Wong Jason, Bennett William, Ferguson Mark W J, McGrouther Duncan A
Faculty of Life Sciences, University of Manchester, UK.
J Anat. 2006 Oct;209(4):533-45. doi: 10.1111/j.1469-7580.2006.00625.x.
Mice are currently the species of choice for the in vivo study of injury, but few detailed anatomical descriptions have been made of rodent digits, limiting their use for the investigation of intrasynovial tendon healing. In this study a detailed microscopic and histological investigation was performed using C57/BL6 and Tie2 LacZ reporter gene transgenic mice. Serial-sectioned mouse hindpaw digits were characterized using haematoxylin and eosin, Masson's trichrome (collagen), Alcian blue (fibrocartilage), Miller's stain (elastin) and TRITC-phalloidin (cellular cytoskeleton) staining. Digital vasculature was demonstrated using FITC-labelled dextran perfusion studies supplemented with LacZ expression in Tie2 LacZ transgenic mice digits. Imaging of the digit used a combination of brightfield and confocal microscopy with three-dimensional reconstruction. Our findings demonstrated that the mouse hindpaw possesses deep and superficial flexor tendons within a synovial sheath comparable with that found in other mammalian species. The intrasynovial tendons were avascular and had regions of fibrocartilaginous specialization relating to areas of compression. Corresponding vascular networks were demonstrated around the sheath using Tie2 LacZ mice and FITC-perfused hindpaws. Furthermore, there is an area of digit where both deep and superficial tendons reside between two pulleys, similar to zone 2 in the human hand where it would be possible to study intrasynovial tendon injury and adhesion formation. In conclusion, although the dimensions of the mouse digit pose technical challenges for surgical intervention, we have identified a model for the study of flexor tendon injury that will permit future genetic manipulation studies.
小鼠目前是体内损伤研究的首选物种,但对啮齿动物指(趾)的详细解剖描述较少,限制了它们在滑膜内肌腱愈合研究中的应用。在本研究中,使用C57/BL6和Tie2 LacZ报告基因转基因小鼠进行了详细的微观和组织学研究。使用苏木精和伊红、马松三色染色法(胶原蛋白)、阿尔辛蓝(纤维软骨)、米勒染色法(弹性蛋白)和TRITC-鬼笔环肽(细胞细胞骨架)染色对连续切片的小鼠后足指(趾)进行表征。通过在Tie2 LacZ转基因小鼠指(趾)中补充LacZ表达的FITC标记葡聚糖灌注研究来显示指(趾)部血管系统。指(趾)成像使用明场和共聚焦显微镜结合三维重建。我们的研究结果表明,小鼠后足在滑膜鞘内具有深、浅屈肌腱,与其他哺乳动物物种中的情况类似。滑膜内肌腱无血管,并且在与受压区域相关的部位具有纤维软骨特化区域。使用Tie2 LacZ小鼠和FITC灌注的后足在滑膜鞘周围显示出相应的血管网络。此外,在指(趾)的一个区域,深、浅肌腱都位于两个滑车之间,类似于人类手部的2区,在该区域有可能研究滑膜内肌腱损伤和粘连形成。总之,尽管小鼠指(趾)的尺寸给手术干预带来了技术挑战,但我们已经确定了一种用于研究屈肌腱损伤的模型,这将允许未来进行基因操作研究。