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Regulator of G Protein Signaling 1 Suppresses CXCL12-Mediated Migration and AKT Activation in RPMI 8226 Human Plasmacytoma Cells and Plasmablasts
Authors:Hyo-Kyung Pak  Minchan Gil  Yoonkyung Lee  Hyunji Lee  A-Neum Lee  Jin Roh  Chan-Sik Park
Institution:1. Cell Dysfunction Research Center, University of Ulsan College of Medicine, Seoul, Korea.; 2. Institute for Life Sciences, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.; 3. Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.; Imperial College London, UNITED KINGDOM,
Abstract:Migration of plasma cells to the bone marrow is critical factor to humoral immunity and controlled by chemokines. Regulator of G protein signaling 1 (RGS1) is a GTPase-activating protein that controls various crucial functions such as migration. Here, we show that RGS1 controls the chemotactic migration of RPMI 8226 human plasmacytoma cells and human plasmablasts. LPS strongly increased RGS1 expression and retarded the migration of RPMI 8226 cells by suppressing CXCL12-mediated AKT activation. RGS1 knockdown by siRNA abolished the retardation of migration and AKT suppression by LPS. RGS1-dependent regulation of migration via AKT is also observed in cultured plasmablasts. We propose novel functions of RGS1 that suppress AKT activation and the migration of RPMI 8226 cells and plasmablasts in CXCL12-mediated chemotaxis.
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