Interestingly, VLRB-transfected human cell lines, such as HEK293T cells, produce oligomeric VLRB antibodies. Therefore, cell lines transfected with a VLRB-enriched cDNA library derived from immunized lamprey LLCs can establish antigen-specific

VLRB monoclonal antibodies. These VLRB antibodies retain antigen binding ability even after storage for > 12 months at 4°C, 1 month at room temperature, or 36 hrs at 56°C. Additionally, although these VLRB antibodies cannot be eluted from an antigen-affinity column with high salt concentrations or under extremely acidic conditions (pH < 1.5), they can be eluted under highly basic conditions (pH > 11). This suggests that VLRB antibodies may be useful natural single-chain alternatives to immunoglobulin-based antibodies for biotechnology applications. Crystallographic analysis of VLRA and VLRB has shown that they adopt a horseshoe-shaped structure in lampreys and hagfish (Fig. 3)

[29], [30]. The crystal structure of VLRC is not INCB018424 molecular weight yet available; however, three-dimensional modeling predicts selleck chemicals llc that the overall structure of VLRC is similar to that of VLRA and VLRB. Parallel beta sheets that contain most of the variable residues form the concave surface. Recently, crystallographic analyses of VLRA and VLRB binding to HEL were reported [31], [32]. In these VLR-HEL complexes, HEL binds with VLRA and VLRB molecules via both LRR modules and protrusions in the LRRCT domain. A stretch of amino acid residues known as the HVI, which is highly variable in length, amino acid composition and secondary structure, forms these protrusions (Fig. 3) [29]. Unlike VLRA and VLRB, VLRC lacks HVI in the LRRCT domain. This why structural feature might impose additional restrictions on the nature of antigens recognized by VLRC. VLR genes are assembled in distinct populations of LLCs. VLRB+ LLCs respond to antigens by undergoing lymphoblastoid transformation, proliferating and differentiating into plasmacytes that secrete multimeric antigen-specific VLRB antibodies [23]. In contrast, VLRA+ LLCs respond to T cell mitogens by upregulating their expression of IL-17 in a manner that is similar to

that of T helper 17 cells in jawed vertebrates, but not by secreting VLRA molecules [27]. The gene expression profiles of VLRA+ and VLRB+ LLCs are similar to those of mammalian T and B cells, respectively. For example, VLRA+ LLCs express genes associated with T cell differentiation and development (e.g., GATA binding protein 2/3, c-Rel, aryl hydrocarbon receptor, B cell leukemia/lymphoma 11B and CD45). VLRB+ LLCs express both spleen tyrosine kinase and B cell adaptor protein, which function in BCR-mediated signal transduction. In mammals, helper CD4+ T cells are required for antibody production from activated B cells. Interestingly, VLRA+ LLCs express IL-17 and the receptor for IL-8, whereas VLRB+ LLCs express IL-8 and the receptor for IL-17. These cytokines and their receptors may play a role in crosstalk between VLRA+ and VLRB+ LLCs.