RESUMEN
Tuberous sclerosis complex (TSC), caused by dominant mutations in either TSC1 or TSC2 tumour suppressor genes is characterized by the presence of brain malformations, the cortical tubers that are thought to contribute to the generation of pharmacoresistant epilepsy. Here we report that tuberless heterozygote Tsc1(+/-) mice show functional upregulation of cortical GluN2C-containing N-methyl-D-aspartate receptors (NMDARs) in an mTOR-dependent manner and exhibit recurrent, unprovoked seizures during early postnatal life (Asunto(s)
Anticonvulsivantes/farmacología
, Epilepsia/tratamiento farmacológico
, Pirazoles/farmacología
, Quinolonas/farmacología
, Receptores de N-Metil-D-Aspartato/antagonistas & inhibidores
, Serina-Treonina Quinasas TOR/genética
, Esclerosis Tuberosa/tratamiento farmacológico
, Proteínas Supresoras de Tumor/genética
, Potenciales de Acción/efectos de los fármacos
, Animales
, Modelos Animales de Enfermedad
, Electroencefalografía
, Epilepsia/genética
, Epilepsia/metabolismo
, Epilepsia/patología
, Regulación de la Expresión Génica
, Heterocigoto
, Humanos
, Masculino
, Ratones
, Ratones Transgénicos
, Microtomía
, Neocórtex/efectos de los fármacos
, Neocórtex/metabolismo
, Neocórtex/patología
, Técnicas de Placa-Clamp
, Receptores de N-Metil-D-Aspartato/genética
, Receptores de N-Metil-D-Aspartato/metabolismo
, Transducción de Señal
, Serina-Treonina Quinasas TOR/metabolismo
, Técnicas de Cultivo de Tejidos
, Esclerosis Tuberosa/genética
, Esclerosis Tuberosa/metabolismo
, Esclerosis Tuberosa/patología
, Proteína 1 del Complejo de la Esclerosis Tuberosa
, Proteínas Supresoras de Tumor/deficiencia
RESUMEN
Dynamic covalent surfactants have been obtained by the reversible condensation of a hydrophobic aldehyde (ended by an ionic tip) with various neutral polyethylene glycol based hydrophilic amines. In water, the duality between the two hydrophilic domains (charged and neutral) leads to their segregation when the surfactants are self-assembled within micelles. Depending on the number of polyethylene glycol units, a core-shell inversion leading to a switching orientation of the ionic tips from the inside to the outside of the micelles has been demonstrated by a combination of scattering techniques. In competition experiments, when several amines of different pKas and hydrophilic polyethylene glycol chains are competing for the same aldehyde, it becomes possible to trigger this core-shell inversion by pH modulation and associated dynamic constitutional reorganization.
RESUMEN
We study by small-angle neutron scattering (SANS) the structure of hyaluronan -lysozyme complexes. Hyaluronan (HA) is a polysaccharide of 9 nm intrinsic persistence length that bears one negative charge per disaccharide monomer (M(mol) = 401.3 g/mol); two molecular weights, M(w) = 6000 and 500,000 Da were used. The pH was adjusted at 4.7 and 7.4 so that lysozyme has a global charge of +10 and +8, respectively. The lysozyme concentration was varied from 3 to 40 g/L at constant HA concentration (10 g/L). At low protein concentration, samples are monophasic, and SANS experiments reveal only fluctuations of concentration, although, at high protein concentration, clusters are observed by SANS in the dense phase of the diphasic samples. In between, close to the onset of the phase separation, a distinct original scattering is observed. It is characteristic of a rod-like shape, which could characterize "single" complexes involving one or a few polymer chains. For the large molecular weight (500,000), the rodlike rigid domains extend to much larger length scale than the persistence length of the HA chain alone in solution and the range of the SANS investigation. They can be described as a necklace of proteins attached along a backbone of diameter of one or a few HA chains. For the short chains (M(w) ≈ 6000), the rod length of the complexes is close to the chain contour length (â¼ 15 nm).
Asunto(s)
Electrólitos/química , Ácido Hialurónico/química , Muramidasa/química , Peso MolecularRESUMEN
Dynamers based on reversible Diels-Alder chemistry have been obtained and shown to undergo dynamic exchange at room temperature. Their study in solution by small-angle neutron scattering indicated the formation of long and highly flexible chains. Polydispersed molecules gave T(g) values below room temperature, permitting the generation of a dynamic elastomer upon introduction of a dynamic cross-linking agent. The use of a system with a low equilibrium constant gives access to materials with interesting self-healing properties.
RESUMEN
European ethical and legal positions with regard to EN vary slightly from country to country but are based on a common tradition derived from Graeco Roman ideas, religious thought and events of the 20th century. The Hippocratic tradition is based on 'beneficience' (do good) and 'non-maleficience' (do no harm). Religious thinking is based upon the presumption of providing food and drink by whatever means unless burden outweighs benefit. The concept of 'autonomy' (the patients right to decide) arose following in the decades after the Second World War and is enshrined in Human Rights law. The competent patient has the right to participate in decision making and to refuse treatment although the doctor is not obliged to give treatment which he or she considers futile or against the patient's interests. The incompetent patient is protected by law. The fourth principle is that of 'justice' i.e. equal access to healthcare for all. The law regards withholding and withdrawing treatment as the same. It also defines the provision of food and drink by mouth as basic care and feeding by artificial means as a medical treatment. It requires doctors to act in the best interests of the patient.
Asunto(s)
Nutrición Enteral/ética , Nutrición Enteral/normas , Ética Médica , Eutanasia Pasiva , Autonomía Personal , Toma de Decisiones , Europa (Continente) , Eutanasia Pasiva/ética , Eutanasia Pasiva/legislación & jurisprudencia , Humanos , Legislación Médica , Obligaciones Morales , Pronóstico , Negativa del Paciente al TratamientoRESUMEN
The reasons for the cellular specificity and slow progression of motoneuron diseases such as ALS are still poorly understood. We previously described a motoneuron-specific cell death pathway downstream of the Fas death receptor, in which synthesis of nitric oxide (NO) is an obligate step. Motoneurons from ALS model mice expressing mutant SOD1 showed increased susceptibility to exogenous NO as compared with controls. Here, we report a signaling mechanism whereby NO leads to death of mutant, but not control, motoneurons. Unexpectedly, exogenous NO triggers expression of Fas ligand (FasL) in cultured motoneurons. In mutant SOD1(G93A) and SOD1(G85R), but not in control motoneurons, this up-regulation results in activation of Fas, leading through Daxx to phosphorylation of p38 and further NO synthesis. This Fas/NO feedback amplification loop is required for motoneuron death in vitro. In vivo, mutant SOD1(G93A) and SOD1(G85R) mice show increased numbers of positive motoneurons and Daxx nuclear bodies weeks before disease onset. Moreover, FasL up-regulation is reduced in the presence of transgenic dominant-negative Daxx. We propose that chronic low-level activation of the Fas/NO feedback loop may underlie the motoneuron loss that characterizes familial ALS and may help to explain its slowly progressive nature.
Asunto(s)
Proteínas Portadoras/fisiología , Péptidos y Proteínas de Señalización Intracelular/fisiología , Glicoproteínas de Membrana/fisiología , Enfermedad de la Neurona Motora/fisiopatología , Neuronas Motoras/fisiología , Proteínas Nucleares/fisiología , Factores de Necrosis Tumoral/fisiología , Receptor fas/fisiología , Animales , Proteínas Portadoras/genética , Proteínas Co-Represoras , Cruzamientos Genéticos , Proteína Ligando Fas , Retroalimentación , Femenino , Homocigoto , Péptidos y Proteínas de Señalización Intracelular/genética , Masculino , Glicoproteínas de Membrana/genética , Ratones , Ratones Endogámicos C57BL , Ratones Mutantes , Ratones Transgénicos , Modelos Animales , Chaperonas Moleculares , Enfermedad de la Neurona Motora/genética , Enfermedad de la Neurona Motora/patología , Óxido Nítrico/fisiología , Proteínas Nucleares/genética , Reacción en Cadena de la Polimerasa , Polimorfismo de Nucleótido Simple , Médula Espinal/patología , Médula Espinal/fisiopatología , Superóxido Dismutasa/genética , Superóxido Dismutasa-1 , Factores de Necrosis Tumoral/genética , Receptor fas/genéticaRESUMEN
The structural and dynamic properties of low ionic strength micellar solutions of the cationic surfactant perfluorooctylbutane trimethylammonium bromide have been investigated by cryo-TEM, small-angle neutron scattering, small-angle X-ray scattering, T-jump and rheological experiments. The surfactant molecules self-assemble into narrow ribbons with average dimensions on the order of 4 nm x 3 nm, either under salt-free conditions or in the presence of up to 30 mM KBr or NaF. Cryo-TEM also reveals in the salt-free systems the presence of networks of multiconnected micelles. Rheological experiments showed that these surfactant systems exhibit a strong shear-thickening effect even in the presence of up to 30 mM KBr. The T-jump response of the micellar solutions was found to be multiexponential. This observation rules out the presence of only linear micelles with an exponential length distribution and suggests more complex topologies of the micellar aggregates. The relaxation time associated with the predominant process in the T-jump relaxation is strongly correlated to the critical shear rate beyond which shear thickening occurs, thus indicating that this critical shear rate is controlled by the micellar kinetics.
RESUMEN
The effect of polyelectrolyte addition on the properties of an oil-in-water (O/W) microemulsion of weakly charged spherical micelles is studied. The 81 A radius O/W droplets in this system can be charged by the partial substitution of the nonionic surfactant by a cationic surfactant. The effect of the addition of poly(acrylic acid) (PAA), which is a charged pH-dependent polyelectrolyte, on the interactions between charged or noncharged droplets has been investigated using SANS. We have characterized the phase behavior of this pH-smart system as a function of the microemulsion and the polyelectrolyte concentration and the number of charges per droplet at three pH values: pH = 2, 4.5, and 12. In particular, an associative phase separation due to the bridging of the droplets by the neutral PAA chains through H-bonds is observed with extremely low PAA addition at low pH. At the opposite, an addition of PAA at pH = 4.5 generates a strong repulsive contribution between neutral droplets. Electrostatic bonds between charged droplets and PAA, controlled by the number of charges per droplet, are responsible for a pH drift and then for an associative phase separation similar to that observed at low pH. Finally, at high pH, the creation of electrostatic bonds between fully charged PAA and charged droplets liberates sufficiently counterions in solution at high droplet charge density to screen the electrostatic interactions and to allow an associative phase separation.
RESUMEN
Mammalian spinal motoneurons are cholinergic neurons that have long been suspected to use also glutamate as a neurotransmitter. We report that VGLUT1 and VGLUT2, two subtypes of vesicular glutamate transporters, are expressed in rat spinal motoneurons. Both proteins are present in somato-dendritic compartments as well as in axon terminals in primary cultures of immunopurified motoneurons and sections of spinal cord from adult rat. However, VGLUT1 and VGLUT2 are not found at neuromuscular junctions of skeletal muscles. After intracellular injection of biocytin in motoneurons, VGLUT2 is observed in anterogradely labelled terminals contacting Renshaw inhibitory interneurons. These VGLUT2- and VGLUT1-positive terminals do not express VAChT, the vesicular acetylcholine transporter. Overall, our study establishes for the first time that (i) mammalian spinal motoneurons express vesicular glutamate transporters, (ii) these motoneurons have the potential to release glutamate (in addition to acetylcholine) at terminals contacting Renshaw cells, and finally (iii) the VGLUTs are not present at neuromuscular synapses of skeletal muscles.
Asunto(s)
Neuronas Motoras/fisiología , Médula Espinal/fisiología , Sinapsis/fisiología , Animales , Tronco Encefálico/fisiología , Cartilla de ADN , Inmunohistoquímica , Hibridación in Situ , Proteínas de Transporte de Membrana , Unión Neuromuscular/fisiología , ARN/genética , ARN/aislamiento & purificación , ARN Mensajero/genética , Ratas , Ratas Wistar , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Proteína 1 de Transporte Vesicular de Glutamato , Proteína 2 de Transporte Vesicular de GlutamatoRESUMEN
The mixed micellization between the cationic gemini surfactant [C12H25(CH3)2N+(C2H4)N+(CH3)2C12H25*2Br-] and the cationic cetyltrimethylammonium bromide (CTAB) in 150 mM KBr solutions has been investigated. The variation of the cmc of the mixtures, measured by surface tension experiments, with composition revealed synergism in micelle formation. T-Jump and light scattering experiments performed in the vicinity of the crossover volume fraction showed the existence of two micellar populations, possibly linear and toroidal micelles. Rheological and dynamic light scattering experiments allowed to fully characterize the linear viscoelasticity of the mixtures. These measurements revealed synergistic gains in viscoelastic properties with a maximum of the stress-relaxation time around the equimolar composition. These effects are ascribed to a progressive intermicellar crosslinking resulting from a continuous increase of the end-cap energy with the 12-2-12 content in the mixture.
Asunto(s)
Compuestos de Cetrimonio/química , Mezclas Complejas/química , Canales Iónicos/química , Micelas , Modelos Químicos , Compuestos de Amonio Cuaternario/química , Tensoactivos/química , Sitios de Unión , Cationes/química , Cetrimonio , Coloides/química , Simulación por Computador , Dimerización , Elasticidad , Sustancias Macromoleculares , Conformación Molecular , Tensión Superficial , ViscosidadRESUMEN
In a SANS experiment, we have directly determined for the first time the conformation of hyaluronan, a model semirigid polyelectrolyte. At high ionic strength, this is completely possible, where the scattered intensity crosses over (when decreasing q) from a q(-1) rod variation to a q(-2) and, where fitting to the "wormlike" chain model gives the backbone, intrinsic, persistence length: L0 = 86.5 A. At low ionic strength, we can safely check that the measured persistence length appears increased by at least the amount predicted by Odijk for the electrostatic contribution, L(e) (approximately kappa(-2), square of the Debye screening length). However, the intensity at the lowest q is not only due to the single chain, since it crosses over from a q(-1) to a q(-4) variation, characteristic of polymer associations.
RESUMEN
We present clinical and cytogenetic data of a one year old boy with partial monosomy for both 21q and 18p, resulting from a de novo unbalanced translocation. The initial diagnosis of a seemingly full monosomy 21 was revised after fluorescence in situ hybridisation (FISH) with whole chromosome painting probes and a locus-specific chromosome 21 probe. The karyotype was reinterpreted as 45,XY,der(18)t(18;21)(p11.2;q22.1),-21. This karyotype, to our knowledge, has not been previously described. The boy presented with a spectrum of clinical features previously described for (partial) monosomy 18p only, for monosomy 21q only, or for both of these aneusomies. The radiological finding of a neuronal migration disorder with localised polymicrogyria (cortical dysplasia) has not been described for either monosomy before.
Asunto(s)
Movimiento Celular/genética , Cromosomas Humanos Par 18 , Cromosomas Humanos Par 21 , Monosomía/genética , Neuronas/citología , Translocación Genética , Anomalías Múltiples/genética , Corteza Cerebral/patología , Humanos , Hibridación Fluorescente in Situ , Recién Nacido , Cariotipificación , Imagen por Resonancia Magnética , MasculinoRESUMEN
The Roberts-SC phocomelia syndrome is a rare autosomal recessive inherited disorder clinically manifested by tetraphocomelia, pre- and postnatal growth retardation, and craniofacial abnormalities (skull, eyes, lip, and palate), accompanied at times by centromer puffing and splitting, renal abnormalities, heart defect, clitoral or penile enlargement, and bilateral corneal opacities. Mental retardation is common in surviving patients.
Asunto(s)
Anomalías Múltiples/genética , Aberraciones Cromosómicas/genética , Ectromelia/genética , Genes Recesivos/genética , Anomalías Múltiples/diagnóstico por imagen , Aborto Eugénico , Adulto , Centrómero/genética , Bandeo Cromosómico , Trastornos de los Cromosomas , Diagnóstico Diferencial , Ectromelia/diagnóstico por imagen , Femenino , Humanos , Recién Nacido , Embarazo , Síndrome , Ultrasonografía PrenatalRESUMEN
An X chromosome gene is assumed to be responsible for the cause of Rett syndrome (RS). However, new genealogical observations suggest involvement of autosomal recessive gene(s) as well, at least in familial cases. To account for these and other recent observations, the theoretical model presented in 1990 by the authors of this paper is applied to the calculation of gene frequencies. Observed frequencies of sporadic and familial cases of RS are used, taking into account genetic drift in inbreeded areas. Moreover, an attempt is made to use the proportion of RS variants in familial and sporadic cases for the explanation of so called 'formes frustes', and as evidence for the existence of female as well as male carriers. The estimated frequency of the recessive autosome mutation, or possibly a frequent polymorphism, is 22.5%.
Asunto(s)
Frecuencia de los Genes , Síndrome de Rett/genética , Cromosoma X , Alelos , Femenino , Genes Recesivos , Tamización de Portadores Genéticos , Impresión Genómica , Genotipo , Humanos , Masculino , Modelos GenéticosRESUMEN
Absolute specificity and high accuracy is required for the quantitation of cholesterol, cholesteryl esters and triglycerides in small biological samples, particularly in a limited number of cells. Both can be achieved through thin-layer chromatography and molybdatophosphoric acid staining, while the shortcomings of traditional spot detection are overcome by laser densitometry. The major advantage of the proposed technique is the concurrent assay of nanogram quantities of cholesterol, cholesteryl esters and triglycerides. Our assay is at least ten-fold more sensitive than common thin-layer chromatography-based techniques and at least four-fold more sensitive than common enzymatic methods. The present low-cost assay is highly reproducible and may be particularly suitable for the routine lipid analysis of a 10% aliquot of relatively small tissue and cell samples, equivalent, for instance, to > or = 10(4) human monocytes.
Asunto(s)
Ésteres del Colesterol/sangre , Colesterol/sangre , Cromatografía en Capa Delgada/métodos , Leucocitos Mononucleares/química , Triglicéridos/sangre , Densitometría , Humanos , Rayos Láser , Masculino , Microquímica , Persona de Mediana Edad , Reproducibilidad de los Resultados , Sensibilidad y EspecificidadRESUMEN
We report on a boy with mosaic trisomy 15. The clinical manifestations are compared with those of the few cases reported up to now. A clinical syndrome is delineated consisting of a characteristic shape of the nose and other minor craniofacial anomalies, as well as typical deformities of the hands and feet. Different degrees of mosaicism may explain the more or less severe manifestations in individual patients.
Asunto(s)
Anomalías Múltiples/genética , Cromosomas Humanos Par 15 , Mosaicismo , Trisomía , Adulto , Células Cultivadas , Preescolar , Femenino , Fibroblastos/citología , Humanos , Masculino , Embarazo , SíndromeRESUMEN
Decreased mitogen responsiveness of lymphocytes during aging correlates inversely with membrane microviscosity, which reflects an altered lipid composition. Therefore, we addressed the question, whether age-related alterations of lipid metabolism affect the switch in lipid composition during formation of blasts. Membrane lipids and fatty acids of peripheral blood lymphocytes from SENIEUR protocol compatible ("healthy") elderly donors (66-77 yr) and young controls (18-30 yr) were quantified after incubation with or without the mitogen phytohaemagglutinin. The blastic change in membrane lipid composition was different for young controls with respect to cholesterol, phosphatidylethanolamine, total phospholipids, as well as several fatty acids. Moreover, the age-related alterations in the switch of membrane lipids and fatty acids were significantly correlated with a decreased mitogen response. Thus, the alterations in membrane reorganization during blast formation of lymphocytes from the elderly point to a disturbed cellular lipid homeostasis with possible impact on the age-related reduction in immune function.
Asunto(s)
Envejecimiento/inmunología , Metabolismo de los Lípidos , Activación de Linfocitos , Linfocitos/metabolismo , Adolescente , Adulto , Anciano , Envejecimiento/metabolismo , Ácidos Grasos/metabolismo , Humanos , Linfocitos/efectos de los fármacos , Linfocitos/fisiología , Masculino , Lípidos de la Membrana/metabolismo , Mitógenos/farmacología , Valores de Referencia , ViscosidadRESUMEN
A rare instance of double heterozygosity for spondyloepiphyseal dysplasia congenita and achondroplasia is presented. Despite midface hypoplasia, thorax deformity and lung hypoplasia, the child survived the neonatal period. Severe pulmonary hypertension, already present at birth, led to right heart failure and death at the age of 1 year.