Kohno H, Shigeno C, Kasai R, Akiyama H, Iida H, Tsuboyama T, Sato K, Konishi J, Nakamura T
Department of Orthopaedic Surgery, Graduate School of Medicine, Kyoto University, Sakyo, Japan.
J Bone Miner Res. 1997 May;12(5):847-54. doi: 10.1359/jbmr.1997.12.5.847.
High levels of immunoreactive and biologically active parathyroid hormone-related peptide (PTHrP) were detected in synovial fluids from patients with osteoarthritis (OA) and rheumatoid arthritis (RA). The levels of PTHrP immunoreactivity in synovial fluids, measured by a two-site immunoradiometric assay (IRMA) which detects hPTHrP(1-72) or longer peptides and a radioimmunoassay (RIA) specific to the carboxy-terminal portion of hPTHrP, were 3.2 +/- 0.3 pmol of hPTHrP(1-86)/l and 61 +/- 7.0 pmol of hPTHrP(109-141)/l in OA patients (mean +/- SE, n = 23), and 4.8 +/- 0.8 pmol of hPTHrP(1-86)/l and 164 +/- 30 pmol of hPTHrP(109-141)/l in RA patients (n = 26). Synovial fluid PTHrP levels distributed above the normal plasma reference ranges in each assay (0.7-2.6 pmol of hPTHrP(1-86)/l; 16-60.6 pmol of hPTHrP(109-141)/l). After concentration using sequential cation-exchange and reverse-phase chromatography, synovial fluid exhibited the activity that stimulated cyclic adenosine monophosphate (cAMP) accumulation in osteoblastic ROS 17/2.8 cells expressing PTH/PTHrP receptors. The cAMP accumulation activity in synovial fluid was sensitive to coincubation with excess hPTHrP(3-40), a PTH/PTHrP receptor antagonist, and was completely neutralized by preincubation with a monoclonal antibody specific to hPTHrP but not PTH. Immunohistochemical analysis of RA synovium revealed that PTHrP was localized in fibroblast-like cells in the synovial pannus invading articular cartilage. Our data show that PTHrP is produced locally by the diseased synovial tissue and released into synovial fluid at high concentrations, allowing us to hypothesize that PTHrP plays a novel role as a paracrine/autocrine factor in the pathology of OA and RA.
在骨关节炎(OA)和类风湿关节炎(RA)患者的滑液中检测到高水平的免疫反应性和生物活性甲状旁腺激素相关肽(PTHrP)。通过检测hPTHrP(1 - 72)或更长肽段的双位点免疫放射分析(IRMA)以及对hPTHrP羧基末端部分特异的放射免疫分析(RIA)测量,OA患者(平均±标准误,n = 23)滑液中PTHrP免疫反应性水平分别为3.2±0.3 pmol hPTHrP(1 - 86)/L和61±7.0 pmol hPTHrP(109 - 141)/L,RA患者(n = 26)分别为4.8±0.8 pmol hPTHrP(1 - 86)/L和164±30 pmol hPTHrP(109 - 141)/L。在每种分析中,滑液PTHrP水平分布在正常血浆参考范围之上(0.7 - 2.6 pmol hPTHrP(1 - 86)/L;16 - 60.6 pmol hPTHrP(109 - 141)/L)。经连续阳离子交换和反相色谱浓缩后,滑液表现出刺激表达PTH/PTHrP受体的成骨细胞ROS 17/2.8细胞中环状单磷酸腺苷(cAMP)积累的活性。滑液中的cAMP积累活性对与过量的hPTHrP(3 - 40)(一种PTH/PTHrP受体拮抗剂)共同孵育敏感,并可通过与特异于hPTHrP而非PTH的单克隆抗体预孵育而完全中和。对RA滑膜的免疫组织化学分析显示,PTHrP定位于侵入关节软骨的滑膜血管翳中的成纤维样细胞。我们的数据表明,PTHrP由病变的滑膜组织局部产生并以高浓度释放到滑液中,这使我们推测PTHrP在OA和RA的病理过程中作为旁分泌/自分泌因子发挥新的作用。