Division of Orthopaedic Surgery, Department of Surgery, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Centre for Orthopaedic Translational Research, School of Biomedical Sciences, University of Western Australia, Nedlands, Western Australia, Australia.
FASEB J. 2018 Sep;32(9):4804-4814. doi: 10.1096/fj.201701384R. Epub 2018 Mar 29.
The tendon is a mechanosensitive tissue, but little is known about how mechanical stimulation selectively signals tenogenic differentiation and neo-tendon formation. In this study, we compared the impact of uniaxial and biaxial mechanical loading on tendon-derived stem cells (TDSCs). Our data show that there are variations in cell signaling and cell differentiation of mouse TDSCs in response to uniaxial and biaxial loading in monolayer culture. Whereas uniaxial loading induced TDSCs toward tenogenic and osteogenic differentiation, biaxial loading induced osteogenic, adipogenic, and chondrogenic differentiation of TDSCs. Furthermore, by applying uniaxial loading on 3-dimensional (3D) TDSC constructs, tenogenic-specific differentiation and neo-tendon formation were observed, results that were replicated in human TDSCs. We also showed that uniaxial loading induced PKB (AKT) phosphorylation (pAKT), whereas biaxial loading induced pERK. Most importantly, we found that inhibition of the PI3K/AKT signaling pathway could attenuate tenogenic differentiation and tendon formation in 3D TDSC constructs subjected to uniaxial loading. Taken together, our study highlights the importance of appropriate mechanobiological stimulation in 3D cell niches on tendon-like tissue formation and demonstrates that uniaxial mechanical loading plays an essential role in tenogenic differentiation and tendon formation by activating the PI3K/AKT signaling pathway.-Wang, T., Thien, C., Wang, C., Ni, M., Gao, J., Wang, A., Jiang, Q., Tuan, R. S., Zheng, Q., Zheng, M. H. 3D uniaxial mechanical stimulation induces tenogenic differentiation of tendon-derived stem cells through a PI3K/AKT signaling pathway.
肌腱是一种力敏组织,但对于机械刺激如何选择性地发出信号以促进肌腱细胞分化和形成新的肌腱知之甚少。在这项研究中,我们比较了单轴和双轴机械加载对肌腱衍生干细胞(TDSCs)的影响。我们的数据表明,在单层培养中,对单轴和双轴加载的反应中,鼠 TDSCs 的细胞信号和细胞分化存在差异。单轴加载诱导 TDSCs 向肌腱和成骨分化,而双轴加载诱导 TDSCs 向成骨、脂肪和成软骨分化。此外,通过对 3D TDSC 构建体施加单轴加载,观察到了肌腱特异性分化和新的肌腱形成,这些结果在人 TDSCs 中得到了复制。我们还表明,单轴加载诱导 PKB(AKT)磷酸化(pAKT),而双轴加载诱导 pERK。最重要的是,我们发现抑制 PI3K/AKT 信号通路可以减弱在单轴加载的 3D TDSC 构建体中肌腱样组织形成的肌腱细胞分化和肌腱形成。综上所述,我们的研究强调了在 3D 细胞微环境中适当的机械生物学刺激对肌腱样组织形成的重要性,并表明单轴机械加载通过激活 PI3K/AKT 信号通路在肌腱细胞分化和肌腱形成中起着至关重要的作用。