College of Engineering, University of Missouri, Columbia, Missouri, United States of America.
Spanish National Cancer Research Centre, Madrid, Spain.
PLoS One. 2019 Oct 4;14(10):e0223245. doi: 10.1371/journal.pone.0223245. eCollection 2019.
Mechanical loading is essential for the maintenance of musculoskeletal homeostasis. Cartilage has been demonstrated to be highly mechanoresponsive, but the mechanisms by which chondrocytes respond to mechanical stimuli are not clearly understood. The goal of the study was to determine how LRP4, LRP5, and LRP6 within canonical Wnt-signaling are regulated in simulated microgravity and cyclic hydrostatic pressure, and to investigate the potential role of LRP 4/5/6 in cartilage degeneration. Rat chondrosacroma cell (RCS) pellets were stimulated using either cyclic hydrostatic pressure (1Hz, 7.5 MPa, 4hr/day) or simulated microgravity in a rotating wall vessel (RWV) bioreactor (11RPM, 24hr/day). LRP4/5/6 mRNA expression was assessed by RT-qPCR and LRP5 protein expression was determined by fluorescent immunostaining. To further evaluate our in vitro findings in vivo, mice were subjected to hindlimb suspension for 14 days and the femoral heads stained for LRP5 expression. We found that, in vitro, LRP4/5/6 mRNA expression is modulated in a time-dependent manner by mechanical stimulation. Additionally, LRP5 protein expression is upregulated in response to both simulated microgravity and cyclic hydrostatic pressure. LRP5 is also upregulated in vivo in the articular cartilage of hindlimb suspended mice. This is the first study to examine how LRP4/5/6, critical receptors within musculoskeletal biology, respond to mechanical stimulation. Further elucidation of this mechanism could provide significant clinical benefit for the identification of pharmaceutical targets for the maintenance of cartilage health.
力学加载对于维持肌肉骨骼系统的内稳态至关重要。软骨具有高度的力学响应性,但软骨细胞对力学刺激的反应机制尚不清楚。本研究旨在确定经典 Wnt 信号通路中的 LRP4、LRP5 和 LRP6 如何在模拟微重力和循环流体静压下被调节,并探讨 LRP4/5/6 在软骨退变中的潜在作用。通过使用循环流体静压(1Hz,7.5MPa,每天 4 小时)或旋转壁式生物反应器(RWV)中的模拟微重力(11RPM,每天 24 小时)刺激大鼠软骨肉瘤细胞(RCS)球。通过 RT-qPCR 评估 LRP4/5/6mRNA 表达,通过荧光免疫染色测定 LRP5 蛋白表达。为了进一步评估我们在体内的体外发现,将小鼠的后肢悬吊 14 天,并对 LRP5 表达进行股骨头部染色。我们发现,在体外,LRP4/5/6mRNA 表达随时间推移受力学刺激的调节。此外,LRP5 蛋白表达对模拟微重力和循环流体静压均有上调。LRP5 在悬吊后肢小鼠的关节软骨中也在体内上调。这是首次研究 LRP4/5/6(肌肉骨骼生物学中的关键受体)如何对力学刺激作出反应。对该机制的进一步阐明可能为确定维持软骨健康的药物靶点提供重要的临床益处。