Di Cesare P E, Carlson C S, Stollerman E S, Chen F S, Leslie M, Perris R
Musculoskeletal Research Center, Hospital for Joint Diseases Orthopaedic Institute, New York, NY 10003, USA.
FEBS Lett. 1997 Jul 21;412(1):249-52. doi: 10.1016/s0014-5793(97)00789-8.
Human synovium was analyzed for the possible expression of cartilage oligomeric matrix protein (COMP). Immunostaining with polyclonal antiserum to COMP demonstrated positive staining within the synovial cells and immediately subjacent connective tissue, with less intense staining in the deeper connective tissue. Western blot analysis using either polyclonal or monoclonal antibodies to human COMP confirmed the presence of COMP by immunoreactive bands with the same molecular mass (approximately 110 kDa) as purified articular cartilage COMP. PCR using oligonucleotides that span human COMP exons 7-13 revealed identical amplification products from cDNA prepared from either human chondrocytes or synovium. Northern blot analysis using a biotinylated-probe to human COMP, spanning exons 12-13, also reveal an identical hybridization product to either human chondrocyte or synovium total RNA. Human synovium should be considered as a potential tissue source of COMP in any investigation of biological markers of cartilage metabolism.
对人类滑膜组织进行分析,以检测软骨寡聚基质蛋白(COMP)的可能表达情况。用抗COMP多克隆抗血清进行免疫染色显示,滑膜细胞及紧邻的结缔组织呈阳性染色,而深层结缔组织染色较弱。使用抗人COMP的多克隆或单克隆抗体进行的蛋白质印迹分析,通过与纯化关节软骨COMP分子量相同(约110 kDa)的免疫反应条带证实了COMP的存在。使用跨越人COMP外显子7 - 13的寡核苷酸进行PCR,结果显示从人软骨细胞或滑膜制备的cDNA产生相同的扩增产物。使用跨越外显子12 - 13的生物素化人COMP探针进行的Northern印迹分析也显示,人软骨细胞或滑膜总RNA产生相同的杂交产物。在任何关于软骨代谢生物标志物的研究中,人类滑膜都应被视为COMP的潜在组织来源。