收稿日期: 2020-10-12
网络出版日期: 2021-02-07
Expression of cartilage oligomeric matrix protein in the synovial chondromatosis of the temporomandibular joint
Received date: 2020-10-12
Online published: 2021-02-07
目的: 检测软骨寡聚基质蛋白(cartilage oligomeric matrix protein,COMP)在颞下颌关节滑膜软骨瘤病(synovial chondromatosis of the temporomandibular joint,TMJSC)中的表达,并初步探讨其在TMJSC发病中可能的作用。方法: 选取2011年1月至2020年2月于北京大学口腔医院就诊的有完整病历资料、经手术治疗且术后病理诊断为TMJSC的患者,通过免疫组织化学实验、蛋白免疫印记法及实时荧光定量PCR,分别在蛋白、mRNA水平检测TMJSC中COMP、转化生长因子(transforming growth factor,TGF)-β3、TGF-β1、骨形态发生蛋白-2(bone morphogenetic protein-2,BMP-2)等细胞因子的表达情况,并与正常滑膜组织进行比较。显微镜下观察病变的组织形态学特征、蛋白表达及分布情况,对阳性染色蛋白进行半定量分析;采用SPSS 22.0统计软件对实验结果进行分析,P<0.05表示差异有统计学意义。结果: 免疫组织化学实验结果显示,TMJSC组织中COMP阳性表达多见于滑膜组织及与滑膜邻近的软骨细胞内,与正常滑膜组织相比表达明显增多;TMJSC复发病例中COMP阳性表达评分较未复发病例更高;TGF-β3、TGF-β1及BMP-2阳性表达分布与COMP类似,表达水平较正常滑膜组织明显增高;该结论在蛋白免疫印迹法中得到进一步印证。实时荧光定量PCR检测结果显示,COMP、TGF-β3、TGF-β1及BMP-2的表达较正常滑膜组织均有增高。结论: COMP在TMJSC中表达显著增高,并与TGF-β3、TGF-β1及BMP-2间存在协同作用,可能在该肿瘤的发病中起一定作用。
韩玮华 , 罗海燕 , 郭传瑸 , 宁琦 , 孟娟红 . 软骨寡聚基质蛋白在颞下颌关节滑膜软骨瘤病中的表达[J]. 北京大学学报(医学版), 2021 , 53(1) : 34 -39 . DOI: 10.19723/j.issn.1671-167X.2021.01.006
Objective: To detect the expression of cartilage oligomeric matrix protein (COMP) in the synovial chondromatosis of the temporomandibular joint (TMJSC),and to discuss the possible interactions between COMP, transforming growth factor (TGF)-β3, TGF-β1 and bone morphogenetic protein-2 (BMP-2) in the development of this neoplastic disease.Methods: Patients in Peking University School and Hospital of Stomatology from January 2011 to February 2020 were selected, who had complete medical records, TMJSC was verified histologically after operation. The expressions of COMP, TGF-β3, TGF-β1 and BMP-2 in the TMJSC of the temporomandibular joint were detected by immunohistochemistry and quantitative real-time PCR (RT-PCR) at the protein level and mRNA level respectively, compared with the normal synovial tissue of temporomandibular joint. The histological morphology, protein expression and distribution of TMJSC tissues were observed microscopically, and the positive staining proteins were counted and scored. SPSS 22.0 statistical software was used to analyze the expression differences between the related proteins in TMJSC tissue and the normal synovial tissue of temporomandibular joint and to compare their differences. P<0.05 indicated that the difference was statistically significant.Results: Immunohistochemical results showed that the positive expression of COMP in TMJSC tissues was mostly found in synovial tissues and chondrocytes adjacent to synovial tissues, and the difference was statistically significant, compared with the normal temporomandibular joint synovial tissues. The positive expression of COMP was significantly different between recurrent TMJSC and non-recurrent ones. The positive expressions of TGF-β3, TGF-β1 and BMP-2 were higher than the normal synovial tissue, and were also mostly found in the synovial cells and adjacent chondrocytes, which was further confirmed by Western blot. According to the RT-PCR results, the expressions of COMP, TGF-β3, TGF-β1 and BMP-2 in TMJSC were higher than those in the normal synovial tissue.Conclusion: The expression of COMP in TMJSC of temporomandibular joint increased significantly, compared with the normal synovial tissue. There may be interactions between COMP and cytokines related to the proliferation and differentiation, like TGF-β3, TGF-β1 and BMP-2, which may play a potential role in the pathogenesis of TMJSC.
| [1] | Meng JH, Guo CB, Yi B, et al. Clinical and radiologic findings of synovial chondromatosis affecting the temporomandibular joint[J]. Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 2010,109(3):441-448. |
| [2] | Coles MJ, Tara HH. Synovial chondromatosis: a case study and brief review[J]. Am J Orthop (Belle Mead NJ), 1997,26(1):37-40. |
| [3] | 韩方凯, 马绪臣. 颞下颌关节滑膜软骨瘤病[J]. 现代口腔医学杂志, 2006,20(4):425-428. |
| [4] | Helmy ES, Bays RA, Sharawy MM. Synovial chondromatosis associated with experimental osteoarthritis in adult monkeys[J]. J Oral Maxillofac Surg, 1989,47(8):823-827. |
| [5] | Li YJ, Cai HX, Fang W, et al. Fibroblast growth factor 2 involved in the pathogenesis of synovial chondromatosis of temporomandibular joint[J]. J Oral Pathol Med, 2014,43(5):388-394. |
| [6] | Li Y, El Mozen LA, Cai H, et al. Transforming growth factor beta 3 involved in the pathogenesis of synovial chondromatosis of temporomandibular joint[J]. Sci Rep, 2015,5:8843. |
| [7] | Sandberg MM, Aro HT, Vuorio EI. Gene expression during bone repair[J]. Clin Orthop and Relat Res, 1993(289):292-312. |
| [8] | Nishimura K, Solchaga LA, Caplan AI, et al. Chondroprogenitor cells of synovial tissue[J]. Arthritis Rheum, 2010,42(12):2631-2637. |
| [9] | Pearson CA, Pearson D, Shibahara S, et al. Tenascin: cDNA cloning and induction by TGF-beta[J]. EMBO J, 1988,7(10):2977-2982. |
| [10] | Mackie EJ, Thesleff I, Chiquet-Ehrismann R. Tenascin is asso-ciated with chondrogenic and osteogenic differentiation in vivo and promotes chondrogenesis in vitro[J]. J Cell Biol, 1987,105(6):2569-2579. |
| [11] | Nakanishi S, Sskamoto K, Yoshitake H, et al. Bone morphoge-netic proteins are involved in the pathobiology of synovial chondromatosis[J]. Biochem Biophys Res Commun, 2009,379(4):914-919. |
| [12] | Iwata H, Ono S, Sato K, et al. Bone morphogenetic protein-induced muscle- and synovium-derived cartilage differentiation in vitro[J]. Clin Orthop Relat Res, 1993(296):295-300. |
| [13] | Wang C, Liu G, Zhang W, et al. Cartilage oligomeric matrix protein improves in vivo cartilage regeneration and compression modulus by enhancing matrix assembly and synjournal[J]. Colloids Surf B Biointerfaces, 2017,159:518-526. |
| [14] | Zaucke F, Dinser R, Maurer P, et al. Cartilage oligomeric matrix protein (COMP) and collagen Ⅸ are sensitive markers for the differentiation state of articular primary chondrocytes[J]. Biochem J, 2001,358(1):17-24. |
| [15] | 游洪波, 陈安民, 王国宾, 等. 转化生长因子-β诱导前软骨干细胞成软骨分化的研究[J]. 中华创伤杂志, 2010,26(5):453-459. |
| [16] | Li H, Haudenschild DR, Posey KL, et al. Comparative analysis with collagen type Ⅱ distinguishes cartilage oligomeric matrix protein as a primary TGFβ-responsive gene[J]. Osteoarthritis Cartilage, 2011,19(10):1246-1253. |
| [17] | Haudenschild DR, Hong E, Yik JH, et al. Enhanced activity of transforming growth factor-β1 (TGF-β1) bound to cartilage oligomeric matrix protein[J]. J Biol Chem, 2011,286(50):43250-43258. |
| [18] | Guo P, Shi Z L, Liu A, et al. Effects of cartilage oligomeric matrix protein on bone morphogenetic protein-2-induced differen-tiation of mesenchymal stem cells[J]. Orthop Surg, 2015,6(4):280-287. |
| [19] | 于萍, 步宏, 王华, 等. 免疫组化结果的图像分析与人工计数方法的对比研究[J]. 生物医学工程学杂志, 2003,20(2):288-290. |
| [20] | Ardekian L, Faquin W, Troulis MJ, et al. Synovial chondromatosis of the temporomandibular joint: report and analysis of eleven cases[J]. J Oral Maxillofac Surg, 2005,63(7):941-947. |
| [21] | Fujita S, Iizuka T, Tuboi Y, et al. Synovial chondromatosis of the temporomandibular joint with immunohistochemical findings: Report of a case[J]. J Oral Maxillofac Surg, 1991,49(8):880-883. |
| [22] | Hedbom E, Antonsson P, Hjerpe A, et al. Cartilage matrix proteins: An acidic oligomeric protein (COMP) detected only in cartilage[J]. J Biol Chem, 1992,267(9):6132-6136. |
| [23] | Recklies AD, Baillargeon L, White C. Regulation of cartilage oligomeric matrix protein synjournal in human synovial cells and arti-cular chondrocytes[J]. Arthritis Rheum, 1998,41(6):997-1006. |
| [24] | Andersson ML, Thorstensson CA, Roos EM, et al. Serum levels of cartilage oligomeric matrix protein (COMP) increase temporarily after physical exercise in patients with knee osteoarthritis[J]. BMC Musculoskelet Disord, 2006,7:98. |
| [25] | Chen HC, Shah SH, Li YJ, et al. Inverse association of general joint hypermobility with hand and knee osteoarthritis and serum cartilage oligomeric matrix protein levels[J]. Arthritis Rheum, 2008,58(12):3854-3864. |
| [26] | Blumbach K, Bastiaansen-Jenniskens YM, DeGroot J, et al. Combined role of type Ⅸ collagen and cartilage oligomeric matrix protein in cartilage matrix assembly: Cartilage oligomeric matrix protein counteracts type Ⅸ collagen-induced limitation of cartilage collagen fibril growth in mouse chondrocyte cultures[J]. Arthritis Rheum, 2009,60(12):3676-3685. |
| [27] | Nozawa-Inoue K, Amizuka N, Ikeda N, et al. Synovial membrane in the temporomandibular joint: Its morphology, function and development[J]. Arch Histol Cytol, 2003,66(4):289-306. |
| [28] | 路红艳, 李健, 龙星. 间充质干细胞表面标记在颞下颌关节疾病患者滑膜间充质细胞表达的比较[J]. 口腔医学研究, 2018,34(11):1249-1252. |
| [29] | 符培亮, 丛锐军, 张雷, 等. 体外条件下TGF-β3、BMP-2和DEX诱导兔滑膜间充质干细胞向软骨细胞谱系分化的研究[J]. 中国骨与关节杂志, 2014(2):135-141. |
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