Display Abstract

Title The role of CD200-CD200R in cancer immunoediting

Name Kang-Ling Liao
Country USA
Email liao.92@mbi.osu.edu
Co-Author(s) Kang-Ling Liao, Xue-Feng Bai, Avner Friedman
Submit Time 2014-03-31 10:14:52
Session
Special Session 62: Mathematical models of cell migration, tumor growth and cancer dynamics
Contents
CD200 is a cell membrane protein that interacts with CD200 receptor (CD200R) of myeloid lineage cells. During tumor initiation and progression, CD200-positive tumor cells can interact with M1 and M2 macrophages through CD200-CD200R-compex to silence macrophages. However, the functions of M1 and M2 cells in tumor growth are different, so CD200-CD200R has been shown to have apparently two contradictory experimental results in tumor growth: inhibition and promotion. We used a system approach to determine the combined effect of CD200-CD200R interaction on tumor proliferation by developing a mathematical model. We explained why these two opposite experimental results can both take place depending on the "affinity" of M1 and M2 macrophages to form the complex CD200-CD200R with tumor. If M1 cell has more affinity than M2 cell, then CD200-CD200R promotes tumor growth and block CD200-CD200R could be a good therapy. However, if M2 cell has more affinity than M1 cell, then we have opposite result that block CD200-CD200R will only increase tumor growth. Our results help understanding the complexities of tumor microenvironment.