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Vol. 19, Issue 6, 2609-2619, June 2008
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Kidney Disease Center, Department of Medicine, Division of Nephrology, Medical College of Wisconsin, Milwaukee, WI 53226
Submitted May 9, 2007;
Revised March 18, 2008;
Accepted March 25, 2008
Monitoring Editor: Carl-Henrik Heldin
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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; Daniels et al., 1999). GEF proteins contain a pleckstrin homology (PH) domain and the catalytic Dbl homology (DH) domain. In addition to these domains, β1Pix contains a Src homology 3 (SH3) domain that binds with high affinity to a polyproline stretch in Pak1 (p21-activated kinase; Manser et al., 1998). β1Pix also binds GIT1 through a GIT1-binding domain (Zhao et al., 2000). The leucine zipper (LZ) domain at the C-terminus mediates β1Pix homodimerization (Kim et al., 2001). There is mounting evidence showing that Pix functions as an integrator of signaling pathways controlling adhesion and cytoskeletal organization. Recently we have shown that endothelin-1 (ET-1) induces β1Pix translocation to focal adhesions through a PKA-dependent pathway (Chahdi et al., 2005). Pix was found to form a complex with paxillin, Pak, and p95PKL, which regulates cytoskeletal remodeling (Turner et al., 1999). Moreover, the Pak-Pix-GIT complex has been shown to target and regulate focal adhesions (Zhao et al., 2000). Recent study showed that the same complex plays a role in a different location where GIT1 functions as a scaffold protein to target Pix and Pak to the centrosome resulting in the activation of the centrosomal kinase Aurora-A (Zhao et al., 2005).
The adaptor protein Shc exists in three isoforms with relative molecular masses (Kd) of 46, 52, and 66 (Pelicci et al., 1992). They consist of a phosphotyrosine binding domain (PTB), a collagen homology domain (CH1) and a C-terminal Src homology 2 domain (SH2). In addition, p66Shc has a collagen homology domain 2 (CH2) at the N-terminus in which Ser36 is located. The serine 36 is phosphorylated in response to oxidative stress and appears to be critical for coupling Shc to stress response leading to apoptosis (Migliaccio et al., 1997). p66Shc knockout mice had a 30% increase in average lifespan when compared with control animals (Migliaccio et al., 1999). This increased longevity has been linked to enhanced resistance to oxidative stress. We have previously demonstrated the crucial role of p52Shc tyrosine phosphorylation in ET-1–mediated Ras activation in mesangial cells (Foschi et al., 1997). This phosphorylation enables and stabilizes the formation of a Shc-Grb2 complex and its subsequent association with Ras exchange factor Sos (Son of sevenless) facilitates the biphasic activation of Ras (Foschi et al., 1997). p46Shc has also been shown to bind Sos and Grb2 and mediate signals from receptor tyrosine kinase to the MAPK pathway (Pelicci et al., 1992; Egan et al., 1993). Although it can be tyrosine-phosphorylated (Bonfini et al., 1992; Migliaccio et al., 1997), serine 36 phosphorylation appears to be the main mechanism of p66Shc activation. Recent study established a link between p66Shc and FOXO3a where serine 36 phosphorylation has been shown to regulate FOXO3a phosphorylation (Nemoto and Finkel, 2002). In addition, oxidative stress no longer stimulated phosphorylation of FOXO3a in p66Shc deficient cells.
FOXO3a is a member of a large family of forkhead transcription factors that also contains FOXO1 and FOXO4. In the nematode Caenorhabditis elegans, the gene encoding DAF-16 (FOXO3a in mammals) promotes cell survival in response to nutrient starvation (Lin et al., 2001). Forkhead transcription factors are phosphorylated by Akt resulting in their export from the nucleus to the cytoplasm and, hence, a decrease in transcriptional activity of their target genes and enhanced cell survival and proliferation (Brunet et al., 1999; Kops et al., 1999). These forkhead factors inhibit cell cycle progression at the G1/S transition by controlling transcription of the cyclin-dependent kinase inhibitor p27kip1 (Brunet et al., 2001; Nakamura et al., 2000), although a p27kip1-independent mechanism may exist (Medema et al., 2000).
The elevated expression of both β1Pix and p66Shc in breast cancer cells (Jackson et al., 2000; Bae et al., 2005) suggests that both proteins may be involved in regulating cell proliferation, although p66Shc has been shown recently to inhibit T-cell proliferation (Pacini et al., 2004). In addition to its vasoactive property, ET-1 also controls cell proliferation and genes expression (Sugimoto et al., 2001). We found that ET-1 stimulation increases βPix and p66Shc expression. The relationship between βPix and p66Shc is not known. In this study we investigated the physical and functional coupling between βPix and p66Shc and the role of βPix in cell proliferation. Our data suggest the existence of novel signaling pathway initiated by ET-1–dependent formation of trimeric signaling complex βPix/p66Shc/FOXO3a, resulting in previously unknown Akt-independent mechanism of FOXO3a inactivation which promotes cell proliferation.
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MATERIALS AND METHODS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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) and primary HMCs were cultured in RPMI 1640 supplemented with 10% fetal bovine serum, penicillin (100 U/ml), and streptomycin (100 µg/ml) in a 37°C humidified incubator with 5% CO2. Transient transfection of HMCs with mammalian expression vectors were performed using Lipofectamine 2000 (Invitrogen, Carlsbad, CA) according to the manufacturer's instructions.
Rat β1Pix, β1PixDHm(L238R, L239S), β1PixSH3m(W43K), β1Pix
DH, β1PixPH, β1PixERD, β1Pix(547-586), β1Pix(587-626), β1Pix(597-616), and β1Pix(602-611) plasmids have been described (Chahdi et al., 2005; Chahdi and Sorokin, 2008). β1Pix(SH3m, DHm), β1Pix(605-608), and β1Pix(603-608) were generated using QuikChange site-directed mutagenesis kit (Stratagene, La Jolla, CA).
Mouse p66Shc cDNA cloned into pRK5-p66Shc (kindly provided by Dr. Ben Margolis, University of Michigan Medical School) was subcloned into FLAGpCMV vector (Stratagene). p66ShcS36A was generated using QuikChange site-directed mutagenesis kit. All the expression constructs were verified by DNA sequencing.
Small Interfering RNAs
pSUPER-p66Shc shRNA (5'-TGAGTCTCTGTCATCGCTG-3') was kindly provided by Dr. M. F. Lin (Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center). p66Shc small interfering RNAs (siRNAs; 5'-CGATAGTCCCACTACCCTG-3') was from Ambion (Austin, TX). Both target sequences of p66Shc siRNA were within the CH2 region.
Akt siRNA#1 (5'-TGCCCTTCTACAACCAGGA) was from Cell Signaling (Beverly, MA) and Akt siRNA#2 (5'-GGCTCCCCTCAACAACTTC-3') was from Ambion. The human βPix siRNA has been described previously (Park et al., 2004).
Immunoprecipitation and Western Analysis
HMCs were transfected with the appropriate construct for 24 h. Cells were washed twice in phosphate-buffered saline (PBS) and lysed in lysis buffer containing 20 mM Tris, pH 7.5, 100 mM NaCl, 5 mM MgCl2, 1 mM EDTA, 1% Triton X-100, 1 mM sodium fluoride, 1 mM sodium vanadate, 1 mM phenylmethylsulfonyl fluoride, 1 µg/ml pepstatin, and 1 µg/ml leupeptin. Equal amount of proteins were separated by using 7.5% SDS-PAGE, electrophoretically transferred onto a PVDF membrane (Millipore, Bedford, MA), immunoblotted with the appropriate antibody, and visualized by enhanced chemiluminescence (ECL, Amersham Pharmacia Biosciences, Piscataway, NJ). For immunoprecipitation (IP), antibodies against p66Shc (Upstate Biotechnology, Lake Placid, NY), FLAG (M2, Sigma, St. Louis, MO), or c-Myc (9E10, Santa Cruz Biotechnology, Santa Cruz, CA) were added to the cell lysate (500 µg) for a 2-h incubation, followed by addition of protein A or protein G agarose beads for an additional hour. The beads were washed three times in PBS. The immunoprecipitated proteins were released from the beads by boiling in 1x sample buffer for 5 min and subsequently were analyzed by Western blot. Total cell lysate (TCL) was run to assess the equal overexpression of the constructs. Expression of recombinant proteins was verified by immunoblotting with antibodies to the Myc or FLAG epitope tag.
Kinase inhibitors U0126 (10 µM), a MAP/ERK kinase (MEK) inhibitor, or wortmannin (100 nM), a PI-3K inhibitor, were added 4 h after cell transfection. Equal amounts of cell lysate were subjected to Western blot analysis using antibodies against phospho-S36p66Shc (Calbiochem, La Jolla, CA); phospho-ERK1/2, ERK1/2, phospho-Akt(Ser473), Akt, phospho-FOXO3a(Thr32), and FOXO3a, (Cell Signaling); p27kip1 (Santa Cruz); βPix (Chemicon, Temecula, CA); or actin (Sigma).
Cell Cycle Analysis
HMCs were seeded at a density of 12 x 104/well in six-well plates in the regular medium for 2 d and then transfected with 2 µg of empty vector, β1Pix, or β1Pix(603–608) for 48 h. Cells were trypsinized, harvested, and washed twice in PBS containing EDTA (2 mM) and BSA (0.5%). Cells were treated with 70% ethanol at 4°C overnight and then washed with PBS. The DNA of ethanol-fixed cells was stained by propidium iodide (50 µg/ml) containing DNAse-free RNase A (100 U/ml) at 4°C for 30 min. The determination of cell cycle distribution for single cells was carried out using fluorescence-activated cell sorter (FACSCalibur, Becton-Dickinson) at the MCW Flow Cytometry Core Facility.
Cell Proliferation
HMCs were counted and seeded into 96-well culture plates (6 x 103 cells/well). After 24 h, the cells were transfected with 100 ng of empty vector, β1Pix, or β1Pix(603–608) for 48 h. The cells were pulsed with 5 µCi/ml [3H]thymidine during the last 4 h of culture. Before harvesting, the cells were incubated (20 min at 37°C) with trypsin to induce detachment of the cells from the microtiter plates. The cells were washed and lysed with distilled water and collected on filters using an automatic cell harvester (Skatron, Sterling, VA). The filters were placed in ScintiSafe Econo 1 scintillation fluid (Fisher Scientific, Pittsburgh, PA) and counted with the use of a TRI-CARB 2100TR liquid scintillation counter (Packard, Meriden, CT).
Rac1 Activation Assay
Detection of GTP-Rac1 was performed by using a GST-Pak binding domain pulldown following the manufacturer's instructions (Upstate Biotechnology). Lysates from cells expressing Myc-tagged constructs β1Pix, β1PixSH3m(W43K), or β1PixDHm(L238R, L239S) were incubated with 10 µg of the Pak-PBD agarose for 60 min at 4°C and washed three times with lysis buffer, and samples were separated by SDS-PAGE and immunoblotted with anti-Rac1 antibody (Upstate Biotechnology).
Statistical Analysis
All experiments were performed in triplicate and the p values were determined using the paired Student's t test.
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RESULTS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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) and β1Pix activation (Chahdi et al., 2005). In this study, we investigated the effect of ET-1 stimulation at different time points on p66Shc and βPix expression in primary HMCs. As shown in Figure 1A, the level of βPix and p66Shc increased 12 h after ET-1 stimulation and further increased at 24 h. The effect of ET-1 stimulation was specific to p66Shc because it did not affect the levels of p46Shc or p52Shc.
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). To examine if p66Shc associates with βPix, p66Shc was first immunoprecipitated from quiescent and ET-1–treated primary HMCs using isoform-specific anti-p66Shc antibodies. Western blot analysis with anti-phospho-p66ShcSer36 showed that ET-1 induces not only an increase in p66Shc expression but also p66Shc activation after 24-h stimulation (Figure 1B). Importantly, βPix was present in this anti-p66Shc immune complex. These data taken together demonstrate that ET-1 stimulation induces the formation of βPix/p66Shc complex in vivo.
p66Shc Binding Requires β1Pix Homodimerization
Even though βPix and p66Shc are expressed in transformed HMCs, ET-1 was able to slightly increase their expression (unpublished data). The Rac1/Cdc42 guanine nucleotide exchange factor β1Pix contains central DH and PH domains and an SH3 domain located at the N-terminus. In addition, β1Pix contains a glutamic acid–rich domain (ERD, residues 511-634) within the carboxyl-terminal region. Using coimmunoprecipitation experiments in transformed HMCs, we found that endogenous βPix is associated with endogenous p66Shc (Figure 2A). This result confirms the interaction found between these proteins in primary HMCs (Figure 1B). βPix was absent when a control IgG was used instead of anti-p66Shc antibody. To characterize the p66Shc binding site in β1Pix, a series of truncated β1Pix constructs were created. We first confirmed that Myc-β1Pix was readily detected in endogenous p66Shc immunoprecipitates, but not with IgG control (unpublished data). Coimmunoprecipitation studies showed that both β1PixDH and β1PixPH bound p66Shc, whereas β1PixERD did not (Figure 2B), indicating that p66Shc binding site lies within the ERD domain of β1Pix. To further delineate the p66Shc binding site, we prepared different truncated β1Pix ERD domains, and found that deletion of amino acid 547-586 retained the ability to interact with p66Shc. No binding was observed between β1Pix(587-626) or β1Pix(597-616) and p66Shc (unpublished data). To identify the minimal p66Shc interaction sequence on β1Pix, we generated additional deletions within amino acids 597-616 of β1Pix. Our result showed that deletion of amino acids 605-608 significantly diminished the binding of p66Shc to β1Pix, whereas deletion of amino acids 603-608 or 602-611 completely abolished the ability of p66Shc to interact with β1Pix (Figure 2C). On the basis of the fact that the amino acid sequence 603-608 is located within the LZ domain, which mediates β1Pix homodimerization (Kim et al., 2001, Chahdi and Sorokin, 2008), we tested the hypothesis that the deletion of this amino acid sequence would also prevent β1Pix homodimerization. To answer this question we transfected HMC cells with Flag-β1Pix, Myc-β1Pix, or both. We found that Myc-β1Pix coimmunoprecipitated with Flag-β1Pix only when both epitope-tagged forms of β1Pix were coexpressed (Figure 2D, lane 4), confirming that β1Pix forms dimers (Kim et al., 2001, Chahdi and Sorokin, 2008). However, expression of Flag-β1Pix and Myc-β1Pix(603-608) failed to form a dimer (Figure 2D, compare lanes 4 and 5). This result indicates that p66Shc binds only to the dimeric form of β1Pix and that deletion of these residues, 603-608, is sufficient to abolish β1Pix homodimerization and p66Shc binding.
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). In this study, we investigated the effect of ET-1 stimulation at different time points on HMCs. Our results showed that ET-1 stimulation induced ERK1/2 activation at 15 min and stayed active up to 24 h as indicated by using a phospho-ERK1/2 specific antibody (Figure 3, top). Interestingly, ET-1 stimulation resulted in biphasic activation of p66Shc and FOXO3a phosphorylation. The initial increase in phosphorylation at 15 min is followed by a decrease in baselines at 4 h and subsequently by a second increase in p66Shc and FOXO3a phosphorylation. This is in contrast with the time course of Akt activation. Indeed, ET-1 induced Akt activation at 15 min and 4 h, followed by a decrease in baselines at 24 h (Figure 3). FOXO3a transcription factor, which is one of Akt substrate, was phosphorylated at 24 h, whereas Akt was completely inactive, suggesting that the second phase of FOXO3a phosphorylation induced by ET-1 is independent of Akt.
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). Total cell lysates were prepared from cells stimulated with ET-1 (100 nM) for the times indicated. Immunoblot analysis showed that the expression level of p27kip1 was elevated in quiescent HMCs and in cells treated with ET-1 for 15 min and 4 h. However, the p27kip1 protein level significantly decreased in response to ET-1 at 24 h (Figure 3, bottom). Altogether our results suggest that the second phase of ET-1-induced p66Shc phosphorylation, FOXO3a inactivation, and p27kip1 down-regulation takes place independently of Akt.
βPix Is Essential for the Second Phase of ET-1–induced p66Shc and FOXO3a Phosphorylation and p27kip1 Down-Regulation
We have shown that ET-1 increased p66Shc and βPix expression, which resulted in the formation of βPix/p66Shc complex. To examine the role of βPix in ET-1 signaling as shown above, we used βPix siRNA to knockdown endogenous βPix expression. βPix siRNA strongly suppressed βPix expression in HMCs (Figure 4A, bottom). βPix siRNA had no effect on ET-1–induced ERK1/2 activation, suggesting that ERK1/2 can be activated independently of βPix. However, depletion of βPix prevented the second phase of p66Shc and FOXO3a phosphorylation induced by ET-1 compared with cells treated with negative control siRNA (Figure 4A). βPix depletion also strongly blocked ET-1–induced p27kip1 down-regulation at 24 h.
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β1Pix-induced p66Shc Phosphorylation on Serine 36 Is ERK1/2-dependent, but Akt-independent
We have shown that βPix is essential for the second phase of phosphorylation of p66Shc and FOXO3a and for p27kip1 down-regulation induced by ET-1 by using βPix siRNA. We have also found that ET-1 induces an increase in βPix expression. Taken together these results support our hypothesis that the increase in βPix expression is responsible for the activation of the second phase in ET-1 signaling. To confirm this hypothesis the effect of β1Pix overexpression in HMCs was investigated. Using phospho-specific antibody against phosphorylated serine 36, we showed that β1Pix induced p66Shc phosphorylation, an effect that was inhibited by the MEK inhibitor U0126 but not by phosphoinositide 3-OH kinase (PI-3K) inhibitor wortmannin (Figure 5A, top). This result confirms that the second phase of p66Shc activation by ET-1 (Figure 3) or β1Pix-induced p66Shc activation does not involve Akt. We next assessed the effect of β1Pix on ERK1/2 activation using phospho-specific ERK1/2 antibody. In cells expressing β1Pix, ERK1/2 was strongly activated compared with cells transfected with empty vector (Figure 5A, bottom). Using U0126 to inhibit MEK, a kinase that directly phosphorylates and activates ERK1/2, we found that U0126 completely abolished β1Pix-mediated ERK1/2 activation, whereas PI-3K inhibitor wortmannin had no effect. Previous reports have demonstrated the role of Pak in Rac1-mediated activation of ERK1/2 (Renshaw et al., 1997; Del Pozo et al., 2000). Because it has been shown that activation of Rac1 can mediate ERK1/2 activation through Pak1-MEK1 (Frost et al., 1997; Eblen et al., 2002), we examined the ability of β1Pix to regulate Rac1 activity in HMCs. In agreement with previous reports (Park et al., 2004), cells expressing β1Pix demonstrated a marked increase in GTP-Rac1 compared with cells transfected with empty vector (Figure 5B). However, the expression of β1PixSH3m(W43K) or β1PixDHm(L238R, L239S) failed to activate Rac1. Thus the GEF activity of β1Pix mediated by the DH domain and the ability of β1Pix to bind Pak1 through its SH3 domain are essential for β1Pix-induced Rac1 activation. Next, we want to show that β1Pix-mediated Rac1 activation is necessary for ERK1/2 activation. β1Pix strongly increased ERK1/2 phosphorylation, whereas β1PixSH3m(W43K) and β1PixDHm(L238R, L239S) had only minor stimulatory effect on ERK1/2 phosphorylation (Figure 5C). In cells expressing β1Pix double mutant, β1Pix(SH3m, DHm), ERK1/2 phosphorylation was significantly decreased, indicating that both SH3 and DH domains are required for β1Pix-mediated ERK1/2 activation. Taken together, our results indicate that p66Shc phosphorylation on serine 36 is mediated by β1Pix-induced Rac1 and ERK1/2 activation. To confirm our finding, wild-type Flag-tagged p66Shc and p66ShcS36A (in which serine 36 has been mutated to alanine) were transiently cotransfected with Myc-β1Pix into HMCs. Anti-Flag immunoprecipitates demonstrate that expression of β1Pix results in p66Shc phosphorylation on serine 36. As expected, β1Pix was unable to induce phosphorylation of p66ShcS36A (Figure 5D). Cumulatively, these results demonstrate that β1Pix stimulates ERK1/2-dependent phosphorylation of p66Shc on serine 36. It must be pointed out, however, that we cannot completely exclude the presence of other phosphorylated residues on p66Shc.
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; Dijkers et al., 2000). A recent study provided compelling evidence that p66Shc serine 36 phosphorylation plays a major role in oxidative stress–induced FOXO3a inhibition (Nemoto and Finkel, 2002). Because we showed that β1Pix physically interacts with p66Shc and induces its phosphorylation on serine 36 through ERK1/2 activation, we investigated whether Akt and/or FOXO3a respond to β1Pix overexpression in HMCs. Akt phosphorylation status was not affected by β1Pix or by U0126 treatment. However, wortmannin treatment resulted in a complete inhibition of Akt phosphorylation induced by the serum present in the medium (Figure 6A, top). β1Pix induced strong FOXO3a phosphorylation compared with the cells transfected with empty vector (Figure 6A). This phosphorylation was significantly inhibited by U0126, whereas wortmannin had a less inhibitory effect. The sensitivity to wortmannin inhibition is due to the Akt-dependent FOXO3a phosphorylation induced by the presence of serum. This finding implies that activation of β1Pix signaling induces FOXO3a phosphorylation through ERK1/2-dependent but Akt-independent mechanism(s). Furthermore, β1Pix expressing cells showed a significant down-regulation of p27kip1 protein, a cyclin-dependent kinase inhibitor and a target gene for FOXO3a (Dijkers et al., 2000; Stahl et al., 2002). This down-regulation was blocked by U0126 but not by wortmannin (Figure 6A, bottom). In nontransfected cells, however, both Akt and FOXO3a phosphorylation induced by stimulation with serum were completely inhibited by wortmannin (Figure 6B, top). Moreover, wortmannin completely blocked serum-induced p27kip1 down-regulation (Figure 6B, bottom). Altogether, our results show that in HMCs β1Pix, unlike serum, induced FOXO3a phosphorylation and p27kip1 down-regulation through ERK/p66Shc-dependent but Akt-independent mechanisms. To confirm this finding, we examined the effect of Akt knockdown by RNA interference on FOXO3a phosphorylation induced by serum or β1Pix. We first confirmed that both Akt siRNAs specifically knocked down the expression of Akt (Figures 7A and 8A). Our results showed that Akt depletion by two different siRNAs strongly inhibited FOXO3a phosphorylation induced by serum (Figure 7A) but not by β1Pix (Figure 8A).
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) or with p66Shc siRNA. The cells transfected with each of p66Shc siRNAs exhibited a significant reduction in the abundance of endogenous p66Shc protein level but showed no change in the level of p46 or p52 isoforms of Shc (Figures 7B and 8B). Both p66Shc siRNAs strongly inhibited FOXO3a phosphorylation induced by β1Pix (Figure 8B) but had no effect on serum stimulation (Figure 7B), indicating that p66Shc is required for β1Pix-induced FOXO3a phosphorylation, but p66Shc is not involved in mediating serum signaling.
β1Pix/p66Shc/FOXO3a Complex Is Required for p27kip1 Down-Regulation and Cell Proliferation
The fact that endogenous βPix interacts with endogenous p66Shc and β1Pix overexpression induces FOXO3a phosphorylation raised the question of whether FOXO3a interacts with β1Pix. To assess the interaction between β1Pix and endogenous FOXO3a, lysates were obtained from cells transfected with Myc-tagged β1Pix or β1Pix homodimerization deficient mutant that cannot interact with p66Shc, β1Pix(603-608), and were immunoprecipitated with anti-myc antibody. Endogenous FOXO3a was readily detected in the immunoprecipitate, whereas deletion of amino acids 603–608 abolished the interaction between FOXO3a and β1Pix (Figure 9A). This result indicates that like p66Shc, FOXO3a binding requires β1Pix homodimerization. Anti-phospho-FOXO3a showed that FOXO3a associated with β1Pix is already phosphorylated, which may indicate a phosphorylation-dependent binding of endogenous FOXO3a to β1Pix. Furthermore, we found that endogenous FOXO3a coimmunoprecipitates with endogenous p66Shc (Figure 9B), indicating that endogenous p66Shc forms a complex with both endogenous βPix (Figure 2A) and FOXO3a.
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). β1Pix overexpression induced p27kip1 down-regulation, whereas the expression of β1Pix(603-608) unable to form β1Pix/p66Shc/FOXO3a complex blocked p27kip1 down-regulation (Figure 10A). p27kip1 is a well-known regulator of the G1/S transition through its cyclin-dependent kinase inhibitory activity, which blocks the cell in G1 phase by preventing cdk-dependent phosphorylation of pRb (Dijkers et al., 2000). The expression of β1Pix induced a strong increase in cell proliferation compared with cells transfected with empty vector as evidenced by increase in the incorporation of [3H]thymidine (Figure 10B). This increase in cell proliferation correlates with a significant increase of the percentage of cell population in the S phase of the cell cycle resulting from a decrease in the number of cells in G1 phase (Figure 10C). The expression of β1Pix routinely elicited a more than 60% increase in the cell number in S phase. The expression of β1Pix(603-608) that blocks p27kip1 down-regulation also abolished the increase in cell proliferation (Figure 10B) and reduced cell percentage in S phase of the cell cycle induced by β1Pix (Figure 10C), confirming that β1Pix plays a critical role in regulating FOXO3a transcriptional activity and cell proliferation. These findings confirm the results obtained showing that β1Pix is essential in cell proliferation induced by ET-1. Because β1Pix interacts with and activates p66Shc, we sought to determine the role of p66Shc in β1Pix signaling by examining the effect of p66Shc depletion on cell proliferation induced by β1Pix. Using two different siRNAs to knockdown p66Shc, we found that the depletion of p66Shc completely abolished β1Pix-induced cell proliferation (Figure 11). This functional link between β1Pix and p66Shc also confirms the physical interaction between these two proteins and their role in cell proliferation.
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DISCUSSION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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). Here we show that β1Pix-induced Rac1 activation requires both β1PixGEF function and SH3 domain as a Pak binding site (Figure 5B). Activation of Rac1 leads to the activation of ERK1/2 (Figure 5C) through mechanism involving Pak1 phosphorylation of MEK1 (Frost et al., 1997; Eblen et al., 2002). Activated ERK1/2 phosphorylates p66Shc (Hu et al., 2005) and mediates β1Pix-induced serine 36 phosphorylation of p66Shc (Figure 5A). βPix has been shown to induce ROS production (Park et al., 2004), resulting in p66Shc activation (Migliaccio et al., 1999; Nemoto and Finkel, 2002). In our case we could not detect any change in intracellular level of ROS in cells expressing β1Pix, and β1Pix-induced p66Shc phosphorylation was unaffected by treatment with the antioxidant ebselen (unpublished data).
The inability of β1Pix to activate Akt (Figure 6A) as well as the inability of Akt siRNAs to block β1Pix-induced FOXO3a phosphorylation (Figure 8A) indicates that Akt is not involved in β1Pix signaling. This is in agreement with our result showing that ET-1 stimulation (through βPix up-regulation) results in FOXO3a phosphorylation independently of Akt (Figure 3). However, in line with previous reports (Hu et al., 2005; Nemoto and Finkel, 2002) Akt is required for serum-stimulated FOXO3a phosphorylation and p27kip1 down-regulation (Figures 6B and 7A). In the light of this result, we explored whether ERK1/2 and p66Shc are important in mediating β1Pix effects. Blocking ERK1/2 activation (and p66Shc) inhibits both FOXO3a phosphorylation and p27kip1 down-regulation (Figure 6A). The inhibition of FOXO3a phosphorylation by p66Shc depletion (Figure 8B) confirms the importance of p66Shc in mediating FOXO3a phosphorylation, although the kinase responsible for this phosphorylation is presently unknown. Recent study showed that I
B kinase directly phosphorylates FOXO3a and promote cell proliferation (Hu et al., 2004). It is possible that FOXO3a is either directly phosphorylated by ERK1/2 or indirectly through another kinase. Interestingly, ERK1/2 has been found to form a complex with p66Shc (Hu et al., 2005). Another possibility is that Pak1, a well-characterized β1Pix effector, may phosphorylate FOXO3a. This hypothesis is supported by a previous report showing that Pak1 binds to and phosphorylates FOXO1 (Mazumdar et al., 2003). The third possibility may involve a yet unidentified kinase. Our results indicate clearly that unlike serum and ROS, β1Pix utilizes ERK/p66Shc/FOXO3a signaling pathway that does not require Akt.
Despite the lack of response to β1Pix, Akt is still active in our experimental setting and induces FOXO3a phosphorylation (Figure 6). This implies that even in β1Pix-expressing cells, FOXO3a is responsive to Akt signaling. Indeed, a pool of endogenous FOXO3a associated with β1Pix and p66Shc is already phosphorylated (Figure 9), suggesting that Akt signaling is responsible for the cytosolic localization of (phosphorylated) FOXO3a. This conclusion is further supported by the finding that Akt-independent phosphorylation mediates AFX-induced transcriptional activity and cell proliferation, whereas AFX subcellular localization is regulated by Akt (De Ruiter et al., 2001). These results are consistent with our data that disruption of β1Pix/p66Shc/FOXO3a complex induced by β1Pix(603–608) inhibits p27kip1 down-regulation, cell proliferation and cell cycle progression into S phase induced by β1Pix (Figure 10). It is interesting that both p66Shc and FOXO3a bind only to the dimeric form of β1Pix (Figure 2D), indicating that β1Pix brings p66Shc and FOXO3a together, thus providing a unique platform to regulate cell proliferation. We have recently shown that 14-3-3β binding also requires β1Pix homodimerization resulting in the modulation of its GEF activity (Chahdi and Sorokin, 2008). Therefore, we can rightly wonder whether dimerization is a general mechanism by which β1Pix interacts with all of its known partners and whether its GEF activity is affected by these interactions.
What is the role of β1Pix-induced p27kip1 down-regulation? Down-regulation of p27kip1 results in cell cycle progression into S phase. Decrease in p27kip1 protein level is found in many human cancers characterized by uncontrolled cell proliferation (Alkarian and Slingerland, 2004). Rac3, which is a downstream effector of β1Pix, is hyperactive in breast cancer cells and requires Pak to induce cell proliferation (Mira et al., 2000). Moreover, recent study showed Pak–Pix interaction to be essential for Pak activation in some breast cancer cell lines (Stofega et al., 2004). Interestingly, β1Pix expression is significantly increased in human breast cancer tissues (Ahn et al., 2003). Therefore, p27kip1 down-regulation induced by β1Pix may contribute to cell proliferation in some breast cancer cells.
It is tempting to suggest that scaffolding activity of βPix facilitates serine 36 phosphorylation of bound p66Shc because the ability of βPix and p66Shc to recruit ERK1/2 has been shown previously (Lim et al., 2003; Hu et al., 2005). Thus formation of signaling complex including βPix, ERK1/2, p66Shc, and FOXO3a is a novel signaling module that provides additional mechanistic insight into the network of signaling pathways activated by ET-1 through βPix, a molecule possessing both scaffolding and enzymatic properties. Indeed, siRNA depletion of either βPix or p66Shc clearly blocked ET-1–induced cell proliferation, demonstrating that p66Shc/βPix interaction plays an essential role in cell proliferation. The ability of ET-1 to up-regulate βPix and p66Shc expression combined with the ability of these proteins to form a complex with FOXO3a at the endogenous level further strengthens the physiological relevance of such multimolecular complex.
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ACKNOWLEDGMENTS |
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Footnotes |
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Address correspondence to: Andrey Sorokin (sorokin{at}mcw.edu)
Abbreviations used: AFX, All 1 Fused gene chromosome X; ET-1, endothelin-1; DH, Dbl homology; FOXO3a, forkhead box class O3A; GEF, guanine nucleotide exchange factor; GIT1, G protein–coupled receptor kinase (GRK)-interacting targets; LZ, leucine zipper; Pak, p21-activated kinase; β1Pix, Pak-interacting exchange factor; PH, pleckstrin homology; PKL, paxillin kinase linker; p27kip1, cyclin-dependent kinase inhibitor; SH3, Src homology 3.
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