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纤溶酶原缺乏在不同类风湿性关节炎模型中的不同作用

Contrasting roles of plasminogen deficiency in different rheumatoid arthritis models.

作者信息

Li Jinan, Guo Yongzhi, Holmdahl Rikard, Ny Tor

机构信息

Umeå University, Sweden.

出版信息

Arthritis Rheum. 2005 Aug;52(8):2541-8. doi: 10.1002/art.21229.

Abstract

OBJECTIVE

To investigate the contrasting roles of plasminogen deficiency between models of collagen-induced arthritis (CIA) and antigen-induced arthritis (AIA).

METHODS

We developed a new animal model of arthritis, which we have called local injection-induced arthritis (LIA). In this model, we replaced methylated bovine serum albumin, which is normally used as an immunogen and is injected intraarticularly into the knee joint, with type II collagen (CII) to induce AIA. The severity of CIA, LIA, and AIA in wild-type and plasminogen-deficient mice was evaluated by clinical scoring or histologic grading. Necrosis was determined by histology and immunohistochemistry.

RESULTS

After CII immunization alone, wild-type mice developed arthritis in most of the paws as well as in the knee joints, whereas plasminogen-deficient mice were totally resistant to the disease. Local knee injections of CII or saline slightly enhanced the severity of the knee arthritis in wild-type mice during a 60-day experimental period. Unexpectedly, the plasminogen-deficient mice also developed arthritis in joints that were injected with CII or saline. However, the arthritis was milder than that in their wild-type littermates. Sustained tissue necrosis was found only in the plasminogen-deficient mice after the local injection.

CONCLUSION

Our data show that both the antigen and the joint trauma caused by the local injection are critical to explaining the contrasting roles of plasminogen deficiency in CIA and AIA. This further indicates that CIA and AIA have distinct pathogenic mechanisms. The data also suggest that plasmin may be required for the induction of these arthritis models that are critically dependent on complement activation.

摘要

目的

研究纤溶酶原缺乏在胶原诱导性关节炎(CIA)模型和抗原诱导性关节炎(AIA)模型中的不同作用。

方法

我们开发了一种新的关节炎动物模型,称为局部注射诱导性关节炎(LIA)。在该模型中,我们用II型胶原(CII)替代通常用作免疫原并关节内注射到膝关节的甲基化牛血清白蛋白来诱导AIA。通过临床评分或组织学分级评估野生型和纤溶酶原缺陷小鼠中CIA、LIA和AIA的严重程度。通过组织学和免疫组织化学确定坏死情况。

结果

仅用CII免疫后,野生型小鼠的大多数爪子以及膝关节都出现了关节炎,而纤溶酶原缺陷小鼠对该疾病完全有抵抗力。在60天的实验期内,局部膝关节注射CII或生理盐水会轻微加重野生型小鼠膝关节关节炎的严重程度。出乎意料的是,纤溶酶原缺陷小鼠在注射CII或生理盐水的关节也出现了关节炎。然而,其关节炎比野生型同窝小鼠的要轻。局部注射后仅在纤溶酶原缺陷小鼠中发现持续的组织坏死。

结论

我们的数据表明,抗原和局部注射引起的关节创伤对于解释纤溶酶原缺乏在CIA和AIA中的不同作用至关重要。这进一步表明CIA和AIA具有不同的致病机制。数据还表明,对于这些严重依赖补体激活的关节炎模型的诱导,纤溶酶可能是必需的。

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