Department of Orthopaedic.Surgery, Lovisenberg Deaconal.Hospital, Oslo, Norway.
Br J Sports Med. 2011 Oct;45(13):1035-9. doi: 10.1136/bjsm.2010.083188. Epub 2011 Apr 10.
Little information exists on the contribution of apoptosis to pathological tendon changes in rotator cuff tendinopathy. The purpose of this study was to quantitate the rate of tenocyte apoptosis in torn supraspinatus tendons and in the matched intact subscapularis and to examine the potential relation between apoptotic index (AI) and tendon pathology. In addition, the authors examined tenocyte density, proliferation rate and p53 gene expression patterns to gain further insight into relevant pathological mechanisms in the torn suprapinatus. 15 torn supraspinatus tendons with matched intact subscapularis tendon samples and 10 reference subscapularis samples were collected. Immunohistochemistry was used to define the AI (F7-26), proliferation rate (Ki67) and presence of p53 (M7001). Tendon degeneration was evaluated according to the Bonar scale. Expression of p53 and relevant genes (n=84) was examined on a subset of samples using microfluidic arrays. The AI was significantly increased in torn supraspinatus tendon and matched subscapularis tendon (R² =0.5742; p=0.0005). Cell density and proliferation rate were also elevated in torn supraspinatus compared with reference subscapularis tendons (p<0.05). A significant increase in p53 occurred specifically in torn supraspinatus tendon (p<0.05), and several genes encoding p53-inhibiting proteins were downregulated in association, including HDAC1 (p<0.05), MDM4 (p<0.001) and PPM1D (p<0.05). Our results suggest that tenocyte apoptosis results from more than one mechanism in the injured rotator cuff, including both intrinsic factors related specifically to the torn supraspinatus tendon, as well as a more generalised effect on the adjacent subscapularis tendon.
关于细胞凋亡在肩袖肌腱病的病理变化中的作用,目前相关信息较少。本研究旨在定量测定撕裂的冈上肌腱中的成纤维细胞凋亡率,并与匹配的完整肩胛下肌腱进行比较,同时检测凋亡指数(AI)与肌腱病理之间的潜在关系。此外,作者还检测了成纤维细胞密度、增殖率和 p53 基因表达模式,以进一步深入了解撕裂的冈上肌腱中的相关病理机制。收集了 15 例撕裂的冈上肌腱和 10 例匹配的肩胛下肌腱以及 10 例参考肩胛下肌腱样本。免疫组织化学用于定义 AI(F7-26)、增殖率(Ki67)和 p53 的存在(M7001)。根据 Bonar 量表评估肌腱退变。使用微流控芯片在部分样本中检测了 p53 及其相关基因(n=84)的表达。与匹配的肩胛下肌腱相比,撕裂的冈上肌腱和肩胛下肌腱中的 AI 显著增加(R²=0.5742;p=0.0005)。与参考肩胛下肌腱相比,撕裂的冈上肌腱中成纤维细胞密度和增殖率也升高(p<0.05)。p53 的表达仅在撕裂的冈上肌腱中显著增加(p<0.05),并且几个编码 p53 抑制蛋白的基因下调,包括 HDAC1(p<0.05)、MDM4(p<0.001)和 PPM1D(p<0.05)。我们的结果表明,冈上肌腱损伤后的成纤维细胞凋亡是多种机制共同作用的结果,包括与撕裂的冈上肌腱特异性相关的内在因素,以及对相邻肩胛下肌腱的更普遍影响。