Orthopaedic Institute, Department of Orthopaedics, The First Affiliated Hospital, Soochow University, Suzhou, Jiangsu, China.
Spine (Phila Pa 1976). 2017 Oct 1;42(19):E1104-E1111. doi: 10.1097/BRS.0000000000002085.
In vitro study using rat intervertebral discs (IVDs).
To explore the alteration of annulus fibrosus collagen fibrils after loading on IVD and to investigate the degeneration pathogenesis at the nanoscale.
Abnormal loading can lead to IVD degeneration, but the precise mechanism has been hitherto elusive, especially at the nanoscale.
A rat IVD loading model was used, which combined bending of the tail by 40° with compressive loading of 1.8, 4.5, and 7.2 N of the rat tail using an external fixation device. The structure and the elastic modulus of individual collagen fibrils within IVD Co8-Co9 was examined 2 weeks after loading at the nanoscale using atomic force microscopy.
Significant fibril disorder and a decrease in cell number within the annulus fibrosus after loading was observed at the microscale as judged by hematoxylin/eosin staining, suggesting initiation of rupture of the structure and degradation of the IVD. The annulus fibrosus collagen fibrils underwent a change in diameter and elastic modulus from 170 ± 18 to 310 ± 24 nm (P < 0.001) and 0.86 ± 0.12 to 1.27 ± 0.30 GPa (P = 0.003), respectively when measured on the concave side after a loading of 7.2 N. Thus the loading process resulted in a thickening and stiffening of collagen fibrils with a difference between the inner and outer layers.
The results of the present study indicated that abnormal loading was not only associated with disorder at the microscale, but also alteration of the collagen fibrils at the nanoscale, possibly leading to changes in the mechanical and physiological environment around the cells of the annulus fibrosus.
N/A.
使用大鼠椎间盘进行体外研究。
探索椎间盘纤维环胶原纤维在受力后的变化,并在纳米尺度上研究其退变的发病机制。
异常负荷可导致椎间盘退变,但确切机制迄今仍不清楚,特别是在纳米尺度上。
使用一种大鼠椎间盘加载模型,该模型将大鼠尾部弯曲 40°与尾部施加 1.8、4.5 和 7.2 N 的压缩载荷相结合,使用外部固定装置。在加载后 2 周,使用原子力显微镜在纳米尺度上检查椎间盘 Co8-Co9 内单个胶原纤维的结构和弹性模量。
苏木精/伊红染色显示,微尺度上纤维环的纤维排列紊乱,细胞数量减少,提示结构破裂和椎间盘降解的开始。纤维环胶原纤维的直径和弹性模量分别从 170±18nm 变为 310±24nm(P<0.001)和 0.86±0.12GPa 变为 1.27±0.30GPa(P=0.003),当在 7.2N 加载时在凹侧测量。因此,加载过程导致胶原纤维变厚和变硬,内外层之间存在差异。
本研究结果表明,异常负荷不仅与微尺度上的紊乱有关,而且与胶原纤维在纳米尺度上的改变有关,这可能导致纤维环细胞周围的机械和生理环境发生变化。
无。