Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/181262
Title: Cooperation of adenosine with macrophage Toll-4 receptor agonists leads to increased glycolytic flux through the enhanced expression of PFKFB3 gene
Author: Ruiz-García, Almudena
Monsalve, Eva
Novellasdemunt, Laura
Navarro i Sabaté, Àurea
Manzano Cuesta, Anna
Rivero, Samuel
Castrillo, Antonio
Casado, Marta
Laborda, Jorge
Bartrons Bach, Ramon
Díaz-Guerra, María José M.
Keywords: Adenosina
Macròfags
Expressió gènica
Adenosine
Macrophages
Gene expression
Issue Date: 3-Jun-2011
Publisher: American Society for Biochemistry and Molecular Biology
Abstract: Macrophages activated through Toll receptor triggering increase the expression of the A(2A) and A(2B) adenosine receptors. In this study, we show that adenosine receptor activation enhances LPS-induced pfkfb3 expression, resulting in an increase of the key glycolytic allosteric regulator fructose 2,6-bisphosphate and the glycolytic flux. Using shRNA and differential expression of A(2A) and A(2B) receptors, we demonstrate that the A(2A) receptor mediates, in part, the induction of pfkfb3 by LPS, whereas the A(2B) receptor, with lower adenosine affinity, cooperates when high adenosine levels are present. pfkfb3 promoter sequence deletion analysis, site-directed mutagenesis, and inhibition by shRNAs demonstrated that HIF1α is a key transcription factor driving pfkfb3 expression following macrophage activation by LPS, whereas synergic induction of pfkfb3 expression observed with the A(2) receptor agonists seems to depend on Sp1 activity. Furthermore, levels of phospho-AMP kinase also increase, arguing for increased PFKFB3 activity by phosphorylation in long term LPS-activated macrophages. Taken together, our results show that, in macrophages, endogenously generated adenosine cooperates with bacterial components to increase PFKFB3 isozyme activity, resulting in greater fructose 2,6-bisphosphate accumulation. This process enhances the glycolytic flux and favors ATP generation helping to develop and maintain the long term defensive and reparative functions of the macrophages.
Note: Reproducció del document publicat a: https://doi.org/10.1074/jbc.M110.190298
It is part of: Journal of Biological Chemistry, 2011, vol. 286, num. 22, p. 19247-19258
URI: http://hdl.handle.net/2445/181262
Related resource: https://doi.org/10.1074/jbc.M110.190298
ISSN: 0021-9258
Appears in Collections:Articles publicats en revistes (Infermeria Fonamental i Medicoquirúrgica)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Ciències Fisiològiques)

Files in This Item:
File Description SizeFormat 
595651.pdf2 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.