Alhadlaq Hisham A, Xia Yang, Hansen Fay M, Les Clifford M, Lust George
Department of Physics and Center for Biomedical Research, Oakland University, Rochester, Michigan 48309, USA.
Connect Tissue Res. 2007;48(2):76-84. doi: 10.1080/03008200601130950.
We studied the deformation of the extracellular matrices in articular cartilage using a new compression-preservation method in histology. A Hoffman clamp was used to compress the tissue, which remained throughout the paraffin procedure and was removed from the embedded tissue block just before microtoming. Then 14 cartilage-bone blocks from 2 canine humeri were compressed for various strain levels from 5% to 65%. The histological sections were studied using a polarized light microscope, which generated a pair of two-dimensional maps of the fibril orientation (angle) and fibril organization (retardance) for each section. Results were 3-fold. One there was little change in the angle and retardance profiles of the tissue for strain levels 0-15% and a significant change in these profiles for strain levels 15% and above. Two for higher compression, more fibrils became aligned parallel to the articular surface; and three at approximately 30% strain, a second "transitional zone" was formed in the deep part of the tissue. We concluded that this novel compression procedure can be used effectively to study the altered architecture of the collagen matrix in compressed cartilage.
我们使用组织学中的一种新的压缩保存方法研究了关节软骨中细胞外基质的变形。使用霍夫曼夹对组织进行压缩,该夹子在整个石蜡制作过程中一直保留,并且在切片前从包埋的组织块中取出。然后对来自2个犬肱骨的14个软骨 - 骨块进行压缩,应变水平从5%到65%不等。使用偏光显微镜研究组织学切片,该显微镜为每个切片生成一对二维的原纤维取向(角度)和原纤维组织(延迟)图。结果有三方面。其一,对于应变水平0 - 15%,组织的角度和延迟曲线变化很小,而对于应变水平15%及以上,这些曲线有显著变化。其二,对于更高的压缩,更多的原纤维变得与关节表面平行排列;其三,在大约30%应变时,在组织深部形成了第二个“过渡区”。我们得出结论,这种新颖的压缩程序可有效地用于研究压缩软骨中胶原基质的结构变化。