼脆弱。