19:10 - 21:00
Room: Ishikawa Ongakudō Interchange Hall
Poster Session
Induction of live cell phagocytosis by a specific combination of inflammatory stimuli
Takamasa Ishidome1, 2, Rikinari Hanayama1, 2
1Department of Immunologty, Kanazawa University Graduate School of Medicine, Takaramachi, Japan, 2Laboratory of Immune Network, Immunology Frontier Research Center (IFReC), Osaka University, Yamadaoka, Japan

Conditions of severe hyper-inflammation can lead to uncontrolled activation of macrophages, and the ensuing phagocytosis of live cells. However, relationships between inflammatory stimuli and uncontrolled phagocytosis of live cells by macrophages are poorly understood. To identify mediators of this process, we established in vitro phagocytosis assays of live cells by stimulating macrophages with CpG DNA, interferon-γ, and anti-interleukin-10 receptor antibody. In this model, various cell surface receptors were upregulated on macrophages, and phagocytosis of live cells was induced in a Rac1-dependent manner. Subsequent inhibition of the ICAM-1, VCAM-1, and both of these receptors specifically abolished in vitro and in vivo phagocytosis of live T cells, myeloid cells, and B cells, respectively. In addition, overexpression of ICAM-1 or VCAM-1 in non-phagocytic NIH3T3 cells led to active phagocytosis of live cells. These data indicate molecular mechanisms underlying live cell phagocytosis induced by hyper-inflammation, and this experimental model will be useful to clarify the pathophysiological mechanisms of hemophagocytosis and indicate therapeutic targets.


Reference:
Mo-P13-3
Session:
Poster Session 13 “Development and function of Macrophage and DC”
Presenter/s:
Takamasa Ishidome
Presentation type:
Poster Presentation
Room:
Ishikawa Ongakudō Interchange Hall
Date:
Monday, 30 October 2017
Time:
19:10 - 21:00
Session times:
19:10 - 21:00