Delayed apoptotic cell clearance and lupus-like autoimmunity in mice lacking the c-mer membrane tyrosine kinase

被引:509
作者
Cohen, PL
Caricchio, R
Abraham, V
Camenisch, TD
Jennette, JC
Roubey, RAS
Earp, HS
Matsushima, G
Reap, EA
机构
[1] Univ Penn, Dept Med, Div Rheumatol, Philadelphia, PA 19104 USA
[2] Philadelphia Vet Affairs Med Ctr, Philadelphia, PA 19104 USA
[3] Mayo Clin, Dept Biochem & Mol Biol, Scottsdale, AZ 85259 USA
[4] Univ N Carolina, Dept Pathol, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Dept Med, Chapel Hill, NC 27599 USA
[6] Univ N Carolina, Dept Microbiol Immunol, Chapel Hill, NC 27599 USA
[7] AlphaVax, Durham, NC 27709 USA
关键词
autoimmunity; Lupus Erythematosus; systemic; phagocytosis; apoptosis; macrophages;
D O I
10.1084/jem.20012094
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mice lacking the membrane tyrosine kinase c-mer have been shown to have altered macrophage cytokine production and defective phagocytosis of apoptotic cells despite normal phagocytosis of other particles. We show here that c-mer-deficient mice have impaired clearance of infused apoptotic cells and that they develop progressive lupus-like autoimmunity, with antibodies to chromatin, DNA, and IgG. The autoimmunity appears to be driven by endogenous antigens, with little polyclonal B cell activation. These mice should be an excellent model for studying the role of apoptotic debris as an immunogenic stimulus for systemic autoimmunity.
引用
收藏
页码:135 / 140
页数:6
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