Hindle Paul, Hall Andrew C, Biant Leela C
Department of Trauma and Orthopaedic Surgery, The Royal Infirmary of Edinburgh, Edinburgh, The United Kingdom; Centre for Integrative Physiology, School of Biomedical Sciences, The University of Edinburgh, Edinburgh, Edinburgh, The United Kingdom.
J Orthop Res. 2014 Nov;32(11):1495-502. doi: 10.1002/jor.22701. Epub 2014 Aug 2.
Cell viability is crucial for effective cell-based cartilage repair. The aim of this study was to determine the effect of handling the membrane during matrix-induced autologous chondrocyte implantation surgery on the viability of implanted chondrocytes. Images were acquired under five conditions: (i) Pre-operative; (ii) Handled during surgery; (iii) Cut edge; (iv) Thumb pressure applied; (v) Heavily grasped with forceps. Live and dead cell stains were used. Images were obtained for cell counting and morphology. Mean cell density was 6.60 × 10(5) cells/cm(2) (5.74-7.11 × 10(5) ) in specimens that did not have significant trauma decreasing significantly in specimens that had been grasped with forceps (p < 0.001) or cut (p = 0.004). Cell viability on delivery grade membrane was 75.1%(72.4-77.8%). This dropped to 67.4%(64.1-69.7%) after handling (p = 0.002), 56.3%(51.5-61.6%) after being thumbed (p < 0.001) and 28.8%(24.7-31.2%) after crushing with forceps (p < 0.001). When cut with scissors there was a band of cell death approximately 275 µm in width where cell viability decreased to 13.7%(10.2-18.2%, p < 0.001). Higher magnification revealed cells without the typical rounded appearance of chondrocytes. We found that confocal laser-scanning microscope (CLSM) can be used to quantify and image the fine morphology of cells on a matrix-induced autologous chondrocyte implantation (MACI) membrane. Careful handling of the membrane is essential to minimise chondrocyte death during surgery.
细胞活力对于基于细胞的有效软骨修复至关重要。本研究的目的是确定在基质诱导的自体软骨细胞植入手术过程中处理膜对植入软骨细胞活力的影响。在五种条件下采集图像:(i)术前;(ii)手术中处理;(iii)切缘;(iv)施加拇指压力;(v)用镊子大力抓取。使用活细胞和死细胞染色剂。获取图像用于细胞计数和形态观察。在没有明显创伤的标本中,平均细胞密度为6.60×10⁵个细胞/cm²(5.74 - 7.11×10⁵),在用镊子抓取(p < 0.001)或切割(p = 0.004)的标本中显著降低。递送级膜上的细胞活力为75.1%(72.4 - 77.8%)。处理后降至67.4%(64.1 - 69.7%,p = 0.002),拇指按压后降至56.3%(51.5 - 61.6%,p < 0.001),用镊子挤压后降至28.8%(24.7 - 31.2%,p < 0.001)。用剪刀切割时,有一条宽度约为275 µm的细胞死亡带,此处细胞活力降至13.7%(10.2 - 18.2%,p < 0.001)。更高倍率显示细胞没有软骨细胞典型的圆形外观。我们发现共聚焦激光扫描显微镜(CLSM)可用于量化和成像基质诱导的自体软骨细胞植入(MACI)膜上细胞的精细形态。手术过程中小心处理膜对于将软骨细胞死亡降至最低至关重要。