scholarly journals Ability of Monocyte-Derived Dendritic Cells To Secrete Oxygen Radicals in Response to Formyl Peptide Receptor Family Agonists Compared to That of Myeloid and Plasmacytoid Dendritic Cells

2007 ◽  
Vol 14 (3) ◽  
pp. 328-330 ◽  
Author(s):  
Anna Karlsson ◽  
Erik Nygren ◽  
Jennie Karlsson ◽  
Inger Nordström ◽  
Claes Dahlgren ◽  
...  

ABSTRACT We show that human monocyte-derived dendritic cells (DC) differ considerably from freshly isolated blood-derived myeloid and plasmacytoid DC in their abilities to produce reactive oxygen species in response to different agonists to the formyl peptide receptor family and are thus poor representatives of blood DC in this field of research.

2019 ◽  
Vol 2019 ◽  
pp. 1-17 ◽  
Author(s):  
Martina Castaldo ◽  
Cristiana Zollo ◽  
Gabriella Esposito ◽  
Rosario Ammendola ◽  
Fabio Cattaneo

Several enzymes are capable of producing reactive oxygen species (ROS), but only NADPH oxidases (NOX) generate ROS as their primary and sole function. In the central nervous system, NOX2 is the major source of ROS, which play important roles in signalling and functions. NOX2 activation requires p47phox phosphorylation and membrane translocation of cytosolic subunits. We demonstrate that SH-SY5Y cells express p47phox and that the stimulation of Formyl-Peptide Receptor 1 (FPR1) by N-fMLP induces p47phox phosphorylation and NOX-dependent superoxide generation. FPR1 is a member of the G protein-coupled receptor (GPCR) family and is able to transphosphorylate several tyrosine kinase receptors (RTKs). This mechanism requires ROS as signalling intermediates and is necessary to share information within the cell. We show that N-fMLP stimulation induces the phosphorylation of cytosolic Y490, Y751, and Y785 residues of the neurotrophin receptor TrkA. These phosphotyrosines provide docking sites for signalling molecules which, in turn, activate Ras/MAPK, PI3K/Akt, and PLC-γ1/PKC intracellular cascades. N-fMLP-induced ROS generation plays a critical role in FPR1-mediated TrkA transactivation. In fact, the blockade of NOX2 functions prevents Y490, Y751, and Y785 phosphorylation, as well as the triggering of downstream signalling cascades. Moreover, we observed that FPR1 stimulation by N-fMLP also improves proliferation, cellular migration, and neurite outgrowth of SH-SY5Y cells.


2008 ◽  
Vol 8 (6) ◽  
pp. 765-776 ◽  
Author(s):  
C JOHN ◽  
F GAVINS ◽  
N BUSS ◽  
P COVER ◽  
J BUCKINGHAM

2009 ◽  
Vol 183 (9) ◽  
pp. 5511-5517 ◽  
Author(s):  
Sang Doo Kim ◽  
Jung Mo Kim ◽  
Seong Ho Jo ◽  
Ha Young Lee ◽  
Sun Young Lee ◽  
...  

2017 ◽  
Vol 85 ◽  
pp. 64-77 ◽  
Author(s):  
Keqiang Chen ◽  
Zhiyao Bao ◽  
Wanghua Gong ◽  
Peng Tang ◽  
Teizo Yoshimura ◽  
...  

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