首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Periarticular Bone Loss in Arthritis Is Induced by Autoantibodies Against Citrullinated Vimentin
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Periarticular Bone Loss in Arthritis Is Induced by Autoantibodies Against Citrullinated Vimentin

机译:关节炎在关节炎中的骨骨质损失是由对瓜氨酸的自身抗体引起的

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Periarticular bone loss is a long known but yet insufficiently understood phenomenon in patients with rheumatoid arthritis. This study investigated whether autoimmunity against citrullinated proteins is causally involved in triggering periarticular bone loss. Periarticular bone loss was studied in the standard antigen-induced arthritis (AIA) mouse model with methylated bovine serum albumin (mBSA) as well as a modified model with mutated citrullinated vimentin (MCV) alone or in combination with mBSA. Periarticular bone loss, subchondral osteoclastogenesis, as well as local expression of cytokines, osteoclast genes, and peptidylarginine deiminase (PAD) enzymes were assessed after arthritis induction. Immune cell and osteoclast precursor infiltration were detected in the periarticular bone marrow and local lymph nodes. In addition, periarticular bone loss was assessed upon challenge of mice with purified anti-MCV antibody. Despite inducing a milder form of arthritis than mBSA, MCV triggered significant periarticular bone loss associated with an increased infiltration of osteoclast precursors and mature osteoclasts in the periarticular bone marrow. MCV enhanced the expression of the osteoclast inducers RANKL and M-CSF, the cytokines IL-8, IL-1, IL-6, and TNF-alpha, as well as PAD2 and PAD4 enzymes in the periarticular bone marrow. Furthermore, also anti-MCV antibody challenge induced significant periarticular bone loss and local osteoclastogenesis in the mice. Autoimmunity against citrullinated vimentin triggers periarticular bone loss by osteoclast activation in the bone marrow. These findings may explain why periarticular bone loss is already found very early in the disease course of patients with rheumatoid arthritis. (C) 2017 American Society for Bone and Mineral Research.
机译:膜骨损失是一种漫长的知名度,但在类风湿性关节炎患者中理解现象。本研究研究了对瓜氨酸蛋白的自身免疫是否有因果涉及触发围绕膜骨质损失。在标准抗原诱导的关节炎(AIA)小鼠模型中研究了脑膜骨质损失,其甲基化牛血清白蛋白(MBSA)以及单独或与MBSA组合或与MBSA组合的改性模型。在关节炎诱导后评估了关节炎诱导后,在关节炎诱导后评估围绕骨质骨质损失,Subchondral骨骨质细胞发生,以及细胞因子,破骨细胞基因和肽基胺酰胺酶(垫)酶的局部表达。在面膜骨髓和局部淋巴结中检测免疫细胞和骨壳前体渗透。此外,对纯化的抗MCV抗体的小鼠的挑战评估了膜骨损失。尽管诱导了较高的关节炎形式而不是MBSA,但MCV引发了与骨髓骨髓内骨髓前体和成熟骨质体的浸润增加相关的显着围绕膜骨质损失。 MCV增强了破骨细胞诱导剂RANKL和M-CSF,细胞因子IL-8,IL-1,IL-6和TNF-α的表达,以及在膜骨髓中的PAD2和PAD4酶。此外,还抗MCV抗体攻击诱导小鼠中的显着膜骨损失和局部骨质细胞发生。骨髓内骨髓骨髓活化的自身免疫触发骨髓骨质损失。这些发现可以解释为什么在类风湿性关节炎患者的疾病过程中已经很早就发现了面膜骨质损失。 (c)2017年美国骨骼和矿物学学会。

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