Novakofski K D, Williams R M, Fortier L A, Mohammed H O, Zipfel W R, Bonassar L J
Department of Clinical Sciences, Cornell University, Ithaca, NY, USA.
Department of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.
Osteoarthritis Cartilage. 2014 Feb;22(2):355-62. doi: 10.1016/j.joca.2013.10.008. Epub 2013 Nov 1.
Cartilage injury can lead to post-traumatic osteoarthritis (PTOA). Immediate post-trauma cellular and structural changes are not widely understood. Furthermore, current cellular-resolution cartilage imaging techniques require sectioning of cartilage and/or use of dyes not suitable for patient imaging. In this study, we used multiphoton microscopy (MPM) data with FDA-approved sodium fluorescein to identify and evaluate the pattern of chondrocyte death after traumatic injury.
Mature equine distal metacarpal or metatarsal osteochondral blocks (OCBs) were injured by 30 MPa compressive loading delivered over 1 s. Injured and control sites were imaged unfixed and in situ 1 h post-injury with sodium fluorescein using rasterized z-scanning. MPM data was quantified in MATLAB, reconstructed in 3-D, and projected in 2-D to determine the damage pattern.
MPM images (600 per sample) were reconstructed and analyzed for cell death. The overall distribution of cell death appeared to cluster into circular (n = 7) or elliptical (n = 4) patterns (p = 0.006). Dead cells were prevalent near cracks in the matrix, with only 26.3% (SE = 5.0%, p < 0.0001) of chondrocytes near cracks being viable.
This study demonstrates the first application of MPM for evaluating cellular-scale cartilage injury in situ in live tissue, with clinical potential for detecting early cartilage damage. With this technique, we were able to uniquely observe two death patterns resulting from the same compressive loading, which may be related to local variability in matrix structure. These results also demonstrate proof-of-concept MPM diagnostic use in detecting subtle and early cartilage damage not detectable in any other way.
软骨损伤可导致创伤后骨关节炎(PTOA)。创伤后立即出现的细胞和结构变化尚未得到广泛了解。此外,当前的细胞分辨率软骨成像技术需要对软骨进行切片和/或使用不适合患者成像的染料。在本研究中,我们使用经美国食品药品监督管理局(FDA)批准的荧光素钠的多光子显微镜(MPM)数据来识别和评估创伤性损伤后软骨细胞死亡的模式。
成熟的马远端掌骨或跖骨骨软骨块(OCB)通过在1秒内施加30兆帕的压缩载荷进行损伤。损伤部位和对照部位在损伤后1小时未固定且原位使用荧光素钠进行光栅化z扫描成像。MPM数据在MATLAB中进行量化,进行三维重建,并投影为二维以确定损伤模式。
重建并分析了MPM图像(每个样本600张)中的细胞死亡情况。细胞死亡的总体分布似乎聚集成圆形(n = 7)或椭圆形(n = 4)模式(p = 0.006)。死亡细胞在基质裂缝附近普遍存在,裂缝附近只有26.3%(标准误 = 5.0%,p < 0.0001)的软骨细胞存活。
本研究证明了MPM首次应用于在活组织中原位评估细胞尺度的软骨损伤,具有检测早期软骨损伤的临床潜力。通过这项技术,我们能够独特地观察到由相同压缩载荷导致的两种死亡模式,这可能与基质结构的局部变异性有关。这些结果也证明了MPM在检测以任何其他方式都无法检测到的细微和早期软骨损伤方面的概念验证诊断用途。