Non-prenylatable, cytosolic Rac1 alters neurite outgrowth while retaining the ability to be activated
Autor: | Jordan A. McConnell, Jairus M. Reddy, Brian W. Beck, Cristina P. Reddy, DiAnna L. Hynds, Filsy Samuel |
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Rok vydání: | 2015 |
Předmět: |
rac1 GTP-Binding Protein
Cytoplasm GTP' Neurite Down-Regulation RAC1 GTPase Guanosine triphosphate Biology Cell morphology chemistry.chemical_compound Cell Line Tumor Cell Adhesion Neurites Animals Humans Lovastatin Mitogen-Activated Protein Kinase 1 Mitogen-Activated Protein Kinase 3 Cell Membrane Cell migration Cell Biology Rats Cell biology Amino Acid Substitution chemistry Signal transduction |
Zdroj: | Cellular Signalling. 27:630-637 |
ISSN: | 0898-6568 |
Popis: | Rac1 is an important regulator of axon extension, cell migration and actin reorganization. Like all Rho guanine triphosphatases (GTPases), Rac1 is targeted to the membrane by the addition of a geranylgeranyl moiety, an action thought to result in Rac1 guanosine triphosphate (GTP) binding. However, the role that Rac1 localization plays in its activation (GTP loading) and subsequent activation of effectors is not completely clear. To address this, we developed a non-prenylatable emerald green fluorescent protein (EmGFP)-Rac1 fusion protein (EmGFP-Rac1(C189A)) and assessed how expressing this construct affected neurite outgrowth, Rac1 localization and activation in neuroblastoma cells. Expression of EmGFP-Rac1(C189A) increased localization to the cytosol and induced cell clustering while increasing neurite initiation. EmGFP-Rac1(C189A) expression also increased Rac1 activation in the cytosol, compared to cells expressing wild-type Rac1 (EmGFP-Rac1). These results suggest that activation of Rac1 may not require plasma membrane localization, potentially leading to differential activation of cytosolic signaling pathways that alter cell morphology. Understanding the consequences of differential localization and activation of Rho GTPases, including Rac1, could lead to new therapeutic targets for treating neurological disorders. |
Databáze: | OpenAIRE |
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