Non-redundant and critical roles for leukotriene B4 receptors BLT1 and BLT2 in mouse models of inflammatory arthritis.

Leukotriene;Inflammatory arthritis;Arthritis

Steven Mathis, 1979-

University:University of Louisville

Department:Microbiology and Immunology

关键词: Leukotriene;    Inflammatory arthritis;    Arthritis;   

Others  :  https://ir.library.louisville.edu/cgi/viewcontent.cgi?article=1919&context=etd

美国|英语

来源: The Universite of Louisville's Institutional Repository

【 摘 要 】

Inflammation is now recognized as an important factor in several age-related diseases such as arthritis, atherosclerosis, multiple sclerosis and diabetes. In each case, sub-clinical chronic inflammation occurs over years and leads to progressive destruction of the tissue until the symptoms become clinically apparent. Eicosanoids such as prostaglandins and leukotrienes play an important role in inflammation. Among these, leukotriene B 4 (LTB 4 ) has had a long history of being associated with numerous inflammatory diseases. A high affinity receptor for LTB 4 , LTB 4 receptor 1 (BLT 1) has been well-characterized in human and murine tissues. While the molecular mechanisms remain unclear, its importance in diverse inflammatory diseases was demonstrated in mice lacking BLT1. More recently, a second highly conserved low affinity LTB 4 receptor, LTB 4 receptor 2 (BLT2) was identified, but its functional significance remains completely unknown. Both BLT1 and BLT2 are seven-transmembrane G protein coupled receptors transducing signals through heterotrimeric G-proteins. Chapter II of this thesis describes the generation and characterization of monoclonal antibodies to BLT1. Immunization of BLT1-deficient mice with 300.19, a murine pre-B cell line expressing high levels of either human or murine BLT1 allowed isolation of highly species specific anti-BLT1 antibodies. Using an approach involving a series of human/murine BLT1 chimeric receptors the monoclonal antibody binding sites were mapped to extracellular loop-2. Extensive characterization of BLT1 in murine primary cells revealed high levels of BLT1 in neutrophils and eosinophils and a previously unsuspected regulation of BLT1 in macrophages. While bone marrow derived macrophages expressed high levels of BLT1 its expression in peripheral tissue macrophages was significantly reduced suggesting a potential novel mechanism, and a role for BLT1 in inflammation-induced egress of bone marrow derived cells. The antibodies also allowed demonstration of normal BLT1 expression in the recently generated BLT2 deficient mice. Future studies could explore the therapeutic potential of these antibodies. In Chapter III, we investigated the role of BLT1 and BLT2 in inflammatory arthritis in mouse models. Collagen induced arthritis (CIA) is a model where mice are immunized with chicken collagen type II in complete freund's adjuvant and leads to a polyarthritis in the distal joints. BLT1 deficient mice on the DBA/1 background were completely protected from the development of CIA which confirms the previous observations with BLT1 antagonists and BLT1 deficient mice on the C57B1/6 background. Arthritis was also induced by transfer of K/BxN serum to naÏve mice. K/BxN is a