Blockade of macrophage adhesion to CD200‐treated polystyrene culture surface

Abstract CD200 is an anti‐inflammatory transmembrane glycoprotein in the immunoglobulin superfamily. The interaction of CD200 and its receptor CD200R has shown to inhibit inflammatory response of myeloid cells to foreign materials. The purpose of this study is to create a CD200 immobilized biomaterial surface through polydopamine coating to suppress macrophage cell adhesion and reduce inflammatory cytokine secretion accordingly by macrophages. In this study, tissue‐culture treated polystyrene (TCPS) surface was modified with biotin through polydopamine coating. Purified CD200‐streptavidin fusion protein was then immobilized onto the biotinylated TCPS surface through the high affinity between biotin and streptavidin. Mouse J774A.1 macrophages were seeded on CD200‐immobilized TCPS surface to evaluate the effect of CD200 on preventing macrophage attachment. The effects of CD200‐immobilized TCPS surface on pro‐inflammatory cytokine secretion from J774A.1 macrophages were measured by enzyme‐linked immunosorbent assay. As a result, CD200‐immobilized TCPS surface suppressed macrophage attachment for up to 9 hr. The level of IL‐6 and TNF‐α secreted from J774A.1 macrophages interacted with CD200‐coated TCPS surface was reduced by 36.3% and 32.4%, respectively.