Mol. Cells 2012; 34(2): 159-164
Published online July 18, 2012
https://doi.org/10.1007/s10059-012-0055-9
© The Korean Society for Molecular and Cellular Biology
Correspondence to : *Correspondence: jrlee@ewha.ac.kr
We studied the role of a RhoA-specific guanine nucleo-tide exchange factor (p190RhoGEF) in dendritic cells (DCs), using transgenic (TG) mice that over-express a full gene of p190RhoGEF under the control of an invariant chain promoter. TG mice lacked localization of activated DCs to the T cell zone in the spleen and had reduced serum levels of IL-6 in response to lipopolysaccharide (LPS) injection. DCs from these mice also showed reduced surface expression of CD86, CD40, and CD205, but not MHCII, as well as a reduced capability to uptake antigen. Moreover, chemokine- driven migration and secretion of IL-6, but not of IL-12, were impaired after LPS-stimulation of TG DCs. Collectively, these results suggest that over-expressing p190RhoGEF nega-tively regulates conventional DC function in response to bacterial LPS infection.
Keywords dendritic cells, lipopolysaccharides, p190RhoGEF
Mol. Cells 2012; 34(2): 159-164
Published online August 31, 2012 https://doi.org/10.1007/s10059-012-0055-9
Copyright © The Korean Society for Molecular and Cellular Biology.
Hee Jung Seul1, Yu Ri Ahn1, Hyeon Myeong Song1, Yun Jung Ha1, and Jong Ran Lee1,2,3,*
1Division of Life and Pharmaceutical Sciences, Ewha Womans University, Seoul 120-750, Korea, 2Department of Life Science, College of Natural Sciences, Ewha Womans University, Seoul 120-750, Korea, 3Center for Cell Signaling and Drug Discovery Research, Ewha Womans University, Seoul 120-750, Korea
Correspondence to:*Correspondence: jrlee@ewha.ac.kr
We studied the role of a RhoA-specific guanine nucleo-tide exchange factor (p190RhoGEF) in dendritic cells (DCs), using transgenic (TG) mice that over-express a full gene of p190RhoGEF under the control of an invariant chain promoter. TG mice lacked localization of activated DCs to the T cell zone in the spleen and had reduced serum levels of IL-6 in response to lipopolysaccharide (LPS) injection. DCs from these mice also showed reduced surface expression of CD86, CD40, and CD205, but not MHCII, as well as a reduced capability to uptake antigen. Moreover, chemokine- driven migration and secretion of IL-6, but not of IL-12, were impaired after LPS-stimulation of TG DCs. Collectively, these results suggest that over-expressing p190RhoGEF nega-tively regulates conventional DC function in response to bacterial LPS infection.
Keywords: dendritic cells, lipopolysaccharides, p190RhoGEF
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