RESUMEN
A decline in forced expiratory volume (FEV1) is a hallmark of obstructive respiratory diseases, an important cause of morbidity among the elderly. While some data exist on biomarkers that are related to FEV1, we sought to do a systematic analysis of causal relations of biomarkers with FEV1. Data from the general population-based AGES-Reykjavik study were used. Proteomic measurements were done using 4,782 DNA aptamers (SOMAmers). Data from 1,648 participants with spirometric data were used to assess the association of SOMAmer measurements with FEV1 using linear regression. Bi-directional Mendelian randomisation (MR) analyses were done to assess causal relations of observationally associated SOMAmers with FEV1, using genotype and SOMAmer data from 5,368 AGES-Reykjavik participants and genetic associations with FEV1 from a publicly available GWAS (n = 400,102). In observational analyses, 473 SOMAmers were associated with FEV1 after multiple testing adjustment. The most significant were R-Spondin 4, Alkaline Phosphatase, Placental Like 2 and Retinoic Acid Receptor Responder 2. Of the 235 SOMAmers with genetic data, eight were associated with FEV1 in MR analyses. Three were directionally consistent with the observational estimate, Thrombospondin 2 (THBS2), Endoplasmic Reticulum Oxidoreductase 1 Beta and Apolipoprotein M. THBS2 was further supported by a colocalization analysis. Analyses in the reverse direction, testing whether changes in SOMAmer levels were caused by changes in FEV1, were performed but no significant associations were found after multiple testing adjustments. In summary, this large scale proteogenomic analyses of FEV1 reveals protein markers of FEV1, as well as several proteins with potential causality to lung function.
RESUMEN
The global amino acid composition of bacteria growing in different media has been studied. The data reveal significant changes in the amino acid composition in the growth rate range between 0.5 and 2.1 doublings per hour at 37 degrees C. The changes are consistent with a progressive simplification of the protein population and mRNA pools as the growth rates increase.
Asunto(s)
Proteínas Bacterianas/biosíntesis , Escherichia coli/crecimiento & desarrollo , Biosíntesis de Proteínas , Aminoácidos/metabolismo , Proteínas Bacterianas/genética , Escherichia coli/genética , Escherichia coli/metabolismo , CinéticaRESUMEN
Leptin, encoded for by the mouse ob gene, regulates feeding behavior and energy metabolism. Its receptor (Ob-R) is encoded by the mouse diabetic (db) gene and is mutated in the db/db mouse so that it lacks the cytoplasmic domain. We show that the full-length leptin receptor (Ob-Rb), which is believed to transmit the leptin signal, is expressed in pancreatic islets of ob/ob and wild-type mice, as well as in hypothalamus, liver, kidney, spleen, and heart. Recombinant leptin inhibited basal insulin release in the perfused pancreas preparation from ob/ob mice but not in that from Zucker fa/fa rats. Leptin (1-100 nmol/l) also produced a dose-dependent inhibition of glucose-stimulated insulin secretion by isolated islets from ob/ob mice. In contrast, leptin at maximum effective concentration (100 nmol/l) did not inhibit glucose-stimulated insulin secretion by islets from db/db mice. These results provide evidence that a functional leptin receptor is present in pancreatic islets and suggest that leptin overproduction, particularly from abdominal adipose tissue, may modify directly both basal and glucose-stimulated insulin secretion.
Asunto(s)
Proteínas Portadoras/genética , Insulina/metabolismo , Islotes Pancreáticos/metabolismo , Receptores de Superficie Celular , Animales , Técnicas de Cultivo , Expresión Génica , Secreción de Insulina , Leptina , Ratones , Ratones Obesos , Proteínas/farmacología , Ratas , Ratas Mutantes , Receptores de Leptina , Proteínas Recombinantes/farmacología , Tasa de Secreción/efectos de los fármacos , Distribución TisularRESUMEN
We have previously shown that in Escherichia coli the accumulation of five leucine and three methionine tRNA species is regulated so that those tRNA species that translate major codons increase while those that translate minor codons decrease as the growth rate increases. Here, we have analyzed the growth-rate-dependence of another 12 tRNA species. We find that the level of three tRNA species cognate to the major glycine, proline and arginine codons, respectively, increase with increasing growth rates. Conversely, four tRNAs that are cognate to minor codons within the same amino acid families decrease with increasing growth rates. In addition, the glutamyl as well as the phenylalanyl isoacceptor species are accumulated in proportion to the content of these two amino acids in the proteins produced at different growth rates. In summary, the patterns of the growth-rate-dependence for the accumulation of these 17 tRNA species support the interpretation that the major codon preference is an arrangement to maximize the growth rates of bacteria in rich media by optimizing the kinetic efficiency of translation. In contrast, we find that three minor tRNA species cognate to two rare arginine codons and one minor glycine codon, respectively, increase with increasing growth rate. Such findings suggest that there are additional constraints on the accumulation of these tRNA species that may be distinct from those required to optimize the kinetic efficiency of translation.
Asunto(s)
Escherichia coli/crecimiento & desarrollo , ARN de Transferencia/metabolismo , Secuencia de Bases , Northern Blotting , Codón , Escherichia coli/genética , Escherichia coli/metabolismo , Cinética , Datos de Secuencia Molecular , Sondas de Oligonucleótidos , Biosíntesis de Proteínas , ARN Bacteriano/genética , ARN Bacteriano/metabolismo , ARN de Transferencia/genéticaRESUMEN
Activation of the hexosamine biosynthesis pathway leads to insulin resistance in muscle and adipose tissue. In these tissues leptin gene expression is increased by glucosamine. In the present study we found that glucosamine rapidly activates the production of leptin and OB-Rb, which encodes the functional leptin receptor, in both primary pancreatic islets and clonal beta-cells. Secretion of leptin from clonal beta-cells into the medium was detected readily. In addition, the level of the transcripts encoding signal transducer and activator of transcription-3 and -5, both implicated in leptin signal transduction in islet beta-cells, was increased by glucosamine, although to a lesser degree than mRNA levels of leptin and OB-Rb. High glucose (16.7 mM) induced leptin biosynthesis in primary pancreatic islet cells, and the addition of 1 mM palmitate caused an additional incremental effect. The hexosamine-mediated induction of the leptin system in clonal beta-cells was associated with increased responsiveness to leptin, as demonstrated by a 2.6 +/- 0.3-fold (P < 0.01) increase in tyrosine phosphorylation of signal transducer and activator of transcription-3. These findings are the first evidence of inducible leptin production in pancreatic islets and suggest that islet cells, like skeletal muscle, demonstrate a linkage between increased nutrient availability and both leptin expression and leptin responsiveness.
Asunto(s)
Proteínas Portadoras/fisiología , Glucosamina/farmacología , Islotes Pancreáticos/fisiología , Leptina/biosíntesis , Receptores de Superficie Celular , Animales , Células Clonales , ARN Mensajero/fisiología , Receptores de Leptina , Transducción de Señal/efectos de los fármacos , Transducción de Señal/fisiologíaRESUMEN
The ob gene product, leptin, causes significant and dose-dependent inhibition of basal and insulin-stimulated glycogen synthesis in isolated soleus muscle from ob/ob mice, and a smaller, non-significant inhibition in muscle from wild-type mice. Leptin had no inhibitory effect on glycogen synthesis in soleus muscle from the diabetic (db/db) mice, which lack the functional leptin receptor. The full-length leptin receptor (Ob-Rb), is expressed in soleus muscle of both ob/ob and wild-type mice, however with no detectable differences in expression level. These results suggest that hyperleptinaemia may attenuate insulin action on glucose storage in skeletal muscle.
Asunto(s)
Glucógeno/biosíntesis , Músculo Esquelético/metabolismo , Obesidad/metabolismo , Proteínas/farmacología , Receptores de Superficie Celular , Animales , Proteínas Portadoras/genética , Proteínas Portadoras/metabolismo , Femenino , Regulación de la Expresión Génica , Glucosa/metabolismo , Glucógeno/metabolismo , Insulina/farmacología , Leptina , Ratones , Ratones Endogámicos DBA , Ratones Mutantes , Ratones Obesos , Reacción en Cadena de la Polimerasa , ARN Mensajero/análisis , ARN Mensajero/genética , Receptores de Leptina , Proteínas Recombinantes/farmacologíaRESUMEN
Leptin concentrations are elevated in the majority of obese individuals raising the possibility that leptin resistance contributes to their obesity. Peripheral leptin administration for 48 h caused a several-fold increase in mRNA encoding the suppressors of cytokine signaling SOCS-3 and CIS in hypothalamus and peripheral tissues. Paradoxically, CIS and SOCS-3 mRNAs are also elevated in the leptin-deficient ob/ob mouse. Forced expression of CIS in insulinoma cells prevented transactivation mediated by leptin. Thus tissues continuously exposed to leptin and/or other factors associated with obesity accumulate excessive amounts of SOCS-3 and CIS which could provide a potential mechanism for leptin resistance.
Asunto(s)
Hipotálamo/efectos de los fármacos , Proteínas/metabolismo , Proteínas/farmacología , Proteínas Represoras , Transducción de Señal/efectos de los fármacos , Factores de Transcripción , Animales , Secuencia de Bases , Línea Celular , Cartilla de ADN , Hipotálamo/metabolismo , Leptina , Ratones , Proteínas/genética , ARN Mensajero/genética , ARN Mensajero/metabolismo , Proteínas Recombinantes/farmacología , Proteína 3 Supresora de la Señalización de Citocinas , Proteínas Supresoras de la Señalización de CitocinasRESUMEN
Interleukin-1beta (IL-1beta) is a potent inflammatory cytokine involved in type 1 diabetes and acts through defined IL-1beta signaling pathways. In the present work we describe induction of DNA binding activity to signal transducer and activator of transcription (STAT) in response to IL-1beta in clonal insulin-secreting cells. Moreover, IL-1beta activates a short isoform of STAT-3 that potently stimulates transcription. Immunoprecipitation studies reveal an interaction between the activated STAT-3 and the IL-1 receptor accessory protein indicating an association between the two signaling pathways. This may be a novel point of transduction cross talk and an additional mechanism utilised by IL-1beta in the pancreatic beta-cell during the process of type 1 diabetes.
Asunto(s)
Proteínas de Unión al ADN/metabolismo , Insulina/metabolismo , Interleucina-1/farmacología , Transactivadores/metabolismo , Secuencia de Bases , Células Clonales , ADN/genética , ADN/metabolismo , Humanos , Secreción de Insulina , Interleucina-1/metabolismo , Proteína Accesoria del Receptor de Interleucina-1 , Islotes Pancreáticos/citología , Islotes Pancreáticos/efectos de los fármacos , Islotes Pancreáticos/fisiología , Unión Proteica , Proteínas/metabolismo , Receptores de Interleucina-1/metabolismo , Factor de Transcripción STAT3 , Transducción de Señal , TransfecciónRESUMEN
Leptin is a cytokine secreted from adipose tissue at a rate commensurate with the size of the body's fat stores. In addition to its anorectic and thermogenic central actions, leptin is known to act on peripheral tissues, including the pancreatic beta-cell where it inhibits insulin secretion and reduces insulin transcript levels. However, the role of leptin signalling through its full-length receptor, OB-Rb, in the beta-cell remains unclear. In the present study, we show that leptin activates a signal transducer and activator of transcription (STAT)3 signalling mechanism in pancreatic islets and in a rat model of the pancreatic beta-cell, RINm5F. Leptin induced DNA binding to a STAT consensus oligonucleotide and resulted in transcriptional activation from STAT reporter constructs in a manner consistent with STAT3 activation. Western blot analysis confirmed activation of STAT3 in RINm5F and isolated rat islets. Conditions that mimic increased metabolic activity resulted in attenuation of leptin-mediated STAT DNA binding but had no significant effect on STAT3 tyrosine phosphorylation in RINm5F cells. In addition, leptin activated the mitogen activated protein (MAP) kinase pathway in RINm5F cells. The present study provides a framework for OB-Rb signalling mechanisms in the programming of the beta-cell by leptin and suggests that increased metabolic activity may modulate this function.
Asunto(s)
Insulina/metabolismo , Islotes Pancreáticos/metabolismo , Proteínas/metabolismo , Animales , Secuencia de Bases , Sitios de Unión/genética , Calcio/metabolismo , Células Clonales , AMP Cíclico/metabolismo , ADN/genética , ADN/metabolismo , Proteínas de Unión al ADN/genética , Proteínas de Unión al ADN/metabolismo , Diabetes Mellitus Tipo 2/etiología , Diabetes Mellitus Tipo 2/fisiopatología , Humanos , Técnicas In Vitro , Secreción de Insulina , Islotes Pancreáticos/citología , Leptina , Masculino , Obesidad/complicaciones , Obesidad/fisiopatología , Ratas , Ratas Wistar , Factor de Transcripción STAT3 , Transducción de Señal , Transactivadores/genética , Transactivadores/metabolismo , Activación TranscripcionalRESUMEN
Agonists for the retinoid X receptor (RXR), the rexinoids, and the peroxisome proliferator-activated receptor gamma (PPARgamma), the thiazolidinediones, are effective in the treatment of insulin resistance in rodent models by enhancing insulin action and improving glycemic control. In the present study, we compared the effects of rexinoids and a thiazolidinedione on body weight and mitochondrial uncoupling protein (UCP) isoform mRNA expression in the obese Zucker fa/fa rat. Long-term (2 weeks) oral treatment with the rexinoids LG100268 and LG100324 reduced food intake and body weight gain, whereas rosiglitazone (BRL49653) tended to increase both food intake and weight gain. LG100268 and LG100324 increased brown adipose tissue (BAT) UCP-1 mRNA content by 2.7-fold (P < .002) and 3.1-fold (P < .001), respectively, while BRL49653 had no effect on BAT UCP-1 mRNA content. Neither the rexinoids nor the thiazolidinedione had any effect on the level of mRNA encoding UCP-2 and the recently described PPARgamma coactivator-1 (PGC-1). LG100324 increased UCP-3 mRNA content by 3.6-fold (P < .0005) in muscle and 4.3-fold (P < .0002) in white adipose tissue (WAT). LG100268 increased UCP-3 mRNA content in WAT by 2-fold (P < .005) but was without any effect on muscle UCP-3. BRL49653 increased UCP-3 mRNA content by 2.1-fold (P < .005) in muscle and 2.7-fold (P < .003) in WAT. Thus, the rexinoids, but not the thiazolidinedione, have an antiobesity action by reducing food intake, and the increase in UCP-1 mRNA content in BAT may reflect a stimulation of BAT UCP-1 activity.
Asunto(s)
Peso Corporal/efectos de los fármacos , Proteínas Portadoras/metabolismo , Proteínas de la Membrana/metabolismo , Proteínas de Transporte de Membrana , Proteínas Mitocondriales , Obesidad/metabolismo , Obesidad/patología , Receptores de Ácido Retinoico/agonistas , Tiazoles/farmacología , Tiazolidinedionas , Factores de Transcripción/agonistas , Tejido Adiposo Pardo/metabolismo , Animales , Proteínas Portadoras/genética , Ingestión de Alimentos/efectos de los fármacos , Canales Iónicos , Proteínas de la Membrana/genética , Ácidos Nicotínicos/farmacología , Proteínas/genética , Proteínas/metabolismo , ARN Mensajero/metabolismo , Ratas , Ratas Zucker/anatomía & histología , Ratas Zucker/metabolismo , Receptores X Retinoide , Rosiglitazona , Tetrahidronaftalenos/farmacología , Proteína Desacopladora 1 , Proteína Desacopladora 2 , Proteína Desacopladora 3 , Aumento de Peso/efectos de los fármacosRESUMEN
We have studied the involvement of the factor for inversion stimulation (FIS) in the growth rate-dependent expression of the arginine, leucine, and methionine acceptor tRNA species. The concentration of individual tRNA species relative to 16 S rRNA was determined by blot hybridization using RNA preparations from bacteria with the fis gene deleted and from isogenic wild type bacteria. The RNA preparations were obtained from bacteria growing under steady state conditions in different media. The levels of tRNA(1Leu), tRNA(2Arg), tRNA(4Arg), and tRNA(5Arg decreased in the fis bacteria, relative to the wild type. The difference in levels increased with increasing growth rate. Surprisingly, tRNA(3Leu), tRNA(rMet), and tRNA(eMet) showed the opposite response, with an increase of the tRNA/16 S ratio in the fis bacteria. The tRNA(2Leu, tRNA(4Leu), tRNA(5Leu), and tRNA(3 Arg) had unaffected tRNA/16 S ratios in fis cells. We conclude that FIS, directly or indirectly, is involved in growth rate regulation of some tRNA species and that it affects the composition of the cellular tRNA pool.
Asunto(s)
Proteínas Portadoras/metabolismo , Inversión Cromosómica , Proteínas de Unión al ADN/metabolismo , Proteínas de Escherichia coli , Escherichia coli/genética , Regulación Bacteriana de la Expresión Génica , ARN de Transferencia de Arginina/biosíntesis , ARN de Transferencia de Leucina/biosíntesis , ARN de Transferencia de Metionina/biosíntesis , Secuencia de Bases , Sitios de Unión , Northern Blotting , Proteínas Portadoras/genética , ADN Bacteriano/metabolismo , Escherichia coli/crecimiento & desarrollo , Escherichia coli/metabolismo , Factor Proteico para Inverción de Estimulación , Genes Bacterianos , Factores de Integración del Huésped , Cinética , Datos de Secuencia Molecular , ARN Bacteriano/biosíntesis , ARN Bacteriano/aislamiento & purificación , ARN Bacteriano/metabolismo , ARN Ribosómico 16S/biosíntesis , ARN Ribosómico 16S/metabolismo , ARN de Transferencia de Arginina/genética , ARN de Transferencia de Leucina/genética , ARN de Transferencia de Metionina/genética , Secuencias Reguladoras de Ácidos NucleicosRESUMEN
We have previously shown that the accumulation of 20 tRNA species in Escherichia coli is individually regulated as a function of cellular growth rate. We have also reported that the growth rate regulation of some but not all tRNA species is dependent on the activity of the factor for inversion stimulation (FIS). In present work, we studied the growth rate regulation of the serine- and threonine-accepting tRNA families. We show that the levels of tRNA(3Thr), tRNA(3Ser), tRNA(2Thr), tRNA(3Thr), and tRNA(4Thr) are reduced in fis cells as the growth rate increases. The accumulation of these tRNA species is reduced 2-5-fold at the fastest bacterial growth rate. The strongest effect is observed for the two minor tRNA species; tRNA(2Ser) and tRNA(2Thr). In contrast, we find that the accumulation of tRNA(1Ser), tRNA(5Ser), and tRNA(1Thr) is similar in wild type and fis bacteria. The data presented provide further evidence for the suggestion that FIS is a stimulating factor that is involved, directly or indirectly, in the high expression level of some tRNA genes at fast bacterial growth rates.
Asunto(s)
Proteínas Portadoras/fisiología , Proteínas de Escherichia coli , Escherichia coli/crecimiento & desarrollo , ARN de Transferencia de Serina/metabolismo , ARN de Transferencia de Treonina/metabolismo , Secuencia de Bases , Factor Proteico para Inverción de Estimulación , Retroalimentación , Regulación de la Expresión Génica , Factores de Integración del Huésped , Datos de Secuencia Molecular , ARN de Transferencia de Serina/genética , ARN de Transferencia de Treonina/genéticaRESUMEN
We have tested the predictions of a model that accounts for the codon preferences of bacteria in terms of a growth maximization strategy. According to this model the tRNA species cognate to minor and major codons should be regulated differently under different growth conditions: the isoacceptors cognate to major codons should increase at fast growth rates while those cognate to minor codons should decrease at fast growth rates. We have used a quantitative Northern blotting technique to measure the abundance of the methionine and the leucine isoacceptor families over growth rates ranging from 0.5 to 2.1 doublings per hour. Five tRNA species that are cognate to major codons (tRNA(eMet), tRNA(1fMet), tRNA(2fMet), tRNA(1Leu) and tRNA(3Leu) increase both as a relative fraction of total tRNA and in absolute concentration with increasing growth rates. Three tRNA species that are cognate to minor codons (tRNA(2Leu), tRNA(4Leu) and tRNA(5Leu) decrease as a relative fraction of total RNA and in absolute concentration with increasing growth rates. These data suggest that the abundances of groups of tRNA species are regulated in different ways, and that they are not regulated simply according to isoacceptor specificity. In particular, the data support the growth optimization model for codon bias.
Asunto(s)
Escherichia coli/genética , ARN de Transferencia/metabolismo , Ribosomas/metabolismo , Secuencia de Bases , Northern Blotting , Escherichia coli/crecimiento & desarrollo , Datos de Secuencia Molecular , ARN de Transferencia de Leucina/metabolismo , ARN de Transferencia de Metionina/metabolismoRESUMEN
We have used an affinity electrophoresis assay which when combined with Northern hybridization techniques permits us to estimate the degree of thiolation of individual tRNA species in Escherichia coli. We observe that the levels of 4-thio 2'(3')-uridine (4-thioU) in many but not all tRNAs varies dramatically at different bacterial growth rates: Five tRNAs are completely thiolated at all growth rates, while another eight tRNAs are incompletely thiolated and the fraction of the unthiolated form of these tRNA species increases as the growth rates increase. Transfer RNA(2Glu) contains 4-thioU as well as (methylamino)methyl-2-thio uridine (mnm(5)2-thioU). The level of mnm(5)2-thioU of tRNA(2Glu) is invariant with growth rate. Surprisingly, none of the thirteen tRNA species that we have studied is completely unmodified in all growth media. In particular, at the slowest growth rates every tRNA class that we have studied contains a form that has 4-thioU residues.
Asunto(s)
Escherichia coli/crecimiento & desarrollo , ARN Bacteriano/metabolismo , ARN de Transferencia/metabolismo , Tiouridina/metabolismo , Secuencia de Bases , Northern Blotting , Escherichia coli/genética , Cinética , Datos de Secuencia Molecular , Biosíntesis de Proteínas/genética , ARN Bacteriano/genéticaRESUMEN
OBJECTIVE: Previous studies have demonstrated that leptin can stimulate proliferation of insulin-secreting tumor cell lines. The objective of this study was to characterize whether leptin could stimulate proliferation of primary beta-cells too. Since adult beta-cells have very limited capacity for replication, we examined the effect of leptin on islets of Langerhans obtained from fetal rats, in a tissue culture system. METHODS: Leptin receptor mRNA and c-fos mRNA were measured by RT-PCR. Proliferation of fetal rat islet cells was measured by a WST-1 colorimetric assay and [3H]-thymidine incorporation assay. RESULTS: Leptin stimulated proliferation of serum-deprived fetal rat islet cells, as indicated by increased formation of formazan dye from a tetrazolium salt WST-1. Leptin stimulated DNA synthesis in islet cells, as indicated by increased [3H]-thymidine incorporation into DNA. The effect of leptin on islet cell proliferation was on average 39-50% of the effect obtained with 10% fetal bovine serum. Leptin increased c-fos mRNA expression by 2.8-fold in isolated fetal islets after 30 min treatment. In fetal pancreatic islets, both the common extracellular portion (OB-R) and the intact long form (OB-Rb) of the leptin receptor were readily detected by reverse transcriptase polymerase chain reaction. CONCLUSION: Functional leptin receptors are expressed in pancreatic islet cells, as early as during the fetal stage of development of these microorgans. Leptin stimulates proliferation of fetal islet cells and might play a role in determining islet cell mass at birth.
Asunto(s)
Proteínas Portadoras/genética , Islotes Pancreáticos/efectos de los fármacos , Islotes Pancreáticos/embriología , Leptina/farmacología , Leptina/fisiología , Receptores de Superficie Celular , Animales , Proteínas Portadoras/metabolismo , División Celular/efectos de los fármacos , Colorimetría , Técnicas de Cultivo , Femenino , Regulación del Desarrollo de la Expresión Génica , Genes fos/genética , Humanos , Islotes Pancreáticos/fisiología , Reacción en Cadena de la Polimerasa , Embarazo , ARN Mensajero/análisis , Ratas , Ratas Sprague-Dawley , Receptores de Leptina , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Transcripción GenéticaRESUMEN
The mitochondrial uncoupling protein UCP-1 uncouples respiration from ATP synthesis in brown adipose tissue (BAT) and thus energy is dissipated as heat. Recently two further isoforms have been identified which may play a similar role in other tissues. We have determined the effects of the rodent-selective beta3-adrenoceptor (beta3-AR) agonist BRL 35135, on beta3-AR and UCP mRNA levels in tissues from lean and obese (fa/fa) Zucker rats. beta3-AR mRNA levels were reduced in fa/fa white (WAT) and brown (BAT) adipose tissue relative to levels in lean littermates. BRL 35135 treatment increased expression levels of beta3-AR mRNA in both genotypes. UCP-2 and UCP-3 mRNA levels in BAT, WAT and skeletal muscle were reduced by 2-3 fold in the fa/fa rats relative to the lean rats. We confirm that BRL 35135 increases BAT UCP-1 mRNA in lean rats, and find that BAT UCP-3 mRNA was reduced 3.2 fold, with no changes in UCP-2 expression. In WAT BRL 35135 increased UCP-2 and UCP-3 expression 2-3 fold in both lean and fa/fa rats. In lean rats, skeletal muscle UCP-3 mRNA was increased 2.3 fold by BRL 35135 whereas UCP-2 was reduced by 2.2 fold. BRL 35135 had no effects on UCP-2 and UCP-3 expression in skeletal muscle of the fa/fa rats. Our results demonstrate that mechanisms regulating UCP isoform synthesis in fa/fa rats are impaired and that WAT could be involved in the thermogenic response of BRL 35135.
Asunto(s)
Agonistas Adrenérgicos beta/farmacología , Proteínas Portadoras/genética , Proteínas de la Membrana/genética , Proteínas de Transporte de Membrana , Proteínas Mitocondriales , Fenetilaminas/farmacología , ARN Mensajero/genética , Tejido Adiposo/efectos de los fármacos , Tejido Adiposo/metabolismo , Tejido Adiposo Pardo/efectos de los fármacos , Tejido Adiposo Pardo/metabolismo , Animales , Secuencia de Bases , Regulación de la Temperatura Corporal/efectos de los fármacos , Cartilla de ADN/genética , Expresión Génica/efectos de los fármacos , Canales Iónicos , Músculo Esquelético/efectos de los fármacos , Músculo Esquelético/metabolismo , Obesidad/genética , Obesidad/metabolismo , Reacción en Cadena de la Polimerasa , Proteínas/genética , ARN Mensajero/metabolismo , Ratas , Ratas Zucker , Proteína Desacopladora 1 , Proteína Desacopladora 2 , Proteína Desacopladora 3RESUMEN
The adipocyte hormone leptin activates signal transducer and activator of transcription 3 (STAT3) in the hypothalamus, mediating increased satiety and increased energy expenditure. To date, leptin-mediated activation of the STAT pathway in vivo has not been established in tissues other than hypothalamus. We now describe leptin receptor expression and in vivo signaling in discrete regions of the mouse gastrointestinal tract. Expression of the functional isoform leptin receptor (OB-Rb) is restricted to the jejunum and is readily detected by RT-PCR in isolated enterocytes from this site. Intravenous injection of leptin rapidly induced nuclear STAT5 DNA binding activity in jejunum of +/+ and obese (ob/ob) mice but had no effect in the diabetic (db/db) mouse that lacks the OB-Rb isoform. In addition, an induction of the immediate-early gene c-fos is observed in jejunum in vivo. Leptin-mediated induction of a number of immediate-early genes and activation of STAT3 and STAT5 in a human model of small intestine epithelium, CACO-2 cells, corroborate this effect. Furthermore, intravenous leptin administration caused a significant 2-fold reduction in the apolipoprotein AIV transcript levels in jejunum 90 min after a fat load. Our results suggest that the epithelium of jejunum is a direct target of leptin action, and this activity is dependent on the presence of OB-Rb. Lack of leptin or resistance to leptin action in this site may contribute to obesity and its related syndromes by directly affecting lipid handling.
Asunto(s)
Yeyuno/efectos de los fármacos , Proteínas de la Leche , Proteínas/farmacología , Receptores de Superficie Celular , Animales , Apolipoproteínas A/metabolismo , Células CACO-2 , Proteínas Portadoras/metabolismo , Proteínas de Unión al ADN/análisis , Proteínas de Unión al ADN/metabolismo , Grasas de la Dieta , Femenino , Regulación de la Expresión Génica/efectos de los fármacos , Genes fos/genética , Humanos , Inyecciones Intravenosas , Leptina , Metabolismo de los Lípidos , Ratones , Ratones Endogámicos , Ratones Obesos , Obesidad/etiología , ARN Mensajero/efectos de los fármacos , Receptores de Leptina , Factor de Transcripción STAT3 , Factor de Transcripción STAT5 , Transactivadores/metabolismo , Transcripción Genética/efectos de los fármacosRESUMEN
The ob gene product leptin over the concentration range 0.1-100 nM demonstrated a U-shaped dose-response inhibition of glucose-stimulated insulin secretion by rat pancreatic islets. Thus, leptin (1 and 10 nM) produced a significant inhibition whereas 100 nM was ineffective. The inhibitory effect of leptin was glucose dependent, had a rapid onset and was readily reversed upon removal of leptin. Sub-chronic exposure of islets to leptin (10 nM) reduced both insulin secretion and the level of insulin transcript. These findings support the hypothesis that excessive production of leptin by adipose tissue could play a role in the development of non-insulin dependent diabetes in obese subjects.
Asunto(s)
Insulina/genética , Insulina/metabolismo , Islotes Pancreáticos/metabolismo , Proteínas/farmacología , ARN Mensajero/efectos de los fármacos , Receptores de Superficie Celular , Animales , Proteínas Portadoras/biosíntesis , Separación Celular , Relación Dosis-Respuesta a Droga , Secreción de Insulina , Islotes Pancreáticos/efectos de los fármacos , Isomerismo , Leptina , Masculino , Ratones , Datos de Secuencia Molecular , Obesidad/metabolismo , Proteínas/metabolismo , ARN Mensajero/biosíntesis , Ratas , Ratas Wistar , Receptores de LeptinaRESUMEN
In addition to its interaction at hypothalamic sites to affect feeding and energy expenditure, leptin has been shown to exhibit a proliferative response in erythropoietic cells. The functional leptin receptor is also present in pancreatic islets and we now demonstrate that a commonly used clonal insulin secreting beta-cell line, RINm5F, expresses high levels of the Ob-Rb mRNA. Leptin causes an increase in tyrosine phosphorylation of a number of intracellular proteins and a dose related (10 nM-200 nM) increase in expression of the immediate-early gene, c-fos. This precedes a leptin induced proliferative response in serum-deprived RINm5F cells, which suggests that leptin might be involved in the complex regulation of proliferation of the pancreatic beta-cell.