Kobayashi K, Mishima H, Hashimoto S, Goomer R S, Harwood F L, Lotz M, Moriya H, Amiel D
Department of Orthopaedics, University of California, San Diego, La Jolla 92093-0630, USA.
J Orthop Res. 2001 Sep;19(5):802-8. doi: 10.1016/S0736-0266(01)00023-7.
Partial medial meniscectomy leads to tibial articular cartilage degeneration. Nitric oxide (NO) production increases with the development of osteoarthritis (OA) and has been shown to have a catabolic effect on chondrocytes. Since distribution of chondrocytic and fibroblastic cell types within the total cell population comprising meniscus is region-specific, we compared NO production in the peripheral and central regions of the medial meniscus 12 weeks after partial medial meniscectomy and assessed chondrocyte apoptosis and NO production in the tibial articular cartilage. Additionally, transcriptional gene expression of inducible nitric oxide synthetase (iNOS) and immunohistochemical staining of nitrotyrosine were examined. The results showed that following partial medial meniscectomy, NO production in the central region of the medial meniscus and in the tibial articular cartilage were significantly higher than respective NO levels in normal and sham-operated controls. Reverse transcription polymerase chain reaction (RT-PCR) revealed a high transcriptional expression of the iNOS gene in the central region of the meniscus and in tibial articular cartilage following partial medial meniscectomy. Nitrotyrosine immunoreactivity was prominent in the central region of the medial meniscus and in the deep layer of the tibial articular cartilage and apoptotic cells were also detected in situ in the superficial zone of the tibial articular cartilage and central regions of the medial meniscus following partial medial meniscectomy. These observations suggest that the central region of the meniscus is responsible for NO synthesis associated with apoptosis in both meniscal and articular cartilage cells following partial meniscectomy.
内侧半月板部分切除术会导致胫骨关节软骨退变。一氧化氮(NO)的产生随着骨关节炎(OA)的发展而增加,并且已被证明对软骨细胞具有分解代谢作用。由于半月板中软骨细胞和成纤维细胞类型在总细胞群体中的分布具有区域特异性,我们比较了内侧半月板部分切除术后12周内侧半月板外周和中央区域的NO产生情况,并评估了胫骨关节软骨中的软骨细胞凋亡和NO产生。此外,还检测了诱导型一氧化氮合酶(iNOS)的转录基因表达和硝基酪氨酸的免疫组织化学染色。结果显示,内侧半月板部分切除术后,内侧半月板中央区域和胫骨关节软骨中的NO产生显著高于正常和假手术对照组各自的NO水平。逆转录聚合酶链反应(RT-PCR)显示,内侧半月板部分切除术后,半月板中央区域和胫骨关节软骨中iNOS基因的转录表达较高。硝基酪氨酸免疫反应在内侧半月板中央区域和胫骨关节软骨深层中较为突出,并且在内侧半月板部分切除术后,在胫骨关节软骨浅表区域和内侧半月板中央区域也原位检测到了凋亡细胞。这些观察结果表明,半月板中央区域在半月板部分切除术后与半月板和关节软骨细胞凋亡相关的NO合成中起作用。