Rhipicephalus microplus salivary gland molecules induce differential CD86 expression in murine macrophages

Background: tick parasitism is a major impediment for cattle production in many parts of the world. the southern cattle tick,rhipicephalus (boophilus) microplus,is an obligate hematophagous parasite of domestic and wild animals that serves as vector of infectious agents lethal to cattle. tick saliva contains molecules evolved to modulate host innate and adaptive immune responses which facilitates blood feeding and pathogen transmission. tick feeding promotes cd4 t cell polarization to a th2 profile usually accompanied by down-regulation of th1 cytokines through as yet undefined mechanisms. co-stimulatory molecules on antigen presenting cells are central to development of t cell responses including th1 and th2 responses. tick induced changes to antigen presenting cell signal transduction pathways are largely unknown. here we document the ability of r. microplus salivary gland extracts (sge) to effect differential cd86 expression. results. we examined changes in co-stimulatory molecule expression in murine raw 264.7 cells in response to r. microplus sge exposure in the presence of the toll-like receptor 4 (tlr4) ligand,lps. after 24 hrs,cd86,but not cd80,was preferentially up-regulated on mouse macrophage raw 264.7 cells when treated with sge and then lps,but not sge alone. cd80 and cd40 expression was increased with lps,but the addition of sge did not alter expression. higher concentrations of sge were less effective at increasing cd86 rna expression. the addition of mitogen or extracellular kinase (mek) inhibitor,pd98059,significantly reduced the ability for sge to induce cd86 expression,indicating activation of mek is necessary for sge induced up-regulation. conclusions. molecules in sge of r. microplus have a concentration-dependent effect on differential up-regulation of cd86 in a macrophage cell line activated by the tlr4 ligand,lps. this cd86 up-regulation is at least partially dependent on the erk1/2 pathway and may serve to promote th2 polarization of the immune response. © 2010 brake et al; licensee biomed central ltd.