Imaging and measuring the biophysical properties of Fc gamma receptors on single macrophages using atomic force microscopy

• Published in: Biochemical and biophysical research communications 2013-09, Vol.438 (4), p.709-714
• Main Authors: Li, Mi, Liu, Lianqing, Xi, Ning, Wang, Yuechao, Xiao, Xiubin, Zhang, Weijing
• Format: Article
• Language: English
• Subjects: 60 APPLIED LIFE SCIENCES; AFFINITY; Animals; ANTIBODIES; Antibodies, Monoclonal - immunology; Antibody; ATOMIC FORCE MICROSCOPY; Cell Line; Fc gamma receptor; FINE STRUCTURE; IMMUNOTHERAPY; Macrophage; MACROPHAGES; Macrophages - cytology; Macrophages - immunology; Macrophages - ultrastructure; Mice; Microscopy, Atomic Force - methods; NANOSTRUCTURES; NATURAL KILLER CELLS; NEOPLASMS; POLYETHYLENE GLYCOLS; RECEPTORS; Receptors, IgG - analysis; Receptors, IgG - immunology
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2013.07.114

•Nanoscale cellular ultra-structures of macrophages were observed.•The binding affinities of FcγRs were measured directly on macrophages.•The nanoscale distributions of FcγRs were mapped on macrophages. Fc gamma receptors (FcγR), widely expressed on effector cells (e.g., NK cells, macrophages), play an important role in clinical cancer immunotherapy. The binding of FcγRs to the Fc portions of antibodies that are attached to the target cells can activate the antibody-dependent cell-mediated cytotoxicity (ADCC) killing mechanism which leads to the lysis of target cells. In this work, we used atomic force microscopy (AFM) to observe the cellular ultra-structures and measure the biophysical properties (affinity and distribution) of FcγRs on single macrophages in aqueous environments. AFM imaging was used to obtain the topographies of macrophages, revealing the nanoscale cellular fine structures. For molecular interaction recognition, antibody molecules were attached onto AFM tips via a heterobifunctional polyethylene glycol (PEG) crosslinker. With AFM single-molecule force spectroscopy, the binding affinities of FcγRs were quantitatively measured on single macrophages. Adhesion force mapping method was used to localize the FcγRs, revealing the nanoscale distribution of FcγRs on local areas of macrophages. The experimental results can improve our understanding of FcγRs on macrophages; the established approach will facilitate further research on physiological activities involved in antibody-based immunotherapy.