UM
Activation of the small GTPase Rac1 by cGMP-dependent protein kinase
Hou Y.1; Ye R.D.2; Browning D.D.1
2004
Source PublicationCellular Signalling
ISSN08986568
Volume16Issue:9Pages:1061-1069
AbstractCyclic-GMP-dependent protein kinase (PKG) is widely appreciated as having diverse roles in a variety of cell types. Many reports have indicated that PKG might regulate cell function by activating members of the mitogen-activated protein kinase (MAPK) family of signaling proteins. In this study, stimulation of HEK-293 cells with nitric oxide (NO) was found to induce a rapid accumulation of phosphorylated p38 MAPK. The involvement of PKG in this process was confirmed by cotransfection of a dominant negative PKG construct (G1αR-GFP), which was able to block cGMP-induced p38 MAPK activation. Transfection of cells to express dominant negative Rac1(T17N) was also able to dose-dependently block cGMP-stimulated activation of p38 MAPK, thus indicating the importance of this pathway downstream of PKG. GST-PDB affinity-precipitation experiments revealed that stimulation of HEK293 cells with either nitric oxide or 8-Br-cGMP resulted in a rapid and transient activation of Rac1 with similar kinetics to p38 MAPK phosphorylation. Moreover, using in vitro kinase assays it was found that cGMP also stimulated the activity of the Rac1 effector Pak1. The activation of both Rac1 and Pak1 by 8-Br-cGMP was completely abolished by transfection of the cells with G1αR-GFP. Expression of the Rac1(T17N) mutant inhibited PKG-dependent activation of PAK1 indicating that Rac1 functions upstream of PAK1 in this pathway. Immunofluorescence experiments demonstrated clear colocalization of PKG and Rac1 in membrane ruffles and dynamic membrane regions supporting a functional interaction. However, in vitro kinase assays demonstrated that Rac1 is not a substrate for PKG suggesting an indirect activation mechanism. Taken together these data demonstrate a novel PKG-dependent pathway by which the Rac1/Pak1 pathway is activated. Furthermore, we demonstrate that this pathway is central to the activation of p38 MAPK by PKG in these cells. © 2004 Elsevier Inc. All rights reserved.
Keyword8-Br-cGMP 8-bromo cyclic guanosine monophosphate cGMP-dependent protein kinase FBS fetal bovine serum GFP glutathione-S-transferase GST p21 activated protein kinase Pak Pak binding domain for Rac PBD PBS phosphate buffered saline PKG
DOI10.1016/S0898-6568(04)00033-6
URLView the original
Language英語
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Cited Times [WOS]:32   [WOS Record]     [Related Records in WOS]
Document TypeJournal article
CollectionUniversity of Macau
Affiliation1.Medical College of Georgia
2.University of Illinois at Chicago
Recommended Citation
GB/T 7714
Hou Y.,Ye R.D.,Browning D.D.. Activation of the small GTPase Rac1 by cGMP-dependent protein kinase[J]. Cellular Signalling,2004,16(9):1061-1069.
APA Hou Y.,Ye R.D.,&Browning D.D..(2004).Activation of the small GTPase Rac1 by cGMP-dependent protein kinase.Cellular Signalling,16(9),1061-1069.
MLA Hou Y.,et al."Activation of the small GTPase Rac1 by cGMP-dependent protein kinase".Cellular Signalling 16.9(2004):1061-1069.
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