Wood Charles L, Pajevic Paola Divieti, Gooi Jonathan H
Department of Medicine, St. Vincent's Hospital Melbourne, The University of Melbourne, Melbourne, VIC 3065, Australia.
Molecular and Cell Biology, Goldman School of Dental Medicine, Boston University, Boston, MA, United States.
Bone Rep. 2017 Mar 2;6:74-80. doi: 10.1016/j.bonr.2017.02.007. eCollection 2017 Jun.
It is generally accepted that bone and muscle possess the capacity to act in an autocrine, paracrine, or endocrine manner, with a growing body of evidence that suggests muscle can secrete muscle specific cytokines or "myokines", which influence bone metabolism. However, there has been little investigation into the identity of bone specific cytokines that modulate skeletal muscle differentiation and function. This study aimed to elucidate the influence of osteocytes on muscle progenitor cells in vitro and to identify potential bone specific cytokines or "osteokines". We treated C2C12 myoblasts with media collected from differentiated osteocytes (Ocy454 cells) grown in 3D, either under static or fluid flow culture conditions (2 dynes/cm). C2C12 differentiation was significantly inhibited with a 75% reduction in the number of myofibers formed. mRNA analysis revealed a significant reduction in the expression of myogenic regulatory genes. Cytokine array analysis on the conditioned media demonstrated that osteocytes produce a significant number of cytokines "osteokines" capable of inhibiting myogenesis. Furthermore, we demonstrated that when osteocytes are mechanically activated they induce a greater inhibitory effect on myogenesis compared to a static state. Lastly, we identified the downregulation of numerous cytokines, including , , , , and , involved in myogenesis, which may lead to future investigation of the role "osteokines" play in musculoskeletal health and pathology.
人们普遍认为,骨骼和肌肉具有以自分泌、旁分泌或内分泌方式发挥作用的能力,越来越多的证据表明,肌肉可以分泌影响骨代谢的肌肉特异性细胞因子或“肌动蛋白”。然而,对于调节骨骼肌分化和功能的骨特异性细胞因子的身份,研究甚少。本研究旨在阐明骨细胞在体外对肌肉祖细胞的影响,并确定潜在的骨特异性细胞因子或“骨动蛋白”。我们用在3D条件下生长的分化骨细胞(Ocy454细胞)收集的培养基处理C2C12成肌细胞,培养条件为静态或流体流动培养条件(2达因/平方厘米)。C2C12分化受到显著抑制,形成的肌纤维数量减少了75%。mRNA分析显示,生肌调节基因的表达显著降低。对条件培养基进行细胞因子阵列分析表明,骨细胞产生大量能够抑制肌生成的细胞因子“骨动蛋白”。此外,我们证明,与静态状态相比,当骨细胞被机械激活时,它们对肌生成的抑制作用更大。最后,我们确定了多种参与肌生成的细胞因子的下调,包括 、 、 、 和 ,这可能会导致未来对“骨动蛋白”在肌肉骨骼健康和病理学中所起作用的研究。