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MMP-13和Galectin-3在骨性关节炎滑膜组织中的临床意义 被引量:9

The clinical significance of Matrix Metalloproteinase-13 and Galectin-3 in synovial tissues of osteoarthritis
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摘要 目的检测MMP-13和Galectin-3在骨性关节炎滑膜组织中的表达,探讨二者在骨性关节炎发病机制中的作用。方法通过关节镜获取42例骨性关节炎滑膜标本,同时选择12例非正常死亡及外伤性截肢的健康青年的滑膜组织作为对照组。采用免疫组化检测MMP-13及Galectin-3在骨性关节炎滑膜组织中的表达。结果病理观察显示骨性关节炎滑膜细胞增生,淋巴细胞及浆细胞浸润,甚至形成淋巴滤泡,同时微血管增生,管壁增厚。免疫组化结果显示:在骨性关节炎滑膜组织中,MMP-13蛋白主要表达于滑膜衬里层细胞、炎细胞、巨噬细胞样组织细胞以及少许血管内皮细胞。在正常滑膜组织中,MMP-13蛋白则主要表达于滑膜衬里层细胞。二者的阳性细胞率分别为0.387±0.042和0.053±0.019,前者的阳性表达率明显高于后者(P<0.05)。Galectin-3蛋白在骨性关节炎组中的阳性表达主要分布于滑膜衬里层细胞及滑膜下层少许炎细胞中。Galectin-3蛋白在骨性关节炎组和对照组的阳性细胞率分别为0.267±0.044和0.046±0.021。前者的阳性表达率明显高于后者(P<0.05)。MMP-13和Galectin-3在骨性关节炎滑膜中表达与患者年龄及性别无关(P>0.05),而与骨性关节炎X线片临床分期有关,MMP-3与Galectin-3在滑膜中的表达均随着骨性关节炎X线片临床分期的增高而增强(P<0.05)。结论 MMP-13蛋白和Galectin-3蛋白在骨性关节炎滑膜组织中的表达显著高于正常滑膜组织,随X线片临床分期的增高而增强,表明二者参与骨性关节炎滑膜的病理过程,对滑膜炎起相互促进作用,临床检测滑膜组织中MMP-13蛋白和Galectin-3蛋白的表达有助于指导骨性关节炎的治疗及病情的评估。 Objective To detect the protein expressions of Matrix Metalloproteinase-13 ( MMP-13 ) and Galectin-3 in synovial tissues of osteoarthritis, and to explore their effects in the pathogenesis of osteoarthritis. Methods 42 cases of synovial specimens of osteoarthritis and 12 cases of synovial tissues from healthy young adults who died of unnatural causes or traumatic amputation ( the control group ) were obtained by arthroscopy. The protein expressions of MMP-13 and Galectin-3 in synovial tissues of osteoarthritis were detected by immunohistochemistry. Results Pathological observation showed the synovial cell hyperplasia of osteoarthritis, infiltration of lymphocytes and plasma cells, formation of lymphoid follicles, micrangium hyperplasy and pipe wall thinkening. Immunohistochemistry results showed in synovial tissues of osteoarthritis the MMP-13 protein expression mainly appeared in synovial lining layer cells, inflammatory cells, macrophages and few endothelial cells, whereas in normal synovial tissues the MMP- 13 protein expression mainly appeared in synovial lining layer cells. The positive cell rates of MMP-13 in synovial tissues of osteoarthritis and in normal synovial tissues were 0.387i0.042 and 0.053:k0.019 respectively. The positive expression rate of MMP-13 in synovial tissues of osteoarthritis was obviously higher than that in normal synovial tissues ( P〈0.05 ). The positive expression of Galectin-3 protein in the osteoarthritis group mainly appeared in synovial lining layer cells and few inflammatory cells in the synoviale subintima. The positive cell rates of Galectin-3 protein in the osteoarthritis group and control group were 0.267±0.044 and 0.046+0.021 respectively. The positive expression rate of Galectin-3 protein in the osteoarthritis group was obviously higher than that in the control group ( P〈0.05 ).The protein expressions of MMP-13 and Galectin-3 in synovial tissues of osteoarthritis were not related with the age and gender of patients ( P〉0.05 ), but were related to the osteoarthritis X-ray clinical staging. The protein expressions of MMP-13 and Galectin-3 in synovial tissues became evident with the increase of the osteoarthritis X-ray clinical staging (P〈0.05). Conclusions The expressions of MMP-13 protein and Galectin-3 protein in synovial tissues of osteoarthritis are significantly higher than that in normal synovial tissues, which becomes evident with the increase of the X-ray clinical staging. The findings suggest that they both participate in the pathological process of synovial tissues of osteoarthritis and promote their mutual effects on synovitis. So that, they contribute to treating and assessing the condition of osteoarthritis by clinically detecting the expressions of the MMP-13 protein and Galectin-3 protein in synovial tissues.
出处 《中国骨与关节杂志》 CAS 2013年第5期280-284,共5页 Chinese Journal of Bone and Joint
关键词 骨关节炎 滑膜 基质金属蛋白酶13 半乳糖凝集素3 Osteoarthritis Synovial Membrane Matrix metalloproteinase 13 Galectin 3
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参考文献19

  • 1Singer I,Kawka DW,Scott S. The relation of matrixmetallo- proteinase and human osteoarthritis[J].{H}ARTHRITIS AND RHEUMATISM,2003,(09):2642-2648.
  • 2Milner JM,Patel A,Davidson RK. Matriptase is a novel initiator of cartilage matrix degradation in osteoarthritis[J].{H}ARTHRITIS AND RHEUMATISM,2010,(07):1955-1966.
  • 3Goldring MB,Otero M,Plumb DA. Roles of inflammatory and anabolic cytokines in cartilage metabolism:signals and multiple effectors converge upon MMP-13 regulation in osteoarthritis[J].Eur Cell Mater,2011.202-220.
  • 4Freemont AJ,Hampson V,Tilman R,et a1. Gene expression of matrix metalloproteinases 1,3,and 9 by chondrocytes in osteoarthritic human knee articular cartilage is zone and grade specific[J].{H}ANNALS OF THE RHEUMATIC DISEASES,1997,(09):542-549.
  • 5Imai K,Ohta S,Matsumoto T,et a1. Expression of membrane-b type 1 matrix metalloproteinase and activation of progelatinase A in human osteoarthritic cartilage[J].{H}AMERICAN JOURNAL OF PATHOLOGY,1997,(01):245-256.
  • 6Balkman CE,Nixon AJ. Molecular cloning and cartilage gene expression of equine stromelysin 1(matrix metalloproteinase 3)[J].{H}American Journal of Veterinary Research,2008,(01):30-36.
  • 7Anderson DC,Izzo MW,Hall DJ,et a1. Comparative gene expression profiling of normal anddegenerative discs:analysis of a rabbit annular laceration model[J].{H}SPINE,2002,(12):1291-1296.
  • 8Roberts S,Caterson B,Menage J,et a1. Matrix metallopro-teinases and aggrecanase:their role in disorders of the human intervertebral disc[J].{H}SPINE,2000,(23):3005-3013.
  • 9Wernicke D,Schulze-Westhoff C,Brauer R. Stimulation of collagenase3 expression in synovial fibroblasts of patients with rheumatoid arthritis by contact with a three-dimensional collagenmatrix or with normal cartilage when coimplanted in NOD/SCIDmice[J].{H}ARTHRITIS AND RHEUMATISM,2002,(01):64-74.
  • 10Li NG,Shi ZH,Tang YP. New hope for the treatment of osteoarthritis through selective inhibition of MMP-13[J].{H}Current Medicinal Chemistry,2011,(07):977-1001.

二级参考文献15

  • 1张超,王旭,姜建元,黄煌渊.MMP-1、13 mRNA和DDR2表达与关节软骨退变的关系[J].复旦学报(医学版),2007,34(1):126-128. 被引量:27
  • 2Mort JS, Billington CJ.Articular cartilage and changes in arthritis matrix degradation[J].Arthritis Res, 2001,3 : 337-341.
  • 3Murphy G,Knauper V.Matrix metaIloproteinases in arthritic dise- ase[J].Arthritis Res,2002,4(Suppl 3):39-49.
  • 4Pelletier JP,Jovanovie D,Fernandes JC,et al.Reduced progression of experimental osteoarthritis in vivo by selective inhibition of inducible nitric oxide synthase [J].Arthritis Rheum, 1998,41 (7): 1275-1286.
  • 5Mankin HJ, Dorfman H, Lippiello L, et al. Biochemical and metabolic abnormalities in articular cartilage from osteoarthritic human hips: II.correIation of morphology with biochemical and metabolic data. J Bone Joint Surg Am,1971,53: 523-537.
  • 6Reddi AH.Aging,osteoarthritis and transforming growth factorbeta signaling in cartilage.Arthritis Res Ther,2006,8:101.
  • 7Peter JB,Rosa S.Mechanical propertiers of the collagen network in human articular cartilage as measured by osomotic stress techuioueH1.Arch Bioch & Biooh. 1998.351 (2) : 207.
  • 8Stoop R,Buma P,Vander Kraan PM,et al.Type Ⅱ collagen degradation in articular cartilage fibrillation after anterior cruciate ligment transection in rats[J].Osteoarthr Cartil, 2001,9(4) : 308-315.
  • 9Peter JB,Rosa S.Mechanical propertiers of the collagen network in human articular cartilage as measured by osomotic stress technique[J].Arch Bioch & Bioph,1998;351(2):207
  • 10Kleiner DE,Steler-Stevenson WG.Structural biochemistry and activation of matrix metalloproteinase[J].Curr Opin Cell Boil,1993,5:891

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同被引文献90

  • 1刘献祥,李西海,周江涛.改良Hulth造模法复制膝骨性关节炎的实验研究[J].中国中西医结合杂志,2005,25(12):1104-1108. 被引量:128
  • 2富丽萍,王绍武,宋清伟,康健蕴,王福生,王立德.软骨的MR敏感序列在软骨类病变中的应用研究[J].中国CT和MRI杂志,2007,5(4):12-17. 被引量:4
  • 3Rabquer B J, Tan G J, Shaheen P J ,et al. Synovial inflammation in patients with osteonecrosis of the femoral head [J]. Clin Transl Sci, 2009, 2(4) :273 -8.
  • 4Takaishi H, Kimm T ,Dalai S, et al. Joint diseases and matrix metalloproteinases , a role for rMMP-13 [J]. Curt Pham Biotechnol, 2008, 9(1) :47 -54.
  • 5Berenbaum F. Osteoarthritis as an inflammatory disease (osteoarthritis is not osteoarthrosis l)[J]. Osteoarthritis Cartilage, 2013, 21(1):16-21.
  • 6Goldring M B, Otero M, Plumb D A, et al. Roles of inflammatory and anabolic cytokines in cartilage metabolism: signals and multiple effectors converge upon MMP -13 regulation in osteoarthritis [J]. European Cells Material, 2011 , 21 :202 - 20.
  • 7Koskinen A, Vuolteenaho K, Nieminen R,et al. Leptin enhances MMP-l, MMP-3 and MMP-13 production in human osteoarthritic cartilage and correlates with MMP-1 and MMP-3 in synovial fluid from OA patients [J]. Clin Exp Rheumatol, 2011 , 29 ( 1): 57 - 64.
  • 8Sokolove J, Lepus C M. Role of inflammation in the pathogenesis of osteoarthritis: latest findings and interpretations [J]. Ther Adv Musculoskelet Dis, 2013, 5(2):77 -94.
  • 9Arnalinei C, Caruntu I D, Giusca S E, et al. Matrix metalloproteinases involvement in pathologic conditions [J]. Rom J Morphol Embryol, 2010, 51(2) :215 -28.
  • 10Hashimoto M,Nakasa T,Hikata T,et al.Molecular net- work of cartilage homeostasis and osteoarthritis [J] . Med Res Rev,2008,28 ( 3 ) :464-481.

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