Voltar
Artigo Acesso aberto Revisado por pares
BIBTEX RIS

The Insulin-like Growth Factor Type 1 and Insulin-like Growth Factor Type 2/Mannose-6-phosphate Receptors Independently Regulate ERK1/2 Activity in HEK293 Cells

2007; Elsevier BV; Volume: 282; Issue: 36 Linguagem: Inglês

10.1074/jbc.m703276200

ISSN

1083-351X

Autores

Hesham M. El‐Shewy, Mi‐Hye Lee, Lina M. Obeid, Ayad A. Jaffa, Louis M. Luttrell,

Tópico(s)

Pregnancy-related medical research

Resumo

Insulin-like growth factor types 1 and 2 (IGF-1; IGF-2) and insulin-like peptides are all members of the insulin superfamily of peptide hormones but bind to several distinct classes of membrane receptor. Like the insulin receptor, the IGF-1 receptor is a heterotetrameric receptor tyrosine kinase, whereas the IGF-2/ mannose 6-phosphate receptor is a single transmembrane domain protein that is thought to function primarily as clearance receptors. We recently reported that IGF-1 and IGF-2 stimulate the ERK1/2 cascade by triggering sphingosine kinasedependent "transactivation" of G protein-coupled sphingosine-1-phosphate receptors. To determine which IGF receptors mediate this effect, we tested seven insulin family peptides, IGF-1, IGF-2, insulin, and insulin-like peptides 3, 4, 6, and 7, for the ability to activate ERK1/2 in HEK293 cells. Only IGF-1 and IGF-2 potently activated ERK1/2. Although IGF-2 was predictably less potent than IGF-1 in activating the IGF-1 receptor, they were equipotent stimulators of ERK1/2. Knockdown of IGF-1 receptor expression by RNA interference reduced the IGF-1 response to a greater extent than the IGF-2 response, suggesting that IGF-2 did not signal exclusively via the IGF-1 receptor. In contrast, IGF-2 receptor knockdown markedly reduced IGF-2-stimulated ERK1/2 phosphorylation, with no effect on the IGF-1 response. As observed previously, both the IGF-1 and the IGF-2 responses were sensitive to pertussis toxin and the sphingosine kinase inhibitor, dimethylsphingosine. These data indicate that endogenous IGF-1 and IGF-2 receptors can independently initiate ERK1/2 signaling and point to a potential physiologic role for IGF-2 receptors in the cellular response to IGF-2. Insulin-like growth factor types 1 and 2 (IGF-1; IGF-2) and insulin-like peptides are all members of the insulin superfamily of peptide hormones but bind to several distinct classes of membrane receptor. Like the insulin receptor, the IGF-1 receptor is a heterotetrameric receptor tyrosine kinase, whereas the IGF-2/ mannose 6-phosphate receptor is a single transmembrane domain protein that is thought to function primarily as clearance receptors. We recently reported that IGF-1 and IGF-2 stimulate the ERK1/2 cascade by triggering sphingosine kinasedependent "transactivation" of G protein-coupled sphingosine-1-phosphate receptors. To determine which IGF receptors mediate this effect, we tested seven insulin family peptides, IGF-1, IGF-2, insulin, and insulin-like peptides 3, 4, 6, and 7, for the ability to activate ERK1/2 in HEK293 cells. Only IGF-1 and IGF-2 potently activated ERK1/2. Although IGF-2 was predictably less potent than IGF-1 in activating the IGF-1 receptor, they were equipotent stimulators of ERK1/2. Knockdown of IGF-1 receptor expression by RNA interference reduced the IGF-1 response to a greater extent than the IGF-2 response, suggesting that IGF-2 did not signal exclusively via the IGF-1 receptor. In contrast, IGF-2 receptor knockdown markedly reduced IGF-2-stimulated ERK1/2 phosphorylation, with no effect on the IGF-1 response. As observed previously, both the IGF-1 and the IGF-2 responses were sensitive to pertussis toxin and the sphingosine kinase inhibitor, dimethylsphingosine. These data indicate that endogenous IGF-1 and IGF-2 receptors can independently initiate ERK1/2 signaling and point to a potential physiologic role for IGF-2 receptors in the cellular response to IGF-2. The insulin superfamily family of peptide hormones, consisting of insulin, insulin-like growth factor type 1 (IGF-1), 2The abbreviations used are: IGFinsulin-like growth factorEGFepidermal growth factorDMSdimethylsphingosineERK1/2extracellular signal-regulated kinases 1 and 2GPCRG protein-coupled receptorINSLinsulinlike peptideIRSinsulin receptor substrateM6Pmannose-6-phosphatePMAphorbol myristate acetatePTXBordetella pertussis toxinRXFPrelaxin-family peptidesiRNAsmall interfering RNASKsphingosine kinaseS1Psphingosine-1-phosphateSCRcontrol scrambled siRNA. insulin-like growth factor type 2 (IGF-2), and the heterodimeric peptide relaxin/insulin-like factors INSL3, INSL4, INSL5, INSL6, and INSL7, regulates diverse biological functions including cell growth, differentiation, and energy balance. Because of its critical role in metabolic homeostasis, insulin signaling has long been the subject of intense investigation. By comparison, the mechanisms of action of IGF-1, IGF-2, and the more recently characterized INSLs are less thoroughly understood. insulin-like growth factor epidermal growth factor dimethylsphingosine extracellular signal-regulated kinases 1 and 2 G protein-coupled receptor insulinlike peptide insulin receptor substrate mannose-6-phosphate phorbol myristate acetate Bordetella pertussis toxin relaxin-family peptide small interfering RNA sphingosine kinase sphingosine-1-phosphate control scrambled siRNA. Although all members of the insulin superfamily share structural homology, their signals are transmitted through binding to a number of structurally dissimilar receptors. IGF-1 and IGF-2 are single chain polypeptides, with sequences 62% identical to that of proinsulin. Both contain a short D domain that is not present in insulin, and unlike insulin, they do not undergo post-translational proteolysis, such that the A and B domains remain linked in the mature peptide by a C domain analogous to the C peptide of insulin (1LeRoith D. Jr.Roberts C.T. Cancer Lett. 2003; 195: 127-137Crossref PubMed Scopus (928) Google Scholar, 2Dupont J. Holzenberger M. Birth Defects Res. 2003; 69: 257-271Crossref PubMed Scopus (165) Google Scholar). IGF-1 and IGF-2 bind two structurally distinct types of receptor, referred to as the IGF-1 and IGF-2/mannose-6-phosphate (M6P) receptors. The IGF-1 receptor is heterotetrameric transmembrane receptor tyrosine kinase that is structurally and functionally related to the insulin receptor. It is composed of two extracellular α-subunits that contain the ligand-binding domain and two transmembrane β-subunits that possess intrinsic ligand-stimulated tyrosine kinase activity (3LeRoith D. Werner H. Beitner-Johnson D. Jr.Roberts C.T. Endocr. Rev. 1995; 16: 143-163Crossref PubMed Scopus (1251) Google Scholar, 4Baserga R. Hongo A. Rubini M. Prisco M. Valentinis B. Biochim. Biophys. Acta. 1997; 1332: F105-F126Crossref PubMed Scopus (487) Google Scholar). Ligand binding to the α-subunit activates the β-subunit tyrosine kinase, resulting in tyrosine phosphorylation of intracellular adapter proteins, such as insulin receptor substrate (IRS)-1 and IRS-2, Shc, and Gab1 (5Wang L.M. Jr.Myers M.G. Sun X.J. Aaronson S.A. White M.F. Pierce J.H. Science. 1993; 261: 1591-1594Crossref PubMed Scopus (371) Google Scholar, 6White M.F. Khan C.R. J. Biol. Chem. 1994; 269: 1-4Abstract Full Text PDF PubMed Google Scholar, 7Janez A. Worrall D.S. Imamura T. Sharma P.M. Olefsky J.M. J. Biol. Chem. 2000; 275: 26870-26876Abstract Full Text Full Text PDF PubMed Google Scholar). These adapters, in turn, provide docking sites for catalytically active proteins such as Grb2/mSos, which catalyzes Ras activation, and the p85 regulatory subunit of phosphatidylinositol 3-kinase α, which activates Akt and promotes cell survival via suppression of the Bcl2-antagonist of cell death (BAD)/Bcl-X apoptotic pathway (8del Peso L. Gonzalez-Garcia M. Page C. Herrera R. Nunez G. Science. 1997; 278: 687-689Crossref PubMed Scopus (1987) Google Scholar, 9Franke T.F. Kaplan D.R. Cantley L.C. Cell. 1988; 88: 435-437Abstract Full Text Full Text PDF Scopus (1522) Google Scholar). Both IGF-1 and IGF-2 bind the IGF-1 receptor, albeit with different affinity, and most of their biological activities have been ascribed to activation of the IGF-1 receptor. Unlike the IGF-1 receptor, the IGF-2/M6P receptor is a type 1 single transmembrane glycoprotein composed of a large extracellular domain made up of 15 homologous cysteine-rich repeats, a single transmembrane region, and a short carboxylterminal cytoplasmic tail (10Kornfeld S. Annu. Rev. Biochem. 1992; 61: 307-330Crossref PubMed Scopus (934) Google Scholar, 11Ghosh P. Dahms N.M. Kornfeld S. Nat. Rev. Mol. Cell Biol. 2003; 4: 202-212Crossref PubMed Scopus (801) Google Scholar, 12Hassan A.B. Am. J. Pathol. 2003; 162: 3-6Abstract Full Text Full Text PDF PubMed Scopus (37) Google Scholar). It localizes primarily to the trans-Golgi network and endosomal compartments, and to a lesser extent, on the cell surface. Binding of IGF-2- and M6P-containing ligands occurs at two distinct sites, with repeats 3 and 9 involved in binding proteins bearing M6P moieties and repeat 11 containing the core IGF-2-binding sites (3LeRoith D. Werner H. Beitner-Johnson D. Jr.Roberts C.T. Endocr. Rev. 1995; 16: 143-163Crossref PubMed Scopus (1251) Google Scholar, 13Braulke T. Horm. Metab. Res. 1999; 31: 242-246Crossref PubMed Scopus (135) Google Scholar). Lacking intrinsic catalytic activity, the IGF-2/M6P receptor is thought to function primarily as a "clearance receptor," with known roles in the internalization, lysosomal trafficking, degradation of IGF-2, proliferin, and glycosylated leukemia inhibitory factor (10Kornfeld S. Annu. Rev. Biochem. 1992; 61: 307-330Crossref PubMed Scopus (934) Google Scholar, 14Lee S.-J. Nathans D. J. Biol. Chem. 1988; 263: 3521-3527Abstract Full Text PDF PubMed Google Scholar, 15Hawkes C. Kar S. J. Comp. Neurol. 2003; 458: 113-127Crossref PubMed Scopus (52) Google Scholar), and proteolytic activation of latent transforming growth factor-β (16Purchio A.F. Cooper J.A. Brunner A.M. Lioubin M.N. Gentry L.E. Kovacina K.S. Roth R.A. Marqardt H. J. Biol. Chem. 1988; 263: 14211-14215Abstract Full Text PDF PubMed Google Scholar, 17Dennis P.A. Rifkin D.B. Proc. Natl. Acad. Sci. U. S. A. 1991; 88: 580-584Crossref PubMed Scopus (460) Google Scholar). It is less clear whether IGF-2/M6P receptors initiate transmembrane signals. Endothelial cell migration and angiogenesis in response to the placental angiogenic hormone, proliferin, is reportedly IGF-2/M6P receptor-dependent (18Groskopf J.C. Syu L.J. Saltiel A.R. Linzer D.I. Endocrinology. 1997; 138: 2835-2840Crossref PubMed Scopus (65) Google Scholar). Although some reports suggest that it plays a role in IGF-2 signaling (19Braulke T. Tippmer S. Neher E. von Figura K. EMBO J. 1989; 8: 681-686Crossref PubMed Scopus (57) Google Scholar, 20Jones J.I. Clemmons D.R. Endocr. Rev. 1995; 16: 3-34Crossref PubMed Google Scholar), the prevailing opinion is that the biological effects of IGF-2 are predominantly mediated through the IGF-1 receptor or insulin receptor isoform A (21Werner H. LeRoith D. Adv. Cancer Res. 1996; 68: 183-223Crossref PubMed Google Scholar, 22Frasca F. Pandini G. Scalia P. Sciacca L. Mineo R. Costantino A. Goldfine I.D. Belfiore A. Vigneri R. Mol. Cell Biol. 1999; 19: 3278-3288Crossref PubMed Scopus (723) Google Scholar, 23Hawkes C. Kar S.J. Brain Res. Rev. 2004; 44: 117-140Crossref PubMed Scopus (124) Google Scholar). At least some of the recently characterized relaxin/insulinlike factors bind yet another class of membrane receptor, seven membrane-spanning G protein-coupled receptors (GPCRs). INSLs are composed of two peptide chains connected by three disulfide bonds and share a high degree of structural homology with insulin (24Lok S. Biol. Reprod. 2000; 62: 1593-1599Crossref PubMed Scopus (100) Google Scholar, 25Liu C. J. Biol. Chem. 2003; 278: 50765Abstract Full Text Full Text PDF PubMed Scopus (208) Google Scholar, 26Bartsch O. Bartlick B. Ivell R. Mol. Human Reprod. 2001; 7: 799-809Crossref PubMed Scopus (95) Google Scholar). Based on this structural similarity, it was initially thought that INSLs would signal by binding to receptor tyrosine kinases, similar to the insulin and IGF receptors. Recently, however, it has been shown that relaxin activates a family of leucine-rich repeat-containing GPCRs, the relaxin family peptide (RXFP) receptors, previously known as LGRs, and mediates heterotrimeric G protein-dependent activation of a number of effectors including adenylyl cyclase (26Bartsch O. Bartlick B. Ivell R. Mol. Human Reprod. 2001; 7: 799-809Crossref PubMed Scopus (95) Google Scholar, 27Hsu S.Y. Nakabayashi K. Nishi S. Kumagai J. Kudo M. Sherwood O.D. Hsueh A.J.W. Science. 2002; 295: 671-674Crossref PubMed Scopus (681) Google Scholar, 28Silvertown J.D. Int. J. Cancer. 2003; 107: 513-519Crossref PubMed Scopus (65) Google Scholar, 29Wilkinson T.N. Speed T.P. Tregear G.W. Bathgate R.A. BMC Evol. Biol. 2005; 5: 14-31Crossref PubMed Scopus (166) Google Scholar, 30Bathgate R.A. Ivell R. Sanborn B.M. Sherwood O.D. Summers R.J. Pharmacol. Rev. 2006; 58: 7-31Crossref PubMed Scopus (272) Google Scholar). Although insulin and IGF-1/2 do not appear to activate RXFP receptors to any significant extent, these results clearly broaden the signaling repertoire of peptides with homology to insulin. We recently reported that in HEK293 cells, exposure to IGF-1 or IGF-2 leads to activation of the ERK1/2 mitogen-activated protein (MAP) kinase cascade through a mechanism involving sphingosine kinase (SK)-dependent "transactivation" of G protein-coupled sphingosine-1-phosphate (S1P) receptors (31El-Shewy H.M. Johnson K.R. Lee M.-H. Jaffa A.A. Obeid L.M. Luttrell L.M. J. Biol. Chem. 2006; 281: 31399-31407Abstract Full Text Full Text PDF PubMed Scopus (71) Google Scholar). Here, we sought to definitively identify the endogenous receptor(s) that mediate G protein-dependent ERK1/2 activation in response to IGF-1 and IGF-2 in HEK293 cells. Through selective silencing of IGF-1 and IGF-2/M6P receptor expression, we find that although activation of the IGF-1 receptor is sufficient to account for the response to IGF-1, activation of ERK1/2 by IGF-2 occurs in large part through the IGF-2/M6P, independent of IGF-1 receptor expression. These data suggest that both IGF-1 and IGF-2/M6P receptors play a physiologic role in the cellular response to IGFs and suggest that SK-dependent S1P receptor transactivation might serve as a general mechanism of heterotrimeric G protein-dependent signaling by multiple classes of non-GPCR. Materials—Tissue culture medium, fetal bovine serum, and penicillin/streptomycin were from Invitrogen. Insulin-like peptides INSL3, INSL4, INSL6, and INSL7 were from Phoenix Pharmaceuticals (Belmont, CA). IGF-1, IGF-2, and phorbol 12-myristate 13-acetate (PMA) were from Sigma. Double-stranded small interfering (si)RNAs were purchased from Ambion (Austin, TX). GeneSilencer™ transfection reagent was from Gene Therapy Systems (San Diego, CA). Primers for real-time PCR were from Integrated DNA Technologies (Coralville, IA). RNeasy kits were from Qiagen Corp. (Valencia, CA), and iScript cDNA synthesis kits and iQ™ SYBR® Green Supermix kits were from Bio-Rad Laboratories. Pertussis toxin was from List Biological Laboratories (Campbell, CA). S1P and dimethylsphingosine (DMS) were provided by the Medical University of South Carolina (MUSC) Lipidomics Core (Department of Biochemistry, MUSC, Charleston, SC). Goat polyclonal anti-IGF-1 receptor (Ab-2) and anti-IGF-1 receptor phospho-Tyr1158 were from Calbiochem. Mouse monoclonal anti-human CD222 M6P/IGF2R was from Novus Biologicals (Littleton, CO). Rabbit polyclonal anti-ERK1/2 and phospho-ERK1/2 IgG were from Cell Signaling Technology (Beverly, MA). Horseradish peroxidase-conjugated donkey anti-rabbit IgG was from Amersham Biosciences. Cell Culture—HEK293 cells were obtained from the American Type Culture Collection and maintained in minimum essential medium supplemented with 10% fetal bovine serum and penicillin/streptomycin. siRNA Down-regulation of IGF-1 and IGF-2 Receptor Expression—IGF-1 receptor expression was down-regulated using human IGF-1 receptor sequence-specific validated siRNA (vendor ID number 74). Down-regulation of IGF-2 receptor was performed by targeting two different sites located 657 and 2050 nucleotides downstream of the start codon using sequence-specific siRNAs (5′-GGAGGUGCCAUGCUAUGUGtt-3′ and 5′-CACAUAGCAUGGCACCUCCtt-3′) for the first site and sequence-specific siRNAs (5′-GGGUUUUCUUUUGACUUAUtt-3′ and 5′-AUAAGUCAAAAGAAAACCCtg-3′) for the second site. Scrambled siRNA sequences (5′-ACGUGACACGUUCGGAGAAAdTdT-3′ and 5′-UUCUCCGAACGUGUCACGUdTdT-3′) were used as negative controls. HEK293 cells were seeded in collagen-coated 10-cm dishes at a density of 2 × 105 cells/dish 24 h before transfection. Cells were transfected using Gene Silencer® siRNA transfection reagent according to the manufacturer's protocol. 24 h after transfection, cells were split into multiwell plates, as appropriate, and serum-deprived overnight in growth medium supplemented with 0.5% bovine serum albumin and 10 mm HEPES, pH 7.4, prior to stimulation. The efficiency of the knockdown was determined by quantitative real-time PCR for receptor mRNA and immunoblotting for IGF-1 and IGF-2 receptor protein 48 h after transfection. Quantitative Real-time PCR—Total cellular RNA was isolated using the RNeasy kit according to the manufacturer's instructions. cDNA was prepared from 1 μg of total RNA with A260/A280 > 1.8 using the iScript cDNA synthesis kit per the manufacturer's instructions. Quantitative real-time PCR was performed with an iCycler 1Q real-time detection system using the iQ™ SYBR® Green Supermix kit. Reactions were performed using specific primers. For IGF-1 receptor, the forward primer was 5′-GCACCATCTTCAAGGGCAATTTG-3′, and the reverse primer 5′-AGGAAGGACAAGGAGACCAAGG-3′; for IGF-2R receptor, the forward primer 5′-GAGGGAAGAGGCAGGAAAG-3′, and the reverse primer was 5′-TGTGGCAGGCATACTCAG-3′; and for β-actin, the forward primer was 5′-ATTGGCAATGAGCGGTTCC-3′, and the reverse primer was 5′-GGTAGTTTCGTCGATGCCACA-3′. Realtime PCR results were analyzed using Softmax® Pro software (Molecular Devices Corp.). IGF-1 and IGF-2 receptor mRNA abundance was normalized to β-actin as an endogenous control. Protein Immunoblotting—Appropriately transfected HEK293 cells were split to collagen-coated 12-well plates, serum-deprived overnight, and preincubated in the presence or absence of inhibitors as described in the figure legends. Agonist stimulations were for 10 min, after which monolayers were washed once in 4 °C phosphate-buffered saline and lysed in 200 μlof Laemmli sample buffer. Samples containing 20 μg of cell protein were resolved by SDS-PAGE and transferred to polyvinylidene difluoride membrane for immunoblotting. Proteins were detected with polyclonal IgG against ERK1/2, phospho-ERK1/2, IGF-1 receptor, or IGF-1 receptor pY1158 as appropriate, with horseradish peroxidase-conjugated polyclonal donkey anti-rabbit IgG as secondary antibody. For immunoblotting, the IGF-2/M6P receptor, mouse monoclonal anti-human M6P/IGF2R IgG, was used, with horseradish peroxidase-conjugated anti-mouse IgG as secondary antibody. Total ERK1/2 was measured to confirm equal loading of the whole cell lysate samples. Immune complexes were visualized by enzyme-linked chemiluminescence and quantified using a Fluor-S MultiImager. IGF-1 and IGF-2, but Not Insulin or INSLs, Potently Activate ERK1/2 in HEK293 Cells—Insulin superfamily peptides interact with several classes of membrane receptor, and in some cases, a single peptide can bind to more than one receptor type. This is particularly the case for insulin, IGF-1 and IGF-2, each of which can bind to the IGF-1, IGF-2, and insulin receptors (1LeRoith D. Jr.Roberts C.T. Cancer Lett. 2003; 195: 127-137Crossref PubMed Scopus (928) Google Scholar, 2Dupont J. Holzenberger M. Birth Defects Res. 2003; 69: 257-271Crossref PubMed Scopus (165) Google Scholar, 32Dupont J. LeRoith D. Horm. Res. 2001; 55: 22-36Crossref PubMed Scopus (173) Google Scholar, 33Adams T.E. Epa V.C. Garrett T.P. Ward C.W. CMLS Cell. Mol. Life Sci. 2000; 57: 1050-1093Crossref PubMed Scopus (484) Google Scholar). Therefore, we initially tested a panel of insulin-like peptides for the ability to activate ERK1/2 in HEK293 cells. As shown in Fig. 1, IGF-1 and IGF-2 both potently activated endogenous ERK1/2, although IGF-1 was somewhat more efficacious at maximal concentrations. Insulin elicited a response only at high concentrations, consistent with effects mediated by low affinity binding to IGF-1 receptors (34Sasaoka T. Draznin B. Leitner J.W. Langlois W.J. Olfesky J.M. J. Biol. Chem. 1994; 269: 10734-10738Abstract Full Text PDF PubMed Google Scholar, 35Sasaoka T. Rose D.W. Jhun B.H. Saltiel A.R. Draznin B. Olfesky J.M. J. Biol. Chem. 1994; 269: 13689-13694Abstract Full Text PDF PubMed Google Scholar, 36Roudabush F.L. Pierce K.L. Maudsley S. Khan K.D. Lin F.-T. Luttrell L.M. J. Biol. Chem. 2000; 275: 22583-22589Abstract Full Text Full Text PDF PubMed Scopus (233) Google Scholar). The INSLs tested, INSL3, INSL4, INSL6, and INSL7, were inactive even at high concentrations, indicating that the G protein-coupled RXFP receptors are either not expressed or not coupled to ERK1/2 activation in this cell line. Since both IGF-1 and IGF-2 can activate the IGF-1 receptor tyrosine kinase, we next compared the EC50 for IGF-1- and IGF-2-stimulated IGF-1 receptor activation with the EC50 of each for ERK1/2 activation. As shown in Fig. 2, IGF-2 was as efficacious but 2.3-fold less potent than IGF-1 at stimulating tyrosine autophosphorylation of the IGF-1 receptor β-subunit. This is consistent with the reported lower affinity of IGF-2 binding to the IGF-1 receptor (32Dupont J. LeRoith D. Horm. Res. 2001; 55: 22-36Crossref PubMed Scopus (173) Google Scholar, 33Adams T.E. Epa V.C. Garrett T.P. Ward C.W. CMLS Cell. Mol. Life Sci. 2000; 57: 1050-1093Crossref PubMed Scopus (484) Google Scholar). In contrast, IGF-1 and IGF-2 were equipotent activators of ERK1/2, with EC50 values of 11.0 and 11.8 nm, respectively. This apparent discrepancy prompted us to consider the possibility that IGF-2 might mediate ERK1/2 activation through another receptor, particularly when present at concentrations that produced submaximal IGF-1 receptor activation. Down-regulating IGF-1 and IGF-2/M6P Receptors Has Differential Effects on IGF-1- and IGF-2-stimulated ERK1/2 Activation—To test the hypothesis that both IGF-1 and IGF-2/M6P receptors played a role in IGF-mediated ERK1/2 activation, we employed RNA interference to down-regulate endogenous receptor expression singly and in combination and determined the effect on the ability of IGF-1 and IGF-2 to activate ERK1/2. These assays employed concentrations of IGF-1 and IGF-2 (10 nm) that approximated the EC50 for ERK1/2 activation, at which concentration IGF-2 was less effective than IGF-1 at activating the IGF-1 receptor. Fig. 3, A and B, shows the effects of optimal IGF-1 receptor down-regulation (75 nm siRNA; 48 h after transfection). When compared with cells transfected with scrambled control siRNA, IGF-1 receptor mRNA levels measured by quantitative reverse transcription-PCR were reduced by 84%, which corresponded with an 87% reduction in receptor protein measured by immunoblot. As shown in Fig. 3C, down-regulation of IGF-1 receptors reduced IGF-1- and IGF-2-stimulated IGF-1 receptor β-subunit phosphorylation by about 90%, proportional to the reduction in receptor level. As shown in Fig. 3D, IGF-1 receptor down-regulation significantly reduced ERK1/2 activation by both IGF-1 and IGF-2. As a percentage of the agonist-induced increase in ERK1/2 phosphorylation, the IGF-1 response was reduced by 77%, whereas the IGF-2 response decreased by 64%. Although these data clearly indicate that both IGF-1 and IGF-2 can engage the ERK1/2 cascade through the IGF-1 receptor, the finding that the IGF-2 response was less dependent upon IGF-1 receptor expression led us to test whether the IGF-2/M6P receptor also played a role in the response. Fig. 4 shows the effects of an identical set of experiments performed under conditions of IGF-2/M6P receptor down-regulation. As shown in Fig. 4, A and B, optimal IGF-2/M6P receptor down-regulation (100 nm siRNA; 48 h) reduced IGF-2/M6P receptor mRNA and protein levels by 74 and 83%, respectively. Under these conditions, there was no change in the level of IGF-1 receptor expression or, as shown in Fig. 3C, IGF-stimulated phosphorylation of the IGF-1 receptor β-subunit. IGF-1-stimulated ERK1/2 activation was unaffected by IGF-2/M6P receptor down-regulation. In striking contrast, IGF-2-stimulated ERK1/2 activation was reduced by 74%. Since the ability of IGF-2 to activate the IGF-1 receptor was unchanged in IGF-2/M6P receptor knockdown cells (Fig. 3C), the loss of signal probably represents loss of a direct IGF-2/M6P receptor-mediated signal and not decreased delivery of IGF-2 to the IGF-1 receptor. Fig. 5 shows the effects of simultaneous down-regulation of both the IGF-1 and the IGF-2/M6P receptors. As shown in Fig. 5, A and B, simultaneous transfection of IGF-1 and IGF-2/M6P receptor siRNAs down-regulated both receptors to a degree comparable with that achieved in the individual siRNA transfections. When compared with cells treated with scrambled control siRNA, IGF-1 and IGF-2/M6P mRNA levels were reduced by 88 and 84%, respectively, with a 90% reduction in the expression of each receptor. Fig. 5C confirms that a comparable reduction in IGF-1- and IGF-2-stimulated IGF-1 receptor β-subunit phosphorylation was achieved. As shown in Fig. 5D, when both the IGF-1 and the IGF-2/M6P receptors were down-regulated simultaneously, the reduction in IGF-1-stimulated ERK1/2 activation was 86%, which was not significantly different from the 77% reduction achieved by IGF-1 receptor knockdown alone. In contrast, IGF-2-stimulated ERK1/2 activation was abolished when both receptors were down-regulated. The effects of down-regulating IGF-1 and IGF-2/M6P receptor expression on IGF-1- and IGF-2-stimulated ERK1/2 activation are summarized in Fig. 6. As shown in Fig. 6A, only IGF-1 receptor down-regulation affected IGF-1-stimulated ERK1/2 activation, and the degree of inhibition correlated closely with the extent of IGF-1 receptor knockdown. This result supports the conclusion that in HEK293 cells, the effects of IGF-1 are mediated almost exclusively through binding to the IGF-1 receptor tyrosine kinase. In contrast, IGF-2-stimulated ERK1/2 activation was partially inhibited when either the IGF-1 or the IGF-2/M6P receptor was down-regulated independently and eliminated only when the two receptors were down-regulated together. These data support the conclusion that IGF-2 signals in part by binding to the IGF-1 receptor but also by binding to the IGF-2/M6P receptor. Moreover, the response mediated by the IGF-2/M6P receptor is independent of IGF-1 receptor since Fig. 4C clearly demonstrates that down-regulating IGF-2/M6P receptors has no effect on the ability of IGF-2 to activate the IGF-1 receptor. IGF-1 and IGF-2/M6P Receptors Employ a Common Sphingosine Kinase-dependent Mechanism to Regulate ERK1/2 Activity—We recently demonstrated that IGFs can activate ERK1/2 through a novel mechanism involving SK-dependent transactivation of heterotrimeric G protein-coupled S1P receptors (31El-Shewy H.M. Johnson K.R. Lee M.-H. Jaffa A.A. Obeid L.M. Luttrell L.M. J. Biol. Chem. 2006; 281: 31399-31407Abstract Full Text Full Text PDF PubMed Scopus (71) Google Scholar). To determine whether signals transmitted via the IGF-1 and IGF-2/M6P receptors employed the same or different mechanisms, we exposed HEK293 cells to EC50 concentrations of IGF-1 or IGF-2 in the presence or absence of either DMS, an inhibitor of SK activity, or pertussis toxin (PTX), which inactivates Gi/o family heterotrimeric G proteins. As shown in Fig. 7A, DMS treatment eliminated both IGF-1-stimulated and IGF-2-stimulated ERK1/2 phosphorylation, consistent with a requirement for SK activity in the action of both receptors. ERK1/2 activation in response to S1P was unaffected, confirming that the DMS-sensitive step in the pathway was upstream of the S1P receptor. ERK1/2 activation by PMA, which causes protein kinase C-dependent ERK1/2 activation at the level of c-Raf1 (37Kolch W. Heidecker G. Kochs G. Hummel R. Vahidi H. Mischak H. Finkenzeller G. Marme D. Rapp U.R. Nature. 1993; 364: 249-252Crossref PubMed Scopus (1159) Google Scholar), was likewise unaffected. Fig. 7B shows the effects of PTX on IGF-stimulated ERK1/2 activation. Consistent with our previous observations (31El-Shewy H.M. Johnson K.R. Lee M.-H. Jaffa A.A. Obeid L.M. Luttrell L.M. J. Biol. Chem. 2006; 281: 31399-31407Abstract Full Text Full Text PDF PubMed Scopus (71) Google Scholar, 38Luttrell L.M. van Biesen T. Hawes B.E. Koch W.J. Touhara K. Lefkowitz R.J. J. Biol. Chem. 1995; 270: 16495-16498Abstract Full Text Full Text PDF PubMed Scopus (189) Google Scholar), pretreatment with PTX inhibited IGF-1-, IGF-2-, and S1P-stimulated ERK1/2 phosphorylation by 47, 66, and 73%, respectively. PMA-stimulated ERK1/2 activation was not affected. The incomplete inhibition produced by PTX probably results from coupling of S1P receptors to PTX-insensitive Gq/11 family heterotrimeric G proteins in addition to Gi/o family G proteins since we have observed that PTX and a Gq/11 inhibitor peptide additively inhibit S1P-stimulated ERK1/2 activation in HEK293 cells (31El-Shewy H.M. Johnson K.R. Lee M.-H. Jaffa A.A. Obeid L.M. Luttrell L.M. J. Biol. Chem. 2006; 281: 31399-31407Abstract Full Text Full Text PDF PubMed Scopus (71) Google Scholar, 39Akhter S.A. Luttrell L.M. Rockman H.A. Lefkowitz R.J. Koch W.J. Science. 1998; 280: 574-577Crossref PubMed Scopus (393) Google Scholar). Collectively, these data suggest that two distinct receptor types, the IGF-1 receptor tyrosine kinase and the catalytically inactive IGF-2/M6P receptor, share a common mechanism of intracellular signaling involving SK-dependent transactivation of S1P receptors. Having recently found that IGFs can initiate heterotrimeric G protein-dependent signals by a mechanism involving SK activation and S1P-dependent transactivation of G protein-coupled S1P receptors (31El-Shewy H.M. Johnson K.R. Lee M.-H. Jaffa A.A. Obeid L.M. Luttrell L.M. J. Biol. Chem. 2006; 281: 31399-31407Abstract Full Text Full Text PDF PubMed Scopus (71) Google Scholar), the major goal of this study was to determine which receptor(s) mediate the response. The insulin superfamily of peptides binds a structurally diverse cadre of receptors, including receptor tyrosine kinases; the insulin and IGF-1 receptors, a non-catalytic type 1 transmembrane receptor; the IGF-2/M6P receptor and several heptahelical GPCRs; and the RXFP receptors. Therefore, we first tested a broad panel of insulin family peptides for the ability to activate ERK1/2 in untransfected HEK293 cells. Although both IGF-1 and IGF-2 potently activated ERK1/2, the RXFP ligands, INSL3, INSL4, INSL6, and INSL7, did not. Consistent with published reports that despite structural homology, insulin, IGF-1, and IGF-2 do not activate RXFPs (26Bartsch O. Bartlick B. Ivell R. Mol. Human Reprod. 2001; 7: 799-809Crossref PubMed Scopus (95) Google Scholar, 27Hsu S.Y. Nakabayashi K. Nishi S. Kumagai J. Kudo M. Sherwood O.D. Hsueh A.J.W. Science. 2002; 295: 671-674Crossref PubMed Scopus (681) Google Scholar, 28Silvertown J.D. Int. J. Cancer. 2003; 107: 513-519Crossref PubMed Scopus (65) Google Scholar, 29Wilkinson T.N. Speed T.P. Tregear G.W. Bathgate R.A. BMC Evol. Biol. 2005; 5: 14-31Crossref PubMed Scopus (166) Google Scholar, 30Bathgate R.A. Ivell R. Sanborn B.M. Sherwood O.D. Summers R.J. Pharmacol. Rev. 2006; 58: 7-31Crossref PubMed Scopus (272) Google Scholar), our results indicate that IGF-1 and IGF-2 do not cause G protein-dependent ERK1/2 activation by binding directly to a known GPCR. We next employed siRNA down-regulation of IGF-1 and IGF-2/M6P receptor expression to assign the IGF-1 and IGF-2 responses to one or more specific receptors. Predictably, we found that IGF-1 receptors are activated by both IGF-1 and IGF-2, albeit with different potency, and that IGF-1 receptors contribute to ERK1/2 activation in response to both ligands. Surprisingly, we found that down-regulating the IGF-2/M6P receptor selectively inhibited the response to IGF-2 but not IGF-1. Loss of IGF-2/M6P receptors had no effect on the ability of IGF-2 to activate the IGF-1 receptor, indicating that the IGF-2/M6P receptor was not acting simply to deliver IGF-2 to the cell surface. Furthermore, the effects of IGF-1 and IGF-2/M6P receptor down-regulation on IGF-2-stimulated ERK1/2 activation were approximately additive, strongly suggesting that these two structurally distinct receptors independently contribute to IGF-2 signaling in HEK293 cells. The most accepted function of the IGF-2/M6P receptor is in the cellular uptake and degradation of peptides such as IGF-2, proliferin, and leukemia inhibitory factor (10Kornfeld S. Annu. Rev. Biochem. 1992; 61: 307-330Crossref PubMed Scopus (934) Google Scholar, 14Lee S.-J. Nathans D. J. Biol. Chem. 1988; 263: 3521-3527Abstract Full Text PDF PubMed Google Scholar, 15Hawkes C. Kar S. J. Comp. Neurol. 2003; 458: 113-127Crossref PubMed Scopus (52) Google Scholar). It also plays a role in the uptake and proteolytic activation of latent transforming growth factor-β (16Purchio A.F. Cooper J.A. Brunner A.M. Lioubin M.N. Gentry L.E. Kovacina K.S. Roth R.A. Marqardt H. J. Biol. Chem. 1988; 263: 14211-14215Abstract Full Text PDF PubMed Google Scholar, 17Dennis P.A. Rifkin D.B. Proc. Natl. Acad. Sci. U. S. A. 1991; 88: 580-584Crossref PubMed Scopus (460) Google Scholar). Nonetheless, some data support a role for the IGF-2/M6P receptor in IGF-2 signaling (19Braulke T. Tippmer S. Neher E. von Figura K. EMBO J. 1989; 8: 681-686Crossref PubMed Scopus (57) Google Scholar, 20Jones J.I. Clemmons D.R. Endocr. Rev. 1995; 16: 3-34Crossref PubMed Google Scholar). In rhabdomyosarcoma cells, IGF-2 stimulates cell migration, apparently by binding the IGF-2/M6P receptor (40Minniti C.P. Kohn E.C. Grubb J.H. Sly W.S. Oh Y. Muller H.L. Rosenfeld R.G. Helman L.J. J. Biol. Chem. 1992; 267: 9000-9004Abstract Full Text PDF PubMed Google Scholar). Certain in vitro effects of IGF-2, such as stimulating Ca2+ influx and DNA synthesis in 3T3 fibroblasts (41Nishimoto I. Murayama Y. Katada T. Ui M. Ogata E. J. Biol. Chem. 1989; 264: 14029-14038Abstract Full Text PDF PubMed Google Scholar, 42Murayama Y. Okamoto T. Ogata E. Asano T. Iiri T. Katada T. Ui M. Grubb J.H. Sly W.S. Nishimoto I. J. Biol. Chem. 1990; 265: 17456-17462Abstract Full Text PDF PubMed Google Scholar), have been attributed to activation of heterotrimeric G proteins by the IGF-2/M6P receptor (43Nishimoto I. Hata Y. Ogata E. Kojima I. J. Biol. Chem. 1987; 262: 12120-12126Abstract Full Text PDF PubMed Google Scholar, 44Kojima I. Nishimoto I. Iiri T. Ogata E. Rosenfeld R. Biochem. Biophys. Res. Commun. 1988; 154: 9-19Crossref PubMed Scopus (47) Google Scholar). More recently, Leu27IGF-2, which binds preferentially to the IGF-2/M6P receptor, has been shown to stimulate pertussis toxin-sensitive, protein kinase C-dependent, protein phosphorylation and modulate central cholinergic receptor function (45Hawkes C. Jhamandas J.H. Harris K.H. Fu W. MacDonald R.G. Kar S. J. Neurosci. 2006; 26: 585-596Crossref PubMed Scopus (71) Google Scholar). However, previous attempts to ascribe specific signaling functions to the IGF-2/M6P receptor have been hampered by the fact that IGF-2 also binds and activates the IGF-1 receptor tyrosine kinase. Indeed, several authors have suggested that the biological effects of IGF-2 are mediated through the IGF-1 receptor or insulin receptor isoform A (21Werner H. LeRoith D. Adv. Cancer Res. 1996; 68: 183-223Crossref PubMed Google Scholar, 22Frasca F. Pandini G. Scalia P. Sciacca L. Mineo R. Costantino A. Goldfine I.D. Belfiore A. Vigneri R. Mol. Cell Biol. 1999; 19: 3278-3288Crossref PubMed Scopus (723) Google Scholar, 23Hawkes C. Kar S.J. Brain Res. Rev. 2004; 44: 117-140Crossref PubMed Scopus (124) Google Scholar). In our study, we find that down-regulation of IGF-2/M6P receptors leads to a marked reduction in IGF-2-stimulated, but not IGF-1-stimulated, ERK1/2 activation, consistent with signaling directly via the IGF-2/M6P receptor. Our results also indicate that IGF-1, acting via the IGF-1 receptor, and IGF-2, acting via both the IGF-1 and the IGF-2/M6P receptors, employ a common heterotrimeric G protein-dependent mechanism to activate ERK1/2. We have previously shown that both IGF-1 and IGF-2 promote membrane translocation and activation of SK1, increase intracellular and extracellular S1P levels, and activate G protein-coupled S1P receptors in HEK293 cells (31El-Shewy H.M. Johnson K.R. Lee M.-H. Jaffa A.A. Obeid L.M. Luttrell L.M. J. Biol. Chem. 2006; 281: 31399-31407Abstract Full Text Full Text PDF PubMed Scopus (71) Google Scholar). What remains unclear is how these two structurally distinct receptors activate SK. In vitro studies have shown that SK1 has high affinity for lipid bilayers rich in phosphatidylserine and that conserved Thr54 and Asn89 residues in the putative membrane-binding surface of the protein are necessary for membrane binding in vitro and in cells (46Stahelin R.V. Hwang J.H. Kim J.H. Park Z.Y. Johnson K.R. Obeid L.M. Cho W. J. Biol. Chem. 2005; 280: 43030-43038Abstract Full Text Full Text PDF PubMed Scopus (125) Google Scholar). Furthermore, protein kinase C-dependent phosphorylation of Ser225 increases the membrane affinity of hSK1. If a phosphorylation-dependent mechanism accounts for IGF-2/M6P receptor-mediated SK1 activation, the identity of the kinase and its mechanism of action remain to be determined. Another finding of our study is that maximum IGF-2-stimulated ERK1/2 activation is about 30% lower than the maximum IGF-1 response, despite the observation that at high concentrations, IGF-1 and IGF-2 promote equivalent phosphorylation of IGF-1 receptor β-subunit Tyr1158. This difference in efficacy may reflect differences in the pattern of receptor or adapter protein phosphorylation generated by two ligands binding to the same receptor. Analogous results have been reported for the epidermal growth factor (EGF) receptor, ErbB1, where binding of EGF and betacellulin generate similar levels of ErbB1 Y1086 phosphorylation, but betacellulin produces greater Akt activation and a more robust anti-apoptotic response than EGF (47Saito T. Okada S. Ohshima K. Yamada E. Sato M. Uehara Y. Shimizu H. Pessin J.E. Mori M. Endocrinology. 2004; 145: 4232-4243Crossref PubMed Scopus (79) Google Scholar, 48Shin H.S. Lee H.J. Nishida M. Lee M.-S. Tamura R. Yamashita S. Matsuzawa Y. Lee I.-K. Koh G.Y. Circ. Res. 2003; 93: 302-310Crossref PubMed Scopus (63) Google Scholar). Alternatively, the reduced IGF-2 response could result from downstream effects on the ERK1/2 pathway due to concomitant IGF-2 receptor activation by IGF-2 but not IGF-1. Given the complexity of the system and the limitations of our current understanding of IGF-2 receptor signaling, the basis of these differences will have to be addressed in future studies. In purified reconstituted systems, only seven membrane-spanning GPCRs have been shown to possess intrinsic ligand-activated guanine nucleotide exchange factor activity for heterotrimeric G proteins. Nonetheless, it is clear that heterotrimeric G proteins mediate a subset of signals initiated by diverse non-heptahelical receptors, including the insulin, IGF-1, EGF, and platelet-derived growth factor receptor tyrosine kinases and single membrane-spanning receptors for C-type natriuretic peptide and zona pellucida glycoprotein, integrins, and T cell receptors (49Patel T.B. Pharm. Rev. 2004; 56: 371-385Crossref PubMed Scopus (86) Google Scholar). Apart from our results with the IGF-1 and IGF-2/M6P receptors (31El-Shewy H.M. Johnson K.R. Lee M.-H. Jaffa A.A. Obeid L.M. Luttrell L.M. J. Biol. Chem. 2006; 281: 31399-31407Abstract Full Text Full Text PDF PubMed Scopus (71) Google Scholar), heterotrimeric G protein activation resulting from SK1-dependent transactivation of S1P receptors has been shown to account for pertussis toxin-sensitive signaling by platelet-derived growth factor receptor (50Hobson J.P. Rosenfeldt H.M. Barak L.S. Olivera A. Poulton S. Caron M.G. Milstien S. Spiegel S. Science. 2001; 291: 1800-1803Crossref PubMed Scopus (384) Google Scholar, 51Waters C. Sambi B. Kong K.-C. Thompson D. Pitson S.M. Pyne S. Pyne N.J. J. Biol. Chem. 2003; 278: 6282-6290Abstract Full Text Full Text PDF PubMed Scopus (123) Google Scholar). Based on this small but growing body of evidence, it is tempting to speculate that S1P receptor transactivation represents a common mechanism of signal convergence that permits structurally diverse non-GPCRs to access heterotrimeric G protein signaling pathways.

Referência(s)