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首页> 外文期刊>Rheumatology International >Autoimmune reaction to type II collagen and cartilage degeneration in MRL/Mp-lpr/lpr mouse
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Autoimmune reaction to type II collagen and cartilage degeneration in MRL/Mp-lpr/lpr mouse

机译:MRL / Mp-lpr / lpr小鼠对II型胶原的自身免疫反应和软骨变性

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The early phase of cartilage degeneration was immunohistochemically examined in order to clarify the importance of autoimmune reaction against type II collagen in MRL/Mp-lpr/lpr (MRL/l) mouse in an experimental model of rheumatoid arthritis (RA). Anti-type II collagen antibodies were detectable in 3-week-old mice and preceded the appearance of rheumatoid factors. Furthermore, mesenchymal cells and tartrate-resistant acid phosphatase-positive cells began to accumulate remarkably in the periphysis, a fibrochondro-osseous area in the bone marrow vicinity. The numbers of these cells increased with mice age, together with serum levels of anti-type II collagen antibodies. Immunostaining of the periphysis revealed expression of type II collagen, IgG, C3, Mac-3, MHC class II antigen Ia, and cathepsin-L. Osteoclast-like cells and macrophage infiltration into the lesion area were confirmed by transmission electron microscopy. The results indicate that cartilage degeneration in MRL/l mouse may originate in the periphysis and progress via a pathway independent of synovial invasion.
机译:为了阐明类风湿关节炎(RA)实验模型中MRL / Mp-lpr / lpr / lpr(MRL / 1)小鼠中针对II型胶原的自身免疫反应的重要性,采用了免疫组织化学方法检查了软骨退变的早期阶段。在3周龄的小鼠中可检测到抗II型胶原蛋白抗体,并且出现在类风湿因子之前。此外,间充质细胞和抗酒石酸的酸性磷酸酶阳性细胞开始明显聚集在骨膜附近,即骨质疏松症。这些细胞的数量随着小鼠年龄的增长以及抗II型胶原蛋白抗体的血清水平的增加而增加。骨膜的免疫染色显示II型胶原蛋白,IgG,C3,Mac-3,MHC II类抗原Ia和组织蛋白酶-L的表达。透射电镜证实破骨细胞样细胞和巨噬细胞浸润进入病变区域。结果表明MRL / l小鼠的软骨变性可能起源于骨膜,并通过独立于滑膜浸润的途径进展。

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