Role of C3a Receptors, C5a Receptors, and Complement Protein C6 Deficiency in Collagen Antibody-Induced Arthritis in Mice

被引:107
作者
Banda, Nirmal K. [2 ]
Hyatt, Stephanie [2 ]
Antonioli, Alexandra H. [2 ]
White, Jason T. [2 ]
Glogowska, Magdalena [2 ]
Takahashi, Kazue [3 ]
Merkel, Tod J. [4 ]
Stahl, Gregory L. [5 ]
Mueller-Ortiz, Stacey [6 ]
Wetsel, Rick [6 ]
Arend, William P. [2 ]
Holers, V. Michael [1 ,2 ]
机构
[1] Univ Colorado, Sch Med, Div Rheumatol, BDC,Dept Med, Aurora, CO 80045 USA
[2] Univ Colorado, Sch Med, Dept Immunol, Aurora, CO 80045 USA
[3] Massachusetts Gen Hosp Children, Boston, MA 02114 USA
[4] US FDA, Div Bacterial Prod, Lab Resp Pathogens, Ctr Biol Evaluat & Res, Rockville, MD 20852 USA
[5] Brigham & Womens Hosp, Ctr Expt Therapeut & Reperfus Injury, Boston, MA 02115 USA
[6] Univ Texas Houston, Inst Mol Med, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
MEMBRANE ATTACK COMPLEX; EFFECTOR PHASE; RHEUMATOID-ARTHRITIS; PASSIVE TRANSFER; ANAPHYLATOXIN RECEPTOR; JOINT DESTRUCTION; DENDRITIC CELLS; ACTIVATION; C5L2; EXPRESSION;
D O I
10.4049/jimmunol.1102310
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The complement system, especially the alternative pathway, plays essential roles in the induction of injury in collagen Ab-induced arthritis (CAIA) in mice. The goal of the current study was to directly compare the roles of receptors for C3a and C5a, as well as the membrane attack complex, as effector mechanisms in the pathogenesis of CAIA. Clinical disease activity in C3aR(-/-), C5aR(-/-), and C6-deficient (C6-def) mice was decreased by 52, 94, and 65%, respectively, as compared with wild-type mice. Decreases in histopathologic injury as well as in IgG and C3 deposition paralleled the clinical disease activity. A decrease in the percentage of synovial neutrophils was observed in C3aR(-/-), C5aR(-/-), and C6-def mice, and a decrease in macrophages was observed in C3aR(-/-) and C5aR(-/-), but not in C6-def, mice. Synovial mRNA obtained by laser capture microdissection exhibited a decrease in TNF-alpha in C5aR(-/-) mice and in IL-1 beta in both C5aR(-/-) and C6-def mice, whereas C3aR(-/-) mice demonstrated no change in either cytokine. Our findings show that absent C3aR-, C5aR-, or membrane attack complex-initiated effector mechanisms each decrease susceptibility to CAIA, with clinical effects most pronounced in C5aR-deficient mice. Although the absence of C3aR, C5aR, or C6 led to differential deficiencies in effector mechanisms, decreased proximal joint IgG and C3 deposition was common to all three genotypes in comparison with wild-type mice. These data suggest the existence of positive-feedback amplification pathways downstream of all three effectors that promote additional IgG deposition and C3 activation in the joint. The Journal of Immunology, 2012, 188: 1469-1478.
引用
收藏
页码:1469 / 1478
页数:10
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