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ABSTRACT: We examined the ability of sphingosine-1-phosphate (S1P) to desensitize extracellular signal-related kinase (ERK), a mitogen-activated protein kinase linked to antiapoptotic responses in the heart. In isolated adult mouse cardiomyocytes, S1P (10 nM-5 microM) induced ERK phosphorylation in a time- and dose-dependent manner. S1P stimulation of ERK was completely inhibited by an S1P1/3 subtype receptor antagonist (VPC23019), by a Gi protein inhibitor (pertussis toxin) and by a mitogen-activated protein kinase/ERK kinase inhibitor (PD98059). A selective S1P3 receptor antagonist (CAY10444) had no effect on S1P-induced ERK activation. The selective S1P1 agonist SEW2871 also induced ERK phosphorylation. Activation of ERK by restimulation with 100 nM S1P was suppressed after 1 hour of preincubation with 100 nM S1P but recovered fully the next day, suggesting receptor recycling. Similar results were obtained in protein kinase C epsilon-null cardiomyocytes. Treatment with the nonselective S1P receptor agonist FTY720 for 1 hour also reduced phospho-ERK expression in response to subsequent S1P stimulation. In contrast to S1P, some desensitization to FTY720 persisted after overnight exposure. Cell death induced by hypoxia/reoxygenation was reduced by pretreatment with exogenous S1P. This enhanced survival was abrogated by pretreatment with PD98059, VPC23019, or pertussis toxin. Thus, exogenous S1P induces rapid and reversible S1P1-mediated ERK phosphorylation. S1P-induced adult mouse cardiomyocyte survival requires ERK activation mediated via an S1P1-Gi pathway.
Journal of cardiovascular pharmacology 05/2009; 53(6):486-94. · 2.83 Impact Factor
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ABSTRACT: This study shows that the small GTP-binding protein ADP-ribosylation factor 6 (ARF6) is an important regulator of tumor growth and metastasis. Using spontaneous melanoma tumor growth assays and experimental metastasis assays in nude mice, we show that sustained activation of ARF6 reduces tumor mass growth but significantly enhances the invasive capacity of tumor cells. In contrast, mice injected with tumor cells expressing a dominantly inhibitory ARF6 mutant exhibited a lower incidence and degree of invasion and lung metastasis compared with control animals. Effects on tumor growth correlate with reduced cell proliferation capacity and are linked at least in part to alterations in mitotic progression induced by defective ARF6 cycling. Furthermore, phospho-ERK levels in subcultured cells from ARF6(GTP) and ARF6(GDP) tumor explants correlate with invasive capacity. ARF6-induced extracellular signal-regulated kinase (ERK) signaling leads to Rac1 activation to promote invadopodia formation and cell invasion. These findings document an intricate role for ARF6 and the regulation of ERK activation in orchestrating mechanisms underlying melanoma growth, invasion, and metastases.
Cancer Research 04/2009; 69(6):2201-9. · 7.86 Impact Factor
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ABSTRACT: Tumor cell invasion is a coordinated process involving the formation of invadopodia and the localized degradation of the extracellular matrix (ECM). The process of cell invasion is regulated by cell-signaling proteins such as Ras-related GTPases and members of the mitogen-activated protein kinase (MAPK) family. Our studies have focused on the role of the ADP-ribosylation factor 6 (ARF6) GTPase in the process of tumor cell invasion. Using activated and dominant negative mutants of ARF6 in a tumor cell culture model, our laboratory has demonstrated that the GTPase cycle of ARF6 regulates invadopodia formation and matrix degradation. Furthermore, ARF6-mediated cell invasion was found to be dependent on the activation of the extracellular signal-regulated kinase (ERK). These findings demonstrate a critical role for ARF6 in ERK activation and tumor cell invasion. To investigate the role of ARF6 in tumor cell invasion and ERK activation, a number of methods were employed. These procedures include transfection of LOX cells, in vitro matrix-degradation assays, immunofluorescence microscopy, and biochemical assays. These approaches can be applied effectively to measure the degree of invasiveness fostered by ARF6 and/or other GTPases and to examine the subcellular distribution of the molecular players that are trafficked or recruited to sites of cell invasion.
Methods in Enzymology 02/2005; 404:134-47. · 2.04 Impact Factor
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ABSTRACT: ATF6 is a 670-amino acid endoplasmic reticulum (ER) transmembrane protein that is cleaved in response to ER stress. The resulting N-terminal fragment of approximately 400 amino acids translocates to the nucleus and activates selected ER stress-inducible genes, such as GRP-78 and sarco/endoplasmic reticulum ATPase, which are required for cell survival. In studying the mechanism of ATF6-activated transcription, we found that when HeLa cells were transfected with a plasmid encoding ATF6-(1-373), ER stress-inducible reporter gene activation was high, but ATF6-(1-373) expression was low, unless a proteasome inhibitor was added. In contrast, transfection with a plasmid encoding ATF6-(94-373) resulted in low reporter activation and high expression of ATF6-(94-373), which was independent of the proteasome inhibitor. Thus, the information responsible for transcriptional activation and proteasomal degradation must lie within the N-terminal 93 amino acids of ATF6. This portion of ATF6 was found to be homologous to the herpes simplex viral protein, VP16. One 8-amino acid domain of particular interest in this region of ATF6 is 75% identical to the VN8 region in VP16. VN8 is required for VP16-mediated transcription, as well as rapid degradation of VP16 by proteasomes. Point mutations in the VN8-like region of ATF6 caused a loss of transcription, increased expression levels, and an increase in half-life. Thus, the potent transcriptional activities and rapid degradation of ATF6 and VP16 require the VN8 domains in each protein. Homology searches indicate that ATF6 is the only eukaryotic protein known that possesses an active VN8 domain, raising questions about how this domain evolved and the functional importance underlying its appearance in only these two transcription factors.
Journal of Biological Chemistry 07/2002; 277(23):20734-9. · 4.77 Impact Factor
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ABSTRACT: The recently described transcription factor, ATF6, mediates the expression of proteins that compensate for potentially stressful
changes in the endoplasmic reticulum (ER), such as reduced ER calcium. In cardiac myocytes the maintenance of optimal calcium
levels in the sarcoplasmic reticulum (SR), a specialized form of the ER, is required for proper contractility. The present
study investigated the hypothesis that ATF6 serves as a regulator of the expression of sarco/endoplasmic reticulum calcium
ATPase-2 (SERCA2), a protein that transports calcium into the SR from the cytoplasm. Depletion of SR calcium in cultured cardiac
myocytes fostered the translocation of ATF6 from the ER to the nucleus, activated the promoter for rat SERCA2, and led to
increased levels of SERCA2 protein. SERCA2 promoter induction by calcium depletion was partially blocked by dominant-negative
ATF6, whereas constitutively activated ATF6 led to SERCA2 promoter activation. Mutation analyses identified a promoter-proximal
ER stress-response element in the rat SERCA2 gene that was required for maximal induction by ATF6 and calcium depletion. Although
this element was shown to be responsible for all of the effects of ATF6 on SERCA2 promoter activation, it was responsible
for only a portion of the effects of calcium depletion. Thus, SERCA2 induction in response to calcium depletion appears to
be a potentially physiologically important compensatory response to this stress that involves intracellular signaling pathways
that are both dependent and independent of ATF6.
Journal of Biological Chemistry 12/2001; 276(51):48309-48317. · 4.77 Impact Factor
