RESUMEN
BACKGROUND: The dogma in psoriasis is that due to pathogen-induced inflammatory responses, an autoreactive immune response is induced that leads to tissue destruction. However, this model might be too simplistic. Literature data suggest that the expression of enzymes crucial for fatty acid oxidation is upregulated in the skin of patients with psoriasis compared with healthy individuals. OBJECTIVES: To examine the influence of fatty acid oxidation on psoriasis with regard to expression and activity of the key enzyme in fatty acid oxidation, carnitine palmitoyltransferase-1 (CPT-1) and the effect of the CPT-1 inhibitor, Etomoxir. METHODS: Experiments were performed with homogenates of lesional and healthy skin, fibroblast cultures and a model of human psoriatic skin transplanted on immune-deficient BNX mice. RESULTS: CPT-1 was highly active in lesional skin. Etomoxir was able to block CPT-1 activity in skin, implying that this antagonist may have the potential to suppress psoriasis when administered topically. In the mouse model, Etomoxir had an antipsoriatic effect that was at least as good as that of betamethasone, as evidenced by reduction of epidermal thickness, keratinocyte proliferation and differentiation. CONCLUSIONS: We conclude that fatty acid metabolism and in particular CPT-1 may be an excellent target for treatment of psoriasis.
Asunto(s)
Compuestos Epoxi/uso terapéutico , Ácidos Grasos/metabolismo , Psoriasis/tratamiento farmacológico , Animales , Carnitina O-Palmitoiltransferasa/antagonistas & inhibidores , Carnitina O-Palmitoiltransferasa/metabolismo , Diferenciación Celular/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Células Cultivadas , Modelos Animales de Enfermedad , Relación Dosis-Respuesta a Droga , Inhibidores Enzimáticos/uso terapéutico , Compuestos Epoxi/farmacocinética , Fibroblastos/metabolismo , Fibroblastos/patología , Humanos , Ratones , Ratones Pelados , Oxidación-Reducción/efectos de los fármacos , Psoriasis/metabolismo , Psoriasis/patología , Piel/enzimología , Trasplante de Piel , Trasplante HeterólogoRESUMEN
Epidemiological studies have revealed a relationship between early growth restriction and the subsequent development of type 2 diabetes. A rat model of maternal protein restriction has been used to investigate the mechanistic basis of this relationship. This model causes insulin resistance and diabetes in adult male offspring. The aim of the present study was to determine the effect of early growth restriction on muscle insulin action in late adult life. Rats were fed either a 20% or an isocaloric 8% protein diet during pregnancy and lactation. Offspring were weaned onto a 20% protein diet and studied at 15 Months of age. Soleus muscle from growth restricted offspring (LP) (of dams fed 8% protein diet) had similar basal glucose uptakes compared with the control group (mothers fed 20% protein diet). Insulin stimulated glucose uptake into control muscle but had no effect on LP muscle. This impaired insulin action was not related to changes in expression of either the insulin receptor or glucose transporter 4 (GLUT 4). However, LP muscle expressed significantly less (P<0.001) of the zeta isoform of protein kinase C (PKC zeta) compared with controls. This PKC isoform has been shown to be positively involved in GLUT 4-mediated glucose transport. Expression levels of other isoforms (betaI, betaII, epsilon, theta) of PKC were similar in both groups. These results suggest that maternal protein restriction leads to muscle insulin resistance. Reduced expression of PKC zeta may contribute to the mechanistic basis of this resistance.
Asunto(s)
Retardo del Crecimiento Fetal/metabolismo , Glucosa/metabolismo , Trastornos del Crecimiento/metabolismo , Insulina/farmacología , Proteínas Musculares , Músculo Esquelético/metabolismo , Animales , Dieta con Restricción de Proteínas , Regulación hacia Abajo , Femenino , Transportador de Glucosa de Tipo 4 , Técnicas In Vitro , Resistencia a la Insulina , Masculino , Modelos Animales , Proteínas de Transporte de Monosacáridos/metabolismo , Embarazo , Proteína Quinasa C/metabolismo , Ratas , Ratas Wistar , Receptor de Insulina/metabolismoRESUMEN
Epidemiological studies have established a relationship between early growth restriction and subsequent development of type 2 diabetes. Animal studies have shown that offspring of protein-restricted rats undergo a greater age-related loss of glucose tolerance than controls. The aim of this study was to investigate the possibility that this deterioration of glucose tolerance is associated with changes in adipocyte insulin action. Adipocytes from low-protein offspring had higher basal levels of glucose uptake than controls. Insulin stimulated glucose uptake into control adipocytes but had little effect on low-protein adipocytes. Both groups had similar levels of basal and isoproterenol-stimulated lipolysis. Insulin inhibited lipolysis in control adipocytes but had a reduced effect on low-protein adipocytes. These changes in insulin action were not related to altered expression of insulin receptors or insulin receptor tyrosine phosphorylation; however, they were associated with reduced phosphatidylinositol 3-kinase and protein kinase B activation. These results demonstrate that reduced glucose tolerance observed in late adult life after early growth restriction is associated with adipocyte insulin resistance.
Asunto(s)
Adipocitos/enzimología , Retardo del Crecimiento Fetal/enzimología , Proteínas Musculares , Fosfatidilinositol 3-Quinasas/metabolismo , Complicaciones del Embarazo , Efectos Tardíos de la Exposición Prenatal , Deficiencia de Proteína/enzimología , Tejido Adiposo/efectos de los fármacos , Tejido Adiposo/metabolismo , Animales , Peso Corporal , Activación Enzimática , Femenino , Glucosa/metabolismo , Transportador de Glucosa de Tipo 4 , Insulina/farmacología , Lipólisis , Masculino , Proteínas de Transporte de Monosacáridos/análisis , Fosfotirosina/metabolismo , Embarazo , Ratas , Ratas Wistar , Receptor de Insulina/análisisRESUMEN
Growth factor induced activation of phosphoinositide 3-kinase and protein kinase B (PKB) leads to increased activity of the mammalian target of rapamycin (mTOR). This subsequently leads to increased phosphorylation of eIF4E binding protein-1 (4EBP1) and activation of p70 ribosomal S6 protein kinase (p70(S6K)), both of which are important steps in the stimulation of protein translation. The stimulation of translation is attenuated in cells deprived of amino acids and this is associated with the attenuation of 4EBP1 phosphorylation and p70(S6K) activation. It has been suggested that PKB regulates mTOR function by phosphorylation although direct phosphorylation of mTOR by PKB has not been demonstrated previously. In the present work, we have found that PKB directly phosphorylates mTOR and, using phosphospecific antibodies, we have shown this phosphorylation occurs at Ser(2448). Insulin also induces phosphorylation on Ser(2448) and this effect is blocked by wortmannin but not rapamycin, consistent with the effect being mediated by PKB. Amino-acid starvation rapidly attenuated the reactivity of the Ser(2448) phosphospecific antibody with mTOR and this could not be restored by either insulin stimulation of cells or incubation with PKB in vitro. Our findings demonstrate that mTOR is a direct target for PKB and support the conclusion that regulation of phosphorylation of Ser(2448) is a point of convergence for the counteracting regulatory effects of growth factors and amino acid levels.
Asunto(s)
Aminoácidos/deficiencia , Insulina/farmacología , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Biosíntesis de Proteínas , Proteínas Quinasas , Proteínas Serina-Treonina Quinasas , Proteínas Proto-Oncogénicas/metabolismo , Androstadienos/farmacología , Inhibidores de las Quinasa Fosfoinosítidos-3 , Fosforilación , Proteínas Proto-Oncogénicas c-akt , Transducción de Señal , Sirolimus/farmacología , Serina-Treonina Quinasas TOR , WortmaninaRESUMEN
The insulin receptor (IR) and type 1 insulin-like growth factor (IGF-I) receptor (IGFR) are both widely expressed in mammalian tissues, and are known to be capable of heteromeric assembly as insulin/IGF hybrid receptors, in addition to the classically described receptors. By selective immunoadsorption of radioligand/receptor complexes and by immunoblotting we have determined the fraction of insulin receptors and IGF receptors occurring as hybrids in different tissues. Microsomal membranes were isolated from tissue homogenates and solubilized with Triton X-100. Solubilized receptors were incubated with 125I-IGF-I, and radioligand/receptor complexes bound by IR-specific and IGFR-specific monoclonal antibodies were quantified. The fraction of IGF-I binding sites behaving as hybrids (anti-IR-bound/anti-IGFR-bound) was approx. 40% in liver and spleen, 70% in placenta, and 85-90% in skeletal muscle and heart, similar results being obtained in rabbit and human tissues. There was no correlation between the proportion of hybrids and the ratio of 125I-insulin/125I-IGF-I binding in different tissues. The fraction of 125I-insulin bound to hybrids was too low for accurate quantification, because of the relatively low affinity of hybrids for insulin. The fraction of insulin receptors present in hybrids was therefore determined by immunoblotting. Receptors in solubilized human placental microsomal membranes were precipitated with IR-specific or IGFR-specific monoclonal antibodies, and after SDS/PAGE, blots were prepared and probed with IR-specific and IGFR-specific antisera. It was found that 15% of IR and 80% of IGFR were present in hybrids. Consistent with these figures, the overall level of IR was estimated, by blotting with the respective antibodies at concentrations shown to give equal signals with equal amounts of receptor, to be 4-fold greater than IGFR. Overall it was concluded that a significant fraction of both IR and IGFR occurs as hybrids in most mammalian tissues, including those that are recognized targets of insulin and IGF action. The fraction of hybrids in different tissues was not a simple function of the relative levels of IR and IGFR, possibly because of heterogeneity of receptor expression in different cell types. However, in placenta the proportions of IR, IGFR and hybrids were consistent with a process of random assembly reflecting the molar ratio of IR and IGFR half-receptors.
Asunto(s)
Receptor de Insulina/análisis , Receptores de Somatomedina/análisis , Animales , Anticuerpos Monoclonales/inmunología , Western Blotting , Membrana Celular/química , Humanos , Immunoblotting , Hígado/química , Músculo Esquelético/química , Placenta/química , Pruebas de Precipitina , Unión Proteica , Multimerización de Proteína , Conejos , Ensayo de Unión Radioligante , Receptor de Insulina/inmunología , Receptores de Somatomedina/inmunología , Bazo/químicaRESUMEN
In summary, it is still unclear which type of PI 3-kinase is involved in the activation of glycogen synthase. However, there is a strong body of evidence to suggest class-1 PI 3-kinase activity is necessary for insulin stimulation of glucose transport and a growing body of evidence to suggest that insulin stimulation of this class of PI 3-kinase is sufficient to stimulate glucose transport. However, the mechanism by which PI 3-kinase lipid products stimulate glucose transport is still not clear.
Asunto(s)
Glucosa/metabolismo , Glucógeno Sintasa/metabolismo , Insulina/farmacología , Insulina/fisiología , Fosfatidilinositol 3-Quinasas/metabolismo , Animales , Transporte Biológico , Activación Enzimática , Fosfatidilinositol 3-Quinasas/clasificaciónRESUMEN
The role of phosphoinositide 3-kinase (PI 3-kinase) in insulin signaling was evaluated in human skeletal muscle. Insulin stimulated both antiphosphotyrosine-precipitable PI 3-kinase activity and 3-O-methylglucose transport in isolated skeletal muscle (both approximately 2-3-fold). Insulin stimulation of 3-O-methylglucose transport was inhibited by the PI 3-kinase inhibitor LY294002 (IC50 = 2.5 microM). The PI 3-kinase adapter subunits were purified from muscle lysates using phosphopeptide beads based on the Tyr-751 region of the platelet-derived growth factor receptor. Immunoblotting of the material adsorbed onto the phosphopeptide beads revealed the presence of p85alpha, p85beta, p55(PIK)/p55gamma, and p50 adapter subunit isoforms. In addition, p85alpha-NSH2 antibodies recognized four adapter subunit variants of 54, 53, 48, and 46 kDa, the latter corresponding to the p50 splice variant. Serial immunoprecipitations demonstrated that these four proteins were associated with a large proportion of the total PI 3-kinase activity immunoprecipitated by p85alpha-NSH2 domain antibodies. Antibodies to p85beta, p55(PIK)/p55gamma, and the p50 adapter subunit also immunoprecipitated PI 3-kinase activity from human muscle lysates. A large proportion of the total cellular pool of the 53-kDa variant, p50, and p55(PIK) was present in antiphosphotyrosine immunoprecipitates from unstimulated muscle, whereas these immunoprecipitates contained only a very small proportion of the cellular pool of p85alpha, p85beta, and the 48-kDa variant. Insulin greatly increased the levels of the 48-kDa variant in antiphosphotyrosine immunoprecipitates and caused smaller -fold increases in the levels of p85alpha, p85beta, and the 53-kDa variant. The levels of p50 and p55(PIK) were not significantly changed. These properties indicate mechanisms by which specificity is achieved in the PI 3-kinase signaling system.
Asunto(s)
Insulina/metabolismo , Músculo Esquelético/metabolismo , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , 3-O-Metilglucosa/metabolismo , Adulto , Cromonas/farmacología , Activación Enzimática , Inhibidores Enzimáticos/farmacología , Humanos , Técnicas In Vitro , Masculino , Peso Molecular , Morfolinas/farmacología , Fosfatidilinositol 3-Quinasas , Fosfopéptidos/metabolismo , Conformación Proteica , Transducción de Señal , Dominios Homologos srcRESUMEN
Insulin action on adipocytes was studied in the offspring of mothers who had been fed either a control (20% protein) or a low (8%)-protein diet during pregnancy and lactation. Adipocytes isolated from low-protein offspring had significantly higher basal and insulin-stimulated glucose uptakes than controls. This may be related to a threefold increase in insulin receptors in low-protein adipocytes. Consistent with these observed changes in glucose transport, adipocytes from low-protein animals had significantly higher basal and insulin-stimulated insulin receptor substrate (IRS)-1-associated phosphatidylinositol 3-kinase (PI 3-kinase) activities. There was also more p85-associated PI 3-kinase activity in these adipocytes. There was no difference in expression in the p85 regulatory subunit or the p110-alpha catalytic subunit of PI 3-kinase. In contrast, there was a sixfold reduction in the p110-beta catalytic subunit of PI 3-kinase in adipocytes from low-protein animals. These results suggest that poor fetal nutrition during pregnancy and lactation can have long-term effects on glucose transport and on the expression of key components of the insulin signaling pathway in adipocytes.
Asunto(s)
Adipocitos/metabolismo , Glucosa/metabolismo , Insulina/farmacología , Complicaciones del Embarazo/fisiopatología , Efectos Tardíos de la Exposición Prenatal , Desnutrición Proteico-Calórica/fisiopatología , Transducción de Señal/fisiología , Adipocitos/efectos de los fármacos , Tejido Adiposo/citología , Tejido Adiposo/metabolismo , Tejido Adiposo/patología , Animales , Peso Corporal , Células Cultivadas , Epidídimo , Femenino , Proteínas Sustrato del Receptor de Insulina , Lactancia , Masculino , Proteínas de Transporte de Monosacáridos/metabolismo , Tamaño de los Órganos , Fosfatidilinositol 3-Quinasas , Fosfoproteínas/metabolismo , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Embarazo , Ratas , Ratas Wistar , Transducción de Señal/efectos de los fármacosRESUMEN
The role of the mammalian target of rapamycin (mTOR) was investigated in insulin responsive cell lines. mTOR was expressed at high levels in insulin responsive cell types and in 3T3-L1 cells mTOR expression levels increased dramatically as cells differentiated from fibroblasts into insulin responsive adipocytes. mTOR localized to membrane fractions in all cells tested and in 3T3-L1 adipocytes mTOR was specifically localized to microsomal membranes. Protein kinase activity directed towards mTOR was tightly associated with mTOR immunoprecipitates and this kinase activity was inhibited by FKBP12-rapamycin indicating it was due to an autokinase activity present in mTOR. The mTOR autokinase and the protein kinase activity of the p110 alpha isoform of PI 3-kinase shared several notable similarities; (a) both were maximally active in the presence of Mn2+ but also showed significant activity in the presence of Mg2+ (b) neither were inhibited by the presence of non-ionic detergent and (c) both were inhibited by wortmannin and LY294002, known inhibitors of the PI 3-kinase lipid kinase activity. These data taken together indicate the autokinase activity lay in the PI 3-kinase homology domain. In summary mTOR is a membrane anchored protein kinase that is active in conditions encountered in vivo and the fact it is highly expressed in insulin responsive cell types is consistent with a role in insulin signalling.
Asunto(s)
Insulina/fisiología , Fosfotransferasas (Aceptor de Grupo Alcohol)/biosíntesis , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Polienos/farmacología , Células 3T3 , Animales , Células CHO , Membrana Celular/enzimología , Cricetinae , Activación Enzimática/efectos de los fármacos , Humanos , Ratones , Proteínas Quinasas/metabolismo , Transducción de Señal/efectos de los fármacos , Sirolimus , Fracciones Subcelulares/enzimología , Serina-Treonina Quinasas TORRESUMEN
Isolated skeletal muscle from healthy individuals was used to evaluate the role of phosphoinositide 3-kinase (PI 3-kinase) in insulin signalling pathways regulating mitogen activated protein kinase (MAP-kinase) and protein kinase-B and to investigate whether MAP-kinase was involved in signalling pathways regulating glucose metabolism. Insulin stimulated glycogen synthase activity (approximately 1.7 fold), increased 3-o-methylglucose transport into human skeletal muscle strips (approximately 2 fold) and stimulated phosphorylation of the p42 ERK-2 isoform of MAP-kinase. This phosphorylation of p42 ERK2 was not blocked by the PI 3-kinase inhibitors LY294002 and wortmannin although it was blocked by the MAP-kinase kinase (MEK) inhibitor PD 98059. However, PD98059 (up to 20 micromol/l) did not block insulin activation of glycogen synthase or stimulation of 3-o-methylglucose transport. Wortmannin and LY294002 did block insulin stimulation of protein kinase-B (PKB) phosphorylation and stimulation of 3-o-methylglucose transport was inhibited by wortmannin (IC50 approximately 100 nmol/l). These results indicate that MAP-kinase is activated by insulin in human skeletal muscle by a PI 3-kinase independent pathway. Furthermore this activation is not necessary for insulin stimulation of glucose transport or activation of glycogen synthase in this tissue.
Asunto(s)
3-O-Metilglucosa/metabolismo , Inhibidores Enzimáticos/farmacología , Glucógeno Sintasa/metabolismo , Insulina/farmacología , Proteína Quinasa 1 Activada por Mitógenos/metabolismo , Músculo Esquelético/enzimología , Fosfatidilinositol 3-Quinasas/metabolismo , Proteínas Serina-Treonina Quinasas , Proteínas Proto-Oncogénicas/metabolismo , 3-O-Metilglucosa/antagonistas & inhibidores , Adulto , Androstadienos/farmacología , Cromonas/farmacología , Relación Dosis-Respuesta a Droga , Flavonoides/farmacología , Glucógeno Sintasa/antagonistas & inhibidores , Humanos , Masculino , Proteína Quinasa 1 Activada por Mitógenos/análisis , Proteína Quinasa 1 Activada por Mitógenos/antagonistas & inhibidores , Morfolinas/farmacología , Músculo Esquelético/efectos de los fármacos , Músculo Esquelético/metabolismo , Músculo Esquelético/patología , Inhibidores de las Quinasa Fosfoinosítidos-3 , Fosforilación , Proteínas Proto-Oncogénicas/antagonistas & inhibidores , Proteínas Proto-Oncogénicas c-akt , WortmaninaRESUMEN
To understand how the stimulation of phosphoinositide 3-kinase (PI 3-kinase) by different growth factors can activate different subsets of downstream responses, growth-factor regulation of PI 3-kinase activity at different intracellular locations was investigated in 3T3-L1 adipocytes. Insulin caused a large stimulation of glucose transport and stimulated recruitment of transferrin receptors to the plasma membrane (PM) in these cells, whereas platelet-derived growth factor (PDGF)-bb was virtually without effect on these responses. Subcellular fractionation studies after stimulation with PDGF-bb or insulin revealed a differential effect of these growth factors on subcellular localization of PI 3-kinase activity. PDGF was more effective than insulin in stimulating PI 3-kinase activity and recruiting the p85 alpha PI 3-kinase adaptor subunit in the fraction containing the PM. However, in the microsomal fraction insulin significantly increased PI 3-kinase activity and p85 alpha levels, whereas PDGF was almost without effect. In the microsomal membrane fraction the insulin-stimulated recruitment of p85 alpha closely matched the increase PI 3-kinase activity, indicating that insulin stimulation of PI 3-kinase in this fraction is largely due to recruitment of PI 3-kinase enzyme rather than alterations in specific activity. Insulin-stimulated recruitment of p85 alpha to the microsomal membranes was not inhibited by wortmannin, indicating that PI 3-kinase activity was not required for this process. A further level of compartment-specific regulation of PI 3-kinase in response to PDGF was revealed by the finding that tyrosine phosphorylation of the p85 alpha adaptor was restricted to the PM-containing fraction. Insulin had no effect on p85 tyrosine phosphorylation in either fraction. In summary, these results suggest a basis by which insulin and PDGF could both use PI 3-kinase signalling cascades but achieve different signalling outcomes.
Asunto(s)
Adipocitos/enzimología , Insulina/farmacología , Proteínas Musculares , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Factor de Crecimiento Derivado de Plaquetas/farmacología , Células 3T3 , Adipocitos/efectos de los fármacos , Androstadienos/farmacología , Animales , Western Blotting , Membrana Celular/enzimología , Desoxiglucosa/metabolismo , Glucosa/metabolismo , Transportador de Glucosa de Tipo 4 , Antagonistas de Insulina/farmacología , Ratones , Proteínas de Transporte de Monosacáridos/metabolismo , Fosfatidilinositol 3-Quinasas , Fosforilación , Fosfotransferasas (Aceptor de Grupo Alcohol)/química , Fosfotirosina/metabolismo , Receptores de Transferrina/metabolismo , Fracciones Subcelulares/enzimología , Wortmanina , Dominios Homologos srcRESUMEN
The effects of insulin and phorbol 12-myristate 13-acetate (PMA) on the levels of cellular phosphoinositides were investigated in 3T3-L1 adipocytes. Stimulation for 4 min with PMA (1 microM) or insulin (10 nM) increased levels of PtdIns(3,4,5)P3 approx. 2-fold and 6-fold respectively. PMA also had a small effect on the cellular levels of PtdIns4P, whereas insulin had no effect on PtdIns4P levels; levels of PtdIns(4,5)P2 and PtdIns3P were not significantly affected by either agent. Insulin increased the levels of the p85 alpha subunit of phosphoinositide (PI) 3-kinase associated with membranes, whereas PMA decreased levels of membrane-associated p85 alpha. PMA did not increase PI 3-kinase activity in anti-phosphotyrosine or anti-p85 immunoprecipitates. The stimulation of glucose transport by insulin or PMA was blocked by 100 nM wortmannin or 10 ng/ml LY294002, indicating that PI 3-kinase is essential for stimulation by both agents. In summary, these results demonstrate: (1) that PMA and insulin stimulate PtdIns(3,4,5)P3 production by distinct mechanisms in 3T3-L1 adipocytes, and (2) that stimulation of PtdIns(3,4,5)P3 production by PMA is likely to be important in signalling pathways leading from PMA stimulation to end-point responses such as glucose transport.
Asunto(s)
Adipocitos/metabolismo , Glucosa/metabolismo , Fosfatos de Fosfatidilinositol/biosíntesis , Acetato de Tetradecanoilforbol/farmacología , Células 3T3 , Adipocitos/efectos de los fármacos , Androstadienos/farmacología , Animales , Transporte Biológico , Western Blotting , Cromonas/farmacología , Inhibidores Enzimáticos/farmacología , Insulina/farmacología , Antagonistas de Insulina/farmacología , Ratones , Morfolinas/farmacología , Fosfatidilinositol 3-Quinasas , Fosfatidilinositoles/metabolismo , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Fosfotirosina/inmunología , Pruebas de Precipitina , WortmaninaAsunto(s)
Adipocitos/citología , Adipocitos/enzimología , Insulina/farmacología , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Células 3T3 , Adipocitos/efectos de los fármacos , Androstadienos/farmacología , Animales , Proteínas Quinasas Dependientes de Calcio-Calmodulina/metabolismo , División Celular/efectos de los fármacos , Expresión Génica/efectos de los fármacos , Genes fos/efectos de los fármacos , Antagonistas de Insulina/farmacología , Ratones , Fosfatidilinositol 3-Quinasas , Polienos/farmacología , Proteínas Serina-Treonina Quinasas/antagonistas & inhibidores , Proto-Oncogenes/efectos de los fármacos , ARN Mensajero/biosíntesis , Proteínas Quinasas S6 Ribosómicas , Transducción de Señal , Sirolimus , WortmaninaAsunto(s)
Adipocitos/enzimología , Insulina/farmacología , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Acetato de Tetradecanoilforbol/farmacología , Células 3T3 , Adipocitos/efectos de los fármacos , Adipocitos/metabolismo , Animales , Transporte Biológico/efectos de los fármacos , Medio de Cultivo Libre de Suero , Desoxiglucosa/metabolismo , Activación Enzimática , Cinética , Ratones , Fosfatidilinositol 3-Quinasas , Fosfotransferasas (Aceptor de Grupo Alcohol)/efectos de los fármacos , Proteína Quinasa C/metabolismoAsunto(s)
Adipocitos/metabolismo , Glucosa/metabolismo , Factor I del Crecimiento Similar a la Insulina/farmacología , Insulina/farmacología , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Factor de Crecimiento Derivado de Plaquetas/farmacología , Receptores de Transferrina/metabolismo , Células 3T3 , Adipocitos/citología , Adipocitos/efectos de los fármacos , Animales , Becaplermina , Transporte Biológico/efectos de los fármacos , División Celular/efectos de los fármacos , ADN/biosíntesis , Desoxiglucosa/metabolismo , Ratones , Fosfatidilinositol 3-Quinasas , Proteínas Proto-Oncogénicas c-sis , Proteínas Recombinantes/farmacología , Transferrina/metabolismoAsunto(s)
Adipocitos/enzimología , Glucógeno Sintasa/metabolismo , Insulina/farmacología , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Proteínas Serina-Treonina Quinasas/metabolismo , Células 3T3 , Adipocitos/efectos de los fármacos , Androstadienos/farmacología , Animales , Transporte Biológico/efectos de los fármacos , Activación Enzimática , Glucosa/metabolismo , Antagonistas de Insulina/farmacología , Cinética , Ratones , Fosfatidilinositol 3-Quinasas , Proteínas Quinasas S6 Ribosómicas , Uridina Difosfato Glucosa/metabolismo , WortmaninaRESUMEN
We have investigated the involvement of phosphoinositide (PI) 3-kinase and p70 ribosomal protein-S6 kinase (p70s6k) in mediating insulin stimulation of glycogen synthesis in 3T3-L1 adipocytes using specific inhibitors. Wortmannin inhibited PI 3-kinase activity (IC50 approximately 10 nM), inhibition being complete at 100 nm. Wortmannin (100 nM) completely blocked the ability of insulin to activate glycogen synthase in 3T3-L1 adipocytes and the ability of insulin to stimulate glucose incorporation into glycogen in 3T3-L1 fibroblasts. Rapamycin, which blocks insulin-stimulated activation of p70s6k, decreased insulin activation of glycogen synthase in a dose-dependent manner (IC50 approximately 0.8 ng/ml), with a maximum approx. 75% inhibition of insulin's stimulatory effect. Rapamycin inhibited insulin-stimulated glucose incorporation into glycogen to a similar extent and with similar dose-dependency, while having no effect on insulin-stimulated glucose transport. We conclude that PI 3-kinase and p70s6k are involved in the signalling pathways by which insulin stimulates glycogen synthase in 3T3-L1 adipocytes.
Asunto(s)
Adipocitos/efectos de los fármacos , Adipocitos/enzimología , Androstadienos/farmacología , Inhibidores Enzimáticos/farmacología , Glucógeno Sintasa/efectos de los fármacos , Glucógeno Sintasa/metabolismo , Glucógeno/biosíntesis , Antagonistas de Insulina/farmacología , Insulina/farmacología , Polienos/farmacología , Células 3T3/citología , Células 3T3/efectos de los fármacos , Células 3T3/enzimología , Animales , Activación Enzimática/efectos de los fármacos , Cinética , Ratones , Fosfatidilinositol 3-Quinasas , Fosfotransferasas (Aceptor de Grupo Alcohol)/antagonistas & inhibidores , Fosfotransferasas (Aceptor de Grupo Alcohol)/metabolismo , Proteínas Serina-Treonina Quinasas/antagonistas & inhibidores , Proteínas Serina-Treonina Quinasas/metabolismo , Proteínas Quinasas S6 Ribosómicas , Sirolimus , Estimulación Química , WortmaninaRESUMEN
The insulin receptor and type 1 insulin-like growth factor (IGF) receptor as classically described are each the product of a single gene. Various receptor subtypes have been described, however, with distinct structures or binding properties. Two of these subtypes have been studied, namely hybrid and atypical IGF-I receptors. Hybrid receptors contain alpha beta halves of both the insulin and the IGF receptor. They are identifiable as a high-affinity IGF-I-binding species reacting with both IGF-receptor-specific and insulin-receptor-specific monoclonal antibodies, and account for a substantial fraction of IGF receptor in many mammalian tissues. Hybrid receptors purified from human placenta bind IGF-I with approximately 25-fold higher affinity than insulin, the affinity for insulin being 10-fold less than that of the classical insulin receptor. It is therefore likely that hybrids will respond more readily to IGF-I than to insulin in vivo. Atypical IGF receptors are characterized by an ability to bind insulin as well as IGFs with relatively high affinity, but are immunologically indistinguishable from classical IGF receptor and do not react with insulin receptor-specific antibodies. The structural basis of atypical binding behaviour is unknown, though the effect is mimicked by binding of certain anti-IGF receptor monoclonal antibodies, which dramatically increase the affinity of the IGF receptor for insulin. Specific physiological roles have not been demonstrated for hybrid or atypical receptors, but the available information concerning their distribution and properties suggests that these receptor subtypes may have an important influence on the specificity of action of insulin and IGFs in vivo.