Suzuki Y, Nishikaku F, Nakatuka M, Koga Y
Sumitomo Pharmaceuticals Research Center, Osaka, Japan.
J Rheumatol. 1998 Jun;25(6):1154-60.
To investigate the participation of osteoclast-like bone resorbing cells in the joint destruction of murine collagen induced arthritis (CIA).
After induction of CIA in DBA/1J mice, a histological time course study was conducted on paw sections stained for tartrate resistant acid phosphatase (TRAP), a marker of osteoclasts. Cells from arthritic paws were cultured in vitro with or without indomethacin (IM) or anti-interleukin 6 neutralizing antibody (anti-IL-6), and stained for TRAP. Levels of prostaglandin E2 (PGE2), IL-1beta, IL-6, and tumor necrosis factor-alpha in the culture supernatants were determined by ELISA. The bone resorbing ability of these cells was examined on dentine slices. In control experiments, cells of normal paws or of arthritic tibiae were cultured in the same manner.
TRAP positive osteoclast-like cells were detected late in the development of bone lesions at every eroded front in the pannus-bone and the pannus-subchondral bone junctions of arthritic joints. In vitro, cells of arthritic paws formed bone resorbing osteoclast-like cells spontaneously. However, the control culture failed to form these cells. PGE2 and IL-6 were detected at higher levels in arthritic culture than in control culture. Although both indomethacin and anti-IL-6 reduced osteoclast-like cell formation and indomethacin inhibited PGE2 synthesis, indomethacin failed to reduce IL-6.
These findings suggest the direct participation of osteoclast-like cells in the joint destruction of CIA, the locally enhanced activity of osteoclast-like cell differentiation in arthritic paws, and the participation of prostaglandins and prostaglandin-independent IL-6 in this differentiation.
研究破骨细胞样骨吸收细胞在小鼠胶原诱导性关节炎(CIA)关节破坏中的作用。
在DBA/1J小鼠中诱导CIA后,对用抗酒石酸酸性磷酸酶(TRAP,破骨细胞的标志物)染色的爪部切片进行组织学时间进程研究。将来自关节炎爪部的细胞在有或无吲哚美辛(IM)或抗白细胞介素6中和抗体(抗IL-6)的情况下进行体外培养,并进行TRAP染色。通过酶联免疫吸附测定法测定培养上清液中前列腺素E2(PGE2)、白细胞介素1β、白细胞介素6和肿瘤坏死因子-α的水平。在牙本质切片上检测这些细胞的骨吸收能力。在对照实验中,以相同方式培养正常爪部或关节炎胫骨的细胞。
在关节炎关节的血管翳-骨和血管翳-软骨下骨交界处的每个侵蚀前沿,在骨病变发展后期检测到TRAP阳性破骨细胞样细胞。在体外,关节炎爪部的细胞自发形成骨吸收破骨细胞样细胞。然而,对照培养未能形成这些细胞。在关节炎培养物中检测到的PGE2和IL-6水平高于对照培养物。虽然吲哚美辛和抗IL-6都减少了破骨细胞样细胞的形成,且吲哚美辛抑制PGE2合成,但吲哚美辛未能降低IL-6。
这些发现表明破骨细胞样细胞直接参与CIA的关节破坏,关节炎爪部破骨细胞样细胞分化的局部活性增强,以及前列腺素和不依赖前列腺素的IL-6参与这种分化。