期刊文献+

破骨细胞在强直性脊柱炎滑膜组织中的分化及其在外周关节骨质破坏病理机制中的作用 被引量:7

The differentiation of osteoclast in the synovium and its role in the pathogenesis of peripheral joint bone destruction in ankylosing spondylitis
下载PDF
导出
摘要 目的检测破骨细胞在强直性脊柱炎(AS)外周关节滑膜组织中的分化情况,了解破骨细胞的分化与AS患者外周关节骨质破坏病理改变的相关性。方法应用单克隆抗体,通过免疫组织化学及酶组织化学染色的方法检测13例AS、16例类风湿关节炎(RA)、17例骨关节炎(OA)及6例健康对照关节滑膜组织中CD68蛋白表达及TRAP染色阳性滑膜细胞的分布状况,并通过计算机辅助图像分析系统和半定量分析方法确定CD68分子表达水平及TRAP染色阳性细胞在各研究组滑膜组织中的差异性。结果滑膜组织中均有CD68阳性细胞,AS和RA组CD68表达水平较OA组和健康对照组显著增高(P<0.05),其阳性细胞主要分布于滑膜衬里层,衬里下层也见少量表达;OA和健康者滑膜中仅有少量CD68阳性细胞分布。TRAP染色阳性细胞位于滑膜组织衬里层、淋巴细胞聚集区及滑膜软骨交界区,其中AS组阳性细胞百分数显著低于RA组,OA及正常对照组阳性细胞少见。RA组阳性细胞百分数与RANKL表达水平呈正相关(r=0.442,P=0.043)。结论炎症关节滑膜组织中表达CD68分子及TRAP染色阳性滑膜细胞数量的增加为破骨细胞的分化、成熟提供了充足的细胞数量基础,破骨细胞数量和活性上调是造成强直性脊柱炎外周关节骨质破坏的重要前提。 Objective To compare expression and distribution of CD68 protein and TRAP positive protein in ankylosing spondylitis (AS), rheumatoid arthritis (RA), osteoarthritis (OA), and normal synodal tissues to study the differentiation of osteoclast in synovial tissues obtained from AS patients and its role in the pathogenesis of bone destruction in AS. Methods Immunohistochemical analysis was performed using CD68 monoelonal antibody to detect CD68 expression, and the distribution of TRAP positive cells in the synovial tissues was examined by enzyme histoehernistry in 13 AS, 16 RA, 17 OA patients and 6 healthy controls. The above two variables were quantified in the labeled sections by digital image analysis and semiquantitative analysis to compare the expression of CD68 positive cells in different patient groups and normal subjects. Results Positive CD68 staining was seen in synovial cells from all the patients with AS, RA, OA and normal subjects, and the expression levels of CD68 from patients with AS and RA were higher than those from OA patients and healthy subjects. The CD68 positive cells were abundant mainly in lining layer. In areas where elevated RANKL expression levels were present, the number of TRAP positive cells was found significantly increased in AS and RA synovium. TRAP positive cells were rarely observed in synovium from OA patients and normal controls. There was positive correlation between the number of TRAP positive cells and the RANKL expression (r=0. 442, P=0. 043) in RA patients. Conclusions An obvious increase in the number of CD68 positive cells and TRAP positive cells in synovium may provide a main source of osteoclastogenesis in AS patients. The up-regulation of activity and quantity of osteoclast may have an important role in peripheral articular destruction in patients with AS.
作者 赵伟 黄烽
出处 《解放军医学杂志》 CAS CSCD 北大核心 2005年第11期981-984,共4页 Medical Journal of Chinese People's Liberation Army
基金 国家杰出青年科学基金(编号30025041) 国家自然科学基金(编号A39870720 A30271233)资助课题
关键词 脊柱炎 强直性 关节炎 类风湿 破骨细胞 细胞分化 骨质破坏 spondylitis, ankylosing arthritis, rheumatoid osteoclasts cell differentiation bone destruction
  • 相关文献

参考文献8

  • 1Maksymowych WP. Ankylosing spondylitis-at the interface of bone and cartilage. J Rheumatol, 2000, 27:2295
  • 2Braun J, Bollow M, Sieper J. Radiologic diagnosis and pathology of the spondyloarthropathies. Rheum Dis Clin North Am, 1998, 24:697
  • 3Danks L, Sabokbar A, Gundle R et al. Synovial macrophage-osteoclast differentiation in inflammatory arthritis. Ann Rheum Dis, 2002,61:916
  • 4Fujikawa Y, Shingu M, Torisu T et al. Bone resorption by tartrate-resistant acid phosphatase-positive multinuclear cells isolated from rheumatoid synovium. Br J Rheumatol, 1996, 35:213
  • 5赵伟,黄烽.细胞核因子κB受体活化因子配基在强直性脊柱炎的表达及意义[J].解放军医学杂志,2004,29(6):482-485. 被引量:26
  • 6Udagawa N, Takahashi N, Akatsu T et al. Origin of osteoclasts: mature monocytes and macrophages are capable of differentiating into osteoclasts under a suitable microenvironment prepared by bone marrow-derived stromal cells. Proc Natl Acad Sci USA, 1990, 87:7260
  • 7Takayanagi H, Iizuka H, Juji T et al. involvement of receptor activator of nuclear factor-κB ligand osteoclast differentiation factor in osteoclastogenesis from synoviocytes in rheumatoid arthritis. Arthritis Rheum, 2000, 43:259
  • 8Mori H, Kitazawa R, Mizuki S et al. RANK ligand, RANK, and OPG expression in type II collagen-induced arthritis mouse. Histochem Cell Biol, 2002, 117(3):283

二级参考文献19

  • 1褚洪涛,张百安.云克与松梅乐治疗强直性脊柱炎疗效对比观察[J].中国误诊学杂志,2004,4(3):418-419. 被引量:19
  • 2Gravallese EM, Manning C, Tsay A et al. Synovial tissue in rheumatoid arthritis is a source of osteoclast differentiation factor. Arthritis Rheum, 2000, 43:250
  • 3Kayanagi H, Iizuka H, Juji T et al. Involvement of receptor activator of nuclear factor κB ligand osteoclast differentiation factor in osteoclastogenesis from synoviocytes in rheumatoid arthritis. Arthritis Rheum, 2000, 43:259
  • 4Yukio S, Thomas P, Peter K et al. Expression of osteoclast differentiation factor in rheumatoid arthritis. Arthritis Rheum, 2000, 43: 2523
  • 5Takayanagi H, Iizuka H, Juji T et al. Involvement of receptor activator of nuclear factor κB ligand osteoclast differentiation factor in osteoclastogenesis from synoviocytes in rheumatoid arthritis. Arthritis Rheum, 2000, 43:259
  • 6Toussirot E, Ricard-Blum S, Dumoulin G et al. Relationship between urinary pyridinium cross-links, disease activity and disease subsets of ankylosing spondylitis. Rheumatol (Oxford), 1999, 38:21
  • 7Toussirot E, Michel F, Auge B et al. Bone mass, body composition and bone ultrasound measurements in ankylosing spondylitis. Arthritis Rheum, 1999, 42(suppl): S356
  • 8Amor B, Santos RS, Nahal R et al. Predictive factors for the long term outcome of spondyloarthropathies. J Rheumatol, 1994,21:1883
  • 9Suda T, Takahashi N, Udagawa N et al. Modulation of osteoclast differentiation and function by the new members of the tumor necrosis factor receptor and ligand families. Endocr Rev, 1999, 20:345
  • 10Dayer JM, Bresnihan B. Targeting interleukin-1 in the treatment of rheumatoid arthritis. Arthritis Rheum, 2002, 46:574

共引文献25

同被引文献86

引证文献7

二级引证文献29

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部