RESUMEN
Novel biomarkers of rheumatoid arthritis (RA), in addition to antibodies against cyclic citrullinated peptides, are required. Metabolome analysis is a promising approach to identify metabolite biomarkers for clinical diagnosis. We adopted a comprehensive non-targeted metabolomics approach combining capillary electrophoresis time-of-flight mass spectrometry (TOFMS) and liquid chromatography TOFMS. We constructed metabolomics profiling of 286 plasma samples of a Japanese population [92 RA patients, 13 systemic lupus erythematosus (SLE) patients and 181 healthy controls). RA case-control association tests showed that seven metabolites exhibited significantly increased levels in RA samples compared with controls (P < 1.0 × 10-4; UTP, ethanolamine phosphate, ATP, GDP, ADP, 6-aminohexanoic acid and taurine), whereas one exhibited a decreased level (xanthine). The plasma levels of these eight metabolites were not significantly different between seropositive and seronegative RA patients (P > 0.05; n = 68 and 24, respectively). The four nucleotide levels (UTP, ATP, GDP and ADP) were significantly higher in the non-treatment patients in comparison between patients with and without treatment (P < 0.014; n = 57 and 35, respectively). Furthermore, we found that none of the four nucleotide levels showed significant differences in SLE case-control association tests (P > 0.2; 13 patients with SLE and the 181 shared controls) and psoriatic arthritis (PsA) case-control association tests (P > 0.11; 42 patients with PsA and 38 healthy controls), indicating disease specificity in RA. In conclusion, our large-scale metabolome analysis demonstrated the increased plasma nucleotide levels in RA patients, which could be used as potential clinical biomarkers of RA, especially for seronegative RA.
Asunto(s)
Adenosina Difosfato/sangre , Adenosina Trifosfato/sangre , Artritis Reumatoide/sangre , Artritis Reumatoide/diagnóstico , Guanosina Difosfato/sangre , Uridina Trifosfato/sangre , Artritis Psoriásica/sangre , Biomarcadores/sangre , Humanos , Japón , Lupus Eritematoso Sistémico/sangre , Metaboloma , MetabolómicaRESUMEN
Recent progress in our understanding of the regulation of the phagocyte NADPH oxidase by the Rac GTP-binding protein(s) has provided the first detailed glimpse into the mechanisms of leukocyte regulation by a small GTP-binding protein. Studies over the past year have indicated that the activity of the NADPH oxidase can be modulated by regulation of the GTP/GDP state of Rac. Proteins exist in leukocytes that are able to modify GTP-binding protein function in this manner, and their activity may be regulated by signals generated upon phagocyte stimulation.
Asunto(s)
Proteínas de Unión al GTP/metabolismo , NADH NADPH Oxidorreductasas/sangre , Neutrófilos/fisiología , Fagocitosis , Animales , Quimiotaxis de Leucocito , Guanosina Difosfato/sangre , Guanosina Trifosfato/sangre , Homeostasis , Humanos , Modelos Biológicos , NADPH Oxidasas , Proteínas de Unión al GTP racRESUMEN
6-Thioguanine nucleotides are the sum of 6-thioguanosine 5'-monophosphate (TGMP), -diphosphate (TGDP), and -triphosphate (TGTP) representing essential metabolites involved in drug action of thiopurines. Elevated levels of TGDP have been associated with poor response to azathioprine therapy in patients with inflammatory bowel disease. The conversion of TGDP to TGTP is supposed to be catalyzed by nucleoside diphosphate kinase (NDPK). The aim of this work was to investigate simultaneously individual 6-thioguanosine phosphate levels and NDPK activity in red blood cells (RBCs) of patients on azathioprine therapy. Ion-pair high-performance liquid chromatography methods with fluorescence and ultraviolet detection were applied to quantify individual levels of 6-thioguanosine 5'-phosphates and NDPK activity, respectively, in RBCs. Recombinantly expressed NDPK isoforms A and B were unequivocally identified to catalyze the formation of TGTP (30.6 +/- 3.88 nmol x min x mg for NDPK A versus 41.2 +/- 1.05 nmol x min x mg for NDPK B). Comprehensive analyses on the stability of TGMP, TGDP, and TGTP and the reproducibility of NDPK activity in RBCs were performed to provide a reliable sampling protocol for clinical practice. Of note, isolation of RBCs within 6 hours followed by immediate storage at -80 degrees C is crucial for prevention of degradation of 5'-phosphates. In a clinical study of 37 patients on azathioprine, TGTP was the predominant 6-thioguanosine phosphate in RBCs. In contrast, three patients showed TGTP/(TGDP + TGTP) ratios of 57.2%, 64.3%, and 66% corresponding to elevated TGDP levels. NDPK activity ranged from 4.1 to 11.3 nmol x min x mg hemoglobin. No correlation between NDPK activity and the 6-thioguanosine phosphate levels was found. The question whether interindividual variability of NDPK activity may explain differences in 6-thioguanosine 5'-phosphates levels has to be investigated in a prospective large-scale study.
Asunto(s)
Azatioprina/administración & dosificación , Sistemas de Liberación de Medicamentos/tendencias , Eritrocitos/efectos de los fármacos , Eritrocitos/enzimología , Guanosina Difosfato/análogos & derivados , Guanosina Trifosfato/análogos & derivados , Nucleósido-Difosfato Quinasa/sangre , Purinas/uso terapéutico , Tionucleótidos/sangre , Adolescente , Adulto , Anciano , Catálisis , Activación Enzimática/efectos de los fármacos , Activación Enzimática/fisiología , Femenino , Guanosina Difosfato/sangre , Guanosina Trifosfato/sangre , Humanos , Masculino , Persona de Mediana Edad , Adulto JovenRESUMEN
5-Amino-4-imidazolecarboxamide riboside 5'-monophosphate (ZMP) is an intermediate in the purine de novo synthetic pathway that may be further metabolized to inosine 5'-monophosphate, degraded to the corresponding nucleoside (5-amino-4-imidazole-carboxamide riboside; Z-riboside), or phosphorylated to the corresponding 5'-triphosphate (ZTP). Accumulation of ZTP in microorganisms has been associated with depletion of folate intermediates that are necessary for the conversion of ZMP to inosine 5'-monophosphate and has been postulated to play a regulatory role in cellular metabolism. We have shown the presence of Z-nucleotides in erythrocytes derived from five individuals with the Lesch-Nyhan syndrome. Erythrocyte folate levels were within the normal range, although guanosine triphosphate levels were significantly reduced below those in normal controls (P less than 0.01). A small amount of Z-nucleotide accumulation was also found in one individual with partial deficiency of the enzyme hypoxanthine guanine phosphoribosyltransferase and in two individuals with other disorders of purine overproduction. In contrast, no Z-nucleotides were detected in 13 normal controls or in three individuals with hyperuricemia on allopurinol therapy. We conclude that Z-nucleotide formation may result from markedly increased rates of de novo purine biosynthesis. It is possible that metabolites of these purine intermediates may play a role in the pathogenesis of the Lesch-Nyhan syndrome.
Asunto(s)
Aminoimidazol Carboxamida/sangre , Eritrocitos/metabolismo , Imidazoles/sangre , Síndrome de Lesch-Nyhan/metabolismo , Ribonucleótidos/sangre , Aminoimidazol Carboxamida/análogos & derivados , Aminoimidazol Carboxamida/metabolismo , Guanosina Difosfato/sangre , Guanosina Trifosfato/sangre , Humanos , Síndrome de Lesch-Nyhan/sangre , Ribonucleótidos/metabolismoRESUMEN
Preincubation of human platelet membranes with the ATP analog ATP[gamma S] led to persistent adenylate cyclase activation. This stimulation was increased by copreincubation with PGE1 and obliterated by removing endogenous GDP by the NTP-regenerating system, creatine phosphate plus creatine kinase. PGE1 partially reversed the action of the regenerating system. Control formation of GTP[gamma S] from ATP[gamma S] and GDP in platelet membranes was apparently not stimulated by PGE1. In contrast, in the presence of creatine phosphate plus creatine kinase, which prevented formation of GTP[gamma S], PGE1 stimulated formation of this GTP analog, by partially reversing the action of the NTP-regenerating system. The data indicate that GTP[gamma S] can be formed by a membrane-associated nucleoside diphosphokinase from ATP[gamma S] and GDP, resulting in persistent Gs-protein activation, and that this process can be stimulated by an agonist-activated receptor.
Asunto(s)
Plaquetas/metabolismo , Proteínas de Unión al GTP/sangre , Guanosina Trifosfato/análogos & derivados , Tionucleótidos/sangre , Adenosina Trifosfato/análogos & derivados , Adenosina Trifosfato/sangre , Adenosina Trifosfato/farmacología , Adenilil Ciclasas/sangre , Alprostadil/farmacología , Membrana Celular/metabolismo , Creatina Quinasa/metabolismo , Activación Enzimática/efectos de los fármacos , Guanosina 5'-O-(3-Tiotrifosfato) , Guanosina Difosfato/sangre , Guanosina Difosfato/farmacología , Guanosina Trifosfato/sangre , Humanos , Magnesio/farmacología , Cloruro de Magnesio , Fosfocreatina/metabolismoRESUMEN
Nutritional surveys have demonstrated that Hb levels in blacks are consistently lower than in whites. This difference does not appear to be related to socioeconomic dietary differences, or differences of hereditary disorders such as sickle cell disease. We studied 47 black and 63 white subjects drawn from hospital employees. Mean Hb of black men was 0.9 g/dl less than that of white men. Mean Hb of black women was 0.5 g/dl less than that of white women. This difference was not associated with differences of serum iron, iron binding capacity, or transferrin saturation. Ferritin values of white women were significantly less than values observed in white men, but similar differences were not observed between black men and women. The explanation for this is unclear although may be related to sample size or differences of menstrual status. Copper levels were lower in white men than in any other group, and zinc levels were essentially similar between racial groups. The red blood cells of blacks were also smaller than those of whites. This difference could not be explained by disordered Hb synthesis. These observations confirm that Hb concentrations in both black men and women are lower than in their white counterparts. This difference cannot be explained by differences in iron, copper, or zinc nutriture. Further, measurements of Hb in nutritional survey populations reflect iron status as only one of several variables and should not be used as the only assessment of iron nutrition.
Asunto(s)
Población Negra , Cobre/sangre , Hemoglobinas/análisis , Hierro/sangre , Población Blanca , Zinc/sangre , Adulto , Ceruloplasmina/análisis , Índices de Eritrocitos , Femenino , Guanosina Difosfato/sangre , Humanos , Masculino , Persona de Mediana Edad , Transferrina/análisisRESUMEN
Significant gestational changes in red cell 2,3-DPG were found. No significant correlation was found between these pregnancy-related changes and alterations in the parameters of iron metabolism or red cell enzymes during the same gestational period. Possible reasons for the high concentration found at 21--24 weeks gestation are discussed.
Asunto(s)
Ácidos Difosfoglicéricos/sangre , Embarazo , Eritrocitos/enzimología , Femenino , Ferritinas/sangre , Guanosina Difosfato/sangre , Hemoglobinas/metabolismo , Humanos , Periodo Posparto , Segundo Trimestre del Embarazo , Tercer Trimestre del Embarazo , Piruvato Quinasa/sangre , Transferrina/sangreRESUMEN
We report the development and application of a novel assay for high affinity binding of the agonist [3H]hydrozybenzyl-isoproterenol simultaneously with the agonist-promoted release of membrane bound [32P]GDP in the frog erythrocyte beta-adrenergic receptor system. We find that under various assay conditions both events occur with the same rate, ranging from 0.05 to 0.5 min-1. Addition of the non-hydrolyzable guanine nucleotide, guanylyl-imidodiphosphate simultaneously increases the rate of high affinity agonist binding and agonist promoted GDP release. In addition, the guanine nucleotide analog decreases the steady state level of high affinity agonist binding and increases the steady state level of agonist promoted GDP release with comparable potencies of 0.5 microM and 0.1 microM, respectively. The decrement in the steady state level of high affinity agonist binding (180 fmol/mg protein) due to the guanine nucleotide analog is in the same range as the reciprocal increment in the extent of agonist-induced [32P]GDP release (180 fmol/mg protein). The concommittant activation of adenylate cyclase, by submaximal concentrations of the agonist [3H]hydroxybenzylisoproterenol and guanylylimido-diphosphate under similar assay conditions proceeds with the same rate as for the two other measured functions of the system, i.e. 3H-agonist binding and agonist-promoted [32P]GDP release. This represents the first attempt at comparing the time course of adenylate cyclase activation with that of agonist binding and GDP release under similar assay conditions. The results indicate that GDP is not released prior to but rather coincident with formation of the complex of the hormone receptor with the regulatory protein and that enzyme activation proceeds with the same time course as agonist binds to the receptor. It is concluded that both high affinity agonist binding and GDP release represent integral aspects of the rate limiting step in the enzyme activation mechanism.
Asunto(s)
Adenilil Ciclasas/sangre , Membrana Eritrocítica/metabolismo , Eritrocitos/metabolismo , Nucleótidos de Guanina/sangre , Guanosina Difosfato/sangre , Isoproterenol/análogos & derivados , Receptores Adrenérgicos beta/metabolismo , Receptores Adrenérgicos/metabolismo , Animales , Anuros , Relación Dosis-Respuesta a Droga , Activación Enzimática/efectos de los fármacos , Guanilil Imidodifosfato/farmacología , Isoproterenol/metabolismo , Isoproterenol/farmacología , CinéticaRESUMEN
Development of heat stroke led to a decrease in main reactions of energy production and energy potential in erythrocytes, to a decrease in activity of Na+, K+-ATPase and in content of sodium and potassium as well as to alterations in forms and to decrease in volume of these cells.
Asunto(s)
Metabolismo Energético , Eritrocitos/metabolismo , Agotamiento por Calor/metabolismo , Potasio/sangre , ATPasa Intercambiadora de Sodio-Potasio/sangre , Sodio/sangre , Adenosina Trifosfato/sangre , Animales , Eritrocitos/enzimología , Eritrocitos/patología , Femenino , Glucólisis , Guanosina Difosfato/sangre , Agotamiento por Calor/sangre , Agotamiento por Calor/patología , Masculino , RatasAsunto(s)
Adenilil Ciclasas/sangre , Membrana Eritrocítica/metabolismo , Eritrocitos/metabolismo , Nucleótidos de Guanina/sangre , Guanosina Difosfato/sangre , Receptores Adrenérgicos beta/metabolismo , Receptores Adrenérgicos/metabolismo , Animales , Membrana Eritrocítica/efectos de los fármacos , Guanilil Imidodifosfato/farmacología , Isoproterenol/farmacología , Cinética , PavosAsunto(s)
Adenilil Ciclasas/sangre , Membrana Eritrocítica/metabolismo , Eritrocitos/metabolismo , Nucleótidos de Guanina/sangre , Guanosina Difosfato/sangre , Isoproterenol/farmacología , Receptores de Droga/metabolismo , Animales , AMP Cíclico/sangre , Membrana Eritrocítica/efectos de los fármacos , Guanilil Imidodifosfato/farmacología , Cinética , Receptores de Droga/efectos de los fármacos , PavosAsunto(s)
Infecciones por VIH/metabolismo , VIH-1 , Subgrupos Linfocitarios/metabolismo , Nucleótidos de Purina/metabolismo , Adenina/sangre , Adenosina Difosfato/sangre , Adenosina Trifosfato/sangre , Adulto , Linfocitos T CD4-Positivos/metabolismo , Femenino , Guanina/sangre , Guanosina Difosfato/sangre , Guanosina Trifosfato/sangre , Seropositividad para VIH/sangre , Humanos , Masculino , Persona de Mediana Edad , Subgrupos de Linfocitos T/metabolismoRESUMEN
Metabolism of thiopurine drugs--azathioprine, 6-mercaptopurine, and 6-thioguanine--has provided a powerful pharmacogenetic model incorporating polymorphism of the enzyme thiopurine methyltransferase (TPMT) and the primary active metabolite, thioguanine nucleotide (TGN). However, a sense of uncertainty about the usefulness of TGNs and other thiopurine metabolites has appeared. This review critically appraises the basis of thiopurine metabolism and reveals the problems and complexities in TGN research. Erythrocyte TGN is used in transplantation medicine and in chronic inflammatory conditions such as Crohn's disease, as a "surrogate" pharmacokinetic parameter for TGN in the target cells: leukocytes or bone marrow. It is not generally appreciated that erythrocytes do not express the enzyme IMP dehydrogenase and cannot convert mercaptopurine to TGN, which explains some of the confusion in interpretation of erythrocyte TGN measurements. TGN routinely measured in erythrocytes derives from hepatic metabolism. Another concern is that TGN are not generally assayed directly: most methods assay the thiopurine bases. Ion-exchange HPLC and enzymatic conversion of TGNs to nucleosides have been used to overcome this, and may reveal undisclosed roles for an unusual cytotoxic nucleotide, thio-inosine triphosphate, and methylated thiopurines. There appear to be additional interactions between xanthine oxidase and TPMT, and folate and TPMT, that could predict leukopenia. Difficult questions remain to be answered, which may be assisted by technological advances. Prospective TGN studies, long overdue, are at last revealing clearer results.
Asunto(s)
Azatioprina/uso terapéutico , Monitoreo de Drogas/métodos , Guanosina Difosfato/análogos & derivados , Guanosina Trifosfato/análogos & derivados , Mercaptopurina/uso terapéutico , Tioguanina/uso terapéutico , Tionucleótidos/sangre , Azatioprina/metabolismo , Guanosina Difosfato/sangre , Guanosina Trifosfato/sangre , Humanos , Leucopenia/inducido químicamente , Mercaptopurina/metabolismo , Metilación , Metiltransferasas/genética , Náusea/inducido químicamente , Tioguanina/metabolismo , Xantina Oxidasa/fisiologíaRESUMEN
BACKGROUND & AIMS: Azathioprine is the gold standard for immunosuppressive therapy in Crohn's disease (CD) and its molecular mechanism of action is caused by the metabolite 6-thioguanosine triphosphate (TGTP). In this study we assessed the impact of TGTP levels for monitoring of azathioprine therapy. METHODS: A novel, highly sensitive assay was established to measure levels of TGTP and its precursors 6-thioguanosine monophosphates and 6-thioguanosine diphosphates (TGDP) in red blood cells from 50 CD patients. The results were correlated with clinical outcome. RESULTS: TGTP levels could be quantified in 47 patients and a subgroup of these patients showed significantly high levels of TGDP. 6-thioguanine nucleotide (6-TGN) levels showed a significant correlation with TGDP plus TGTP concentrations, suggesting that active TGTP and its inactive precursor TGDP are the main metabolites within 6-TGN. Patients with 6-TGN levels higher than 100 pmol/8x10(8) red blood cells showed better response rates, on average, than patients with lower 6-TGN levels. The subgroup of patients with higher 6-TGN and increased TGDP levels showed a worse outcome with lower response rates, more flares, and higher infliximab demand than patients with high 6-TGN, low TGDP, and predominantly detectable TGTP levels. CONCLUSIONS: This study shows that quantification of TGTP levels can be used to monitor azathioprine therapy in inflammatory bowel disease patients. Furthermore, the data suggest that TGDP levels of more than 15% of total 6-TGN levels may be a useful surrogate parameter to predict poor response in a subgroup of azathioprine-treated patients.
Asunto(s)
Azatioprina/uso terapéutico , Enfermedad de Crohn/sangre , Enfermedad de Crohn/tratamiento farmacológico , Eritrocitos/química , Nucleótidos de Guanina/sangre , Guanosina Difosfato/análogos & derivados , Inmunosupresores/uso terapéutico , Tionucleótidos/sangre , Adulto , Anticuerpos Monoclonales/administración & dosificación , Biomarcadores/sangre , Guanosina Difosfato/sangre , Humanos , InfliximabRESUMEN
A high-performance liquid chromatographic method with on-line postcolumn fluorescence derivatization is described for the simple and sensitive determination of guanine and its nucleosides and nucleotides in human erythrocytes. After deproteinization of the biospecimen, guanine and its nucleosides and nucleotides were separated on a reversed-phase column (TSKgel ODS-120T) by gradient elution with methanol in the aqueous mobile phase consisting of tetra-n-propylammonium phosphate (pH 6.0) and phosphate buffer (pH 6.0). The compounds were then automatically converted into fluorescent derivatives by reaction with phenylglyoxal. This derivatization was selective for guanine-containing compounds. The present method permitted the reliable quantification of GDP and GTP in human erythrocytes. The detection limits (at a signal-to-noise ratio of 3) for guanine and its nucleosides and nucleotides were 3.2-10.0 pmol in a 20-microliters injection volume. The concentrations of GDP and GTP in human erythrocytes were 17.2 +/- 6.2 and 40.2 +/- 5.8 nmol/ml, respectively.
Asunto(s)
Cromatografía Líquida de Alta Presión/métodos , Eritrocitos/química , Nucleótidos de Guanina/sangre , Guanina/sangre , Fenilglioxal , Adulto , Tampones (Química) , Femenino , Guanosina Difosfato/sangre , Guanosina Trifosfato/sangre , Humanos , Indicadores y Reactivos , Masculino , Fosfatos , Valores de ReferenciaRESUMEN
The integrity of the erythrocyte (RBC) hexose monophosphate shunt was investigated in a group of 33 healthy elderly individuals by determining their RBC glutathione content, glucose-6-phosphate dehydrogenase activity and glutathione regeneration. When these parameters were compared with those of the controls, 44 young healthy adults, no significant differences were found. This study indicates that the RBC hexose monophosphate shunt in healthy elderly individuals is intact. Factors other than senescence per se should be sought in elderly individuals who exhibit dysfunction of this shunt.
Asunto(s)
Envejecimiento , Eritrocitos/enzimología , Vía de Pentosa Fosfato , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Glutatión/sangre , Glutatión Reductasa/sangre , Glutatión Transferasa/sangre , Guanosina Difosfato/sangre , Humanos , Masculino , Persona de Mediana EdadRESUMEN
Capillary electrophoresis proved to be a useful technique for the analysis of intracellular levels of 6-thioguanosine mono-, di-, and triphosphate with analysis times of 20 min. Conditions required for baseline separation of the thioguanine nucleotides consisted of a 25 mM KH2PO4 (pH 8.0) buffer and a separation voltage of +28 kV. Laser-induced fluorescence detection (lambda ex = 325 nm, lambda em = 410 nm) of the thioguanine nucleotide metabolites of 6-mercaptopurine (6-MP) was possible following oxidation of the thiol functionality. Tedious extraction procedures involving mercury cellulose resins or phenyl mercury adduct formation, which had been required previously for the selective extraction of thiopurines from erythrocytes, were unnecessary due to the overall specificity of the approach. However, the inclusion of 50 mM EDTA in the sample preparation was required to inhibit the anabolic/catabolic enzymatic activity, which was responsible for the degradation of the analytes. The method demonstrated linearity from 5 to 1700 pmol/100 microliters red blood cells for the three analytes (RSDs < or = 8%). The feasibility of the method was demonstrated for the quantitation of 6-thioguanine nucleotides in patients receiving either oral or intravenous 6-MP therapy.
Asunto(s)
Eritrocitos/química , Nucleótidos de Guanina/sangre , Guanosina Difosfato/análogos & derivados , Guanosina Trifosfato/análogos & derivados , Mercaptopurina/metabolismo , Tionucleótidos/sangre , Electroforesis , Fluorescencia , Guanosina Difosfato/sangre , Guanosina Trifosfato/sangre , HumanosRESUMEN
The phosphorylation of eukaryotic initiation factor (eIF) 2 alpha that occurs when rabbit reticulocyte lysate is incubated in the absence of hemin or with poly(I.C) causes inhibition of polypeptide chain initiation by preventing a separate factor (termed RF) from promoting the exchange of GTP for GDP on eIF-2. When lysate was incubated in the presence of hemin and [14C] eIF-2 or [alpha-32P]GTP, we observed binding of eIF-2 and GDP or GTP to 60 S ribosomal subunits that was slightly greater than that bound to 40 S subunits and little binding to 80 S ribosomes. When incubation was in the absence of hemin or in the presence of hemin plus 0.1 microgram/ml poly(I.C), eIF-2 and GDP binding to 60 S subunits was increased 1.5- to 2-fold, that bound to 80 S ribosomes was almost as great as that bound to 60 S subunits, and that bound to 40 S subunits was unchanged. Our data indicate that about 40% of the eIF-2 that becomes bound to 60 S subunits and 80 S ribosomes in the absence of hemin or with poly(I.C) is eIF-2(alpha-P) and suggest that the eIF-2 and GDP bound is probably in the form of a binary complex. The accumulation of eIF-2.GDP on 60 S subunits occurs before binding of Met-tRNAf to 40 S subunits becomes reduced and before protein synthesis becomes inhibited. The rate of turnover of GDP (presumably eIF-2.GDP) on 60 S subunits and 80 S ribosomes in the absence of hemin is reduced to less than 10% the control rate, because the dissociation of eIF-2.GDP is inhibited. Additional RF increases the turnover of eIF-2.GDP on 60 S subunits and 80 S ribosomes to near the control rate by promoting dissociation of eIF-2.GDP but not eIF-2(alpha-P).GDP. Our findings suggest that eIF-2.GTP binding to and eIF-2.GDP release from 60 S subunits may normally occur and serve to promote subunit joining. The phosphorylation of eIF-2 alpha inhibits polypeptide chain initiation by preventing dissociation of eIF-2.GDP from either free 60 S subunits (thus inhibiting subunit joining directly) or the 60 S subunit component of an 80 S initiation complex (thereby blocking elongation and resulting in the dissociation of the 80 S complex).
Asunto(s)
Proteínas Sanguíneas , Nucleótidos de Guanina/sangre , Guanosina Difosfato/sangre , Factores de Iniciación de Péptidos/sangre , Reticulocitos/metabolismo , Ribosomas/metabolismo , Animales , Radioisótopos de Carbono , Factor 2 Eucariótico de Iniciación , Guanosina Trifosfato/sangre , Cinética , Factores de Iniciación de Péptidos/antagonistas & inhibidores , Radioisótopos de Fósforo , Fosforilación , Proteínas/antagonistas & inhibidores , Aminoacil-ARN de Transferencia/sangre , ConejosRESUMEN
Changes of the density, MCV, MCHC, RNA-concentration and the activities of the enzyme G6PD and ASAT due to maturation and aging of rbc were investigated by repeated density gradient separation of these cells during a bleeding anaemia of the rabbit. The mean density of reticulocytes and erythrocytes decreases during the course of the anaemia by 14 and 10 g/l respectively. The difference between the density of both cell types increases from 3 to 6 to 12 g/l during the anaemia. Maturation and aging of rbc are characterized by an increase of the MCHC from 200 to 350 g/l cells and the decrease of MCV by 10-25%. The RNA concentration and the ASAT activity show an almost parallel behaviour in cells of different densities during the anaemia. Remarkable differences are observed between the ASAT activity and the G6PD activity: The G6PD activity decreases mainly during the aging process and almost not during the maturation, while the ASAT activity falls constantly during maturation and aging. As observed in former studies we could distinguish and isolate 4 characteristic populations of reticulocytes in certain density fractions during the anaemia: Normal young reticulocytes, line 2 reticulocytes, megaloreticulocytes and reticulocytes of high density.
Asunto(s)
Anemia/sangre , Envejecimiento Eritrocítico , Eritrocitos/enzimología , Eritropoyesis , Hemorragia/sangre , Animales , Aspartato Aminotransferasas/sangre , Separación Celular , Centrifugación por Gradiente de Densidad , Índices de Eritrocitos , Guanosina Difosfato/sangre , ARN/sangre , Conejos , Factores de TiempoRESUMEN
Unsealed membranes from human erythrocytes bind GTP and GTP analogs according to first order kinetics, a single rate constant being observed. With [35S]GTP gamma S this is 0.15 +/- 0.2 min-1. Treatment of the membranes with detergents decreases binding considerably. Scatchard plots reveal uncomplicated patterns of ligand association, with Kd values of 10.2 +/- 2.3 nM [35S]GTP gamma S, of 18.2 +/- 4.3 nM [alpha-32P]GTP and of 28.6 +/- 3.5 nM [alpha-32P]GDP, respectively. The stoichiometry with the three ligands is strictly comparable, i.e. 65 +/- 7 picomoles/mg of membrane protein. Binding of each labeled nucleotide is competitively inhibited by the other two unlabeled ligands, the inhibition constants being very close to the corresponding Kd values. Metabolic depletion and subsequent repletion of intact erythrocytes result in membrane preparations still active in guanine nucleotide binding, with unmodified Kd values. However, the stoichiometry falls to 35 picomoles/mg protein with the "depleted" erythrocyte membranes and regains higher values (50 picomoles/mg protein) with the "repleted" cell membranes. Accordingly, the "in situ" characterization of guanine nucleotide-binding properties of erythrocyte membranes seems to represent a new tool for monitoring the metabolic state of intact erythrocytes.