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1.
J Clin Microbiol ; 52(8): 3075-7, 2014 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-24899024

RESUMEN

In remote countries, leptospirosis confirmation is difficult because it requires the shipment of frozen samples to reference laboratories. The sensitivity of leptospirosis real-time PCR performed on filter paper-dried serum samples stored at ambient temperature was evaluated at 2 × 10(2) equivalent leptospires/ml (eqLeptospires/ml). This easy alternative procedure can be used to enhance the surveillance of leptospirosis.


Asunto(s)
Desecación , Leptospirosis/diagnóstico , Técnicas de Diagnóstico Molecular/métodos , Reacción en Cadena en Tiempo Real de la Polimerasa/métodos , Manejo de Especímenes/métodos , Humanos , Papel , Sensibilidad y Especificidad , Temperatura
2.
Cereb Cortex ; 22(2): 403-16, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-21666133

RESUMEN

The relative contribution of intrinsic and extrinsic cues in the regulation of cortical neurogenesis remains a crucial challenge in developmental neurobiology. We previously reported that a transient population of glutamatergic neurons, the cortical plate (CP) transient neurons, migrates from the ventral pallium (VP) over long distances and participate in neocortical development. Here, we show that the genetic ablation of this population leads to a reduction in the number of cortical neurons especially fated to superficial layers. These defects result from precocious neurogenesis followed by a depletion of the progenitor pools. Notably, these changes progress from caudolateral to rostrodorsal pallial territories between E12.5 and E14.5 along the expected trajectory of the ablated cells. Conversely, we describe enhanced proliferation resulting in an increase in the number of cortical neurons in the Gsx2 mutants which present an expansion of the VP and a higher number of CP transient neurons migrating into the pallium. Our findings indicate that these neurons act to maintain the proliferative state of neocortical progenitors and delay differentiation during their migration from extraneocortical regions and, thus, participate in the extrinsic control of cortical neuronal numbers.


Asunto(s)
Movimiento Celular/fisiología , Corteza Cerebral , Glutamatos/metabolismo , Células-Madre Neurales/fisiología , Neurogénesis/genética , Neuronas/fisiología , Factores de Edad , Animales , Animales Recién Nacidos , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/genética , Tipificación del Cuerpo/genética , Bromodesoxiuridina/metabolismo , Cadherinas/metabolismo , Ciclo Celular/genética , Diferenciación Celular , Movimiento Celular/genética , Proliferación Celular , Corteza Cerebral/citología , Corteza Cerebral/embriología , Corteza Cerebral/crecimiento & desarrollo , Ventrículos Cerebrales/citología , Ventrículos Cerebrales/embriología , Ventrículos Cerebrales/crecimiento & desarrollo , Embrión de Mamíferos , Regulación del Desarrollo de la Expresión Génica , Proteínas Fluorescentes Verdes/genética , Proteínas de Homeodominio/genética , Proteínas de Homeodominio/metabolismo , Factores de Transcripción MEF2 , Ratones , Ratones Endogámicos C57BL , Ratones Transgénicos , Mutación/genética , Factores Reguladores Miogénicos/metabolismo , Proteínas del Tejido Nervioso/genética , Proteínas del Tejido Nervioso/metabolismo , Proteínas Nucleares/metabolismo , Miembro 1 del Grupo C de la Subfamilia 2 de Receptores Nucleares/metabolismo , Proteínas Represoras/metabolismo
4.
Clin Microbiol Infect ; 23(12): 1001.e1-1001.e3, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-28711704

RESUMEN

OBJECTIVES: Zika virus (ZIKV) transmission through semen donation has never been reported but the risk is supported by the detection of ZIKV in semen and the demonstration of ZIKV sexual transmission. The potential impact of ZIKV on assisted reproductive procedures should be evaluated. METHODS: We tested longitudinally collected semen samples provided by asymptomatic blood donors who tested positive for ZIKV RNA in plasma during ZIKV outbreaks in Puerto Rico and Florida in 2016. RESULTS: Five of the 14 (35.7%) asymptomatic blood donors provided semen samples that tested positive for ZIKV RNA, with ZIKV RNA loads ranging from 8.03 × 103 to 2.55 × 106 copies/mL. Plasma collected at the same time as the semen tested negative for ZIKV RNA for most ZIKV RNA-positive semen collections; all corresponding plasma samples tested positive or equivocal for anti-ZIKV IgG antibodies and all except one tested positive for ZIKV IgM antibodies. The rate of detection of ZIKV RNA in semen in asymptomatic donors is not significantly different from the rate previously reported for symptomatic patients. CONCLUSIONS: Our results that show a high percentage of detection of ZIKV RNA in the semen of asymptomatic men confirm that ZIKV is a new threat for reproductive medicine and should have important implications for assisted reproductive technology. We recommend that semen donations from men at risk for ZIKV infection should be tested for ZIKV RNA, regardless of symptoms of ZIKV infection.


Asunto(s)
Donantes de Sangre , ARN Viral/genética , Semen/microbiología , Infección por el Virus Zika/diagnóstico , Virus Zika/genética , Infecciones Asintomáticas , Donantes de Sangre/estadística & datos numéricos , Florida/epidemiología , Humanos , Masculino , Puerto Rico/epidemiología , Semen/química , Infección por el Virus Zika/epidemiología
5.
Neuroscience ; 167(3): 724-34, 2010 May 19.
Artículo en Inglés | MEDLINE | ID: mdl-20188149

RESUMEN

The different origins of Cajal-Retzius cells (CRc) as well as their diverse molecular profile suggest that this cell type may represent different neuronal subpopulations. In order to investigate whether CRc from different origins show distinct functional or morphological characteristics we used transgenic Dbx1(cre);ROSA26(YFP) mice in which two subpopulations of CRc, originating from the septum and ventral pallium (VP) at the pallial-subpallial border (PSB), were permanently labeled by yellow fluorescent protein (YFP) expression. Electrophysiological properties of YFP(+) and YFP(-) CRc were investigated by whole-cell patch-clamp recordings, while a thorough somatodendritic and axonal reconstruction of the biocytin labeled CRc was subsequently performed using a Neurolucida system. Our experiments revealed that no significant differences in resting membrane potential, input resistance or capacitance, hyperpolarization activated currents and most action potentials properties could be observed between YFP(+) and YFP(-) CRc. Both YFP(+) and YFP(-) CRc displayed spontaneous and carbachol-induced GABAergic postsynaptic currents with similar properties and comparable NMDA-receptor mediated glutamatergic inward currents that were equally affected by the NR2B specific antagonist ifenprodil. Morphological reconstructions revealed that dendritic and axonal parameters are similar between YFP(+) and YFP(-) CRc, while the dendritic compartment of YFP(+) CRc was slightly larger. In summary, no considerable differences in functional and morphological properties between YFP(+) and YFP(-) CRc could be observed in this study. These observations suggest that CRc of different ontogenic origins display comparable functional properties in the early postnatal cortex and therefore perform similar functions within the transient neuronal networks of the developing cortex.


Asunto(s)
Diferenciación Celular/fisiología , Corteza Cerebral/citología , Corteza Cerebral/crecimiento & desarrollo , Neurogénesis/fisiología , Neuronas/citología , Células Madre/citología , Potenciales de Acción/fisiología , Animales , Linaje de la Célula/fisiología , Forma de la Célula/fisiología , Corteza Cerebral/metabolismo , Dendritas/fisiología , Dendritas/ultraestructura , Antagonistas de Aminoácidos Excitadores/farmacología , Ácido Glutámico/metabolismo , Citometría de Imagen , Proteínas Luminiscentes/genética , Proteínas Luminiscentes/metabolismo , Potenciales de la Membrana/fisiología , Ratones , Ratones Transgénicos , Red Nerviosa/citología , Red Nerviosa/crecimiento & desarrollo , Red Nerviosa/metabolismo , Neuronas/metabolismo , Técnicas de Cultivo de Órganos , Técnicas de Placa-Clamp , Receptores de N-Metil-D-Aspartato/antagonistas & inhibidores , Receptores de N-Metil-D-Aspartato/metabolismo , Células Madre/metabolismo , Ácido gamma-Aminobutírico/metabolismo
6.
Gerontology ; 47(4): 207-12, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11408726

RESUMEN

Although weight, lean mass, fat mass and muscular strength are often found to be intercorrelated, the respective role of each parameter in bone mineral density (BMD) remains unknown in older women. The aim of the present study was to investigate the relationship between body weight and composition and quadriceps strength on femoral neck and lumbar spine BMD in healthy postmenopausal women. The relationship between isokinetic quadriceps strength measured by Biodex and BMD measured by dual energy X-ray absorptiometry was studied in 56 women aged 60-81 (70.5 +/- 6.2) years in multiple regression models adjusted for age, body composition and menopausal treatment. Weight and age were associated with femoral neck BMD (33 and 10% of variance accounted for, respectively) and lumbar spine BMD (23 and 8% of its variance). When body weight and quadriceps strength were excluded from the model, lean mass and age were associated with femoral neck BMD (29 and 14% of variance explained, respectively) and lumbar spine BMD (28 and 11% of variance explained, respectively). When quadriceps strength was entered into the model, it was strongly associated with femoral neck BMD (30% of variance accounted for), in addition to lean mass (9%) and age (7%), whereas it was not associated with lumbar spine BMD. In conclusion, lean mass explains a great part of the strong association between body weight and femoral neck and lumbar spine BMD. Quadriceps strength explains a great part of the association between lean mass and BMD at the femoral neck site but not at the lumbar spine site. These results suggest a site-specific effect of muscular strength on bone and a potential role of the age-related decline of muscle strength in age-related bone loss in postmenopausal women.


Asunto(s)
Composición Corporal/fisiología , Peso Corporal/fisiología , Densidad Ósea/fisiología , Músculo Esquelético/fisiología , Factores de Edad , Anciano , Anciano de 80 o más Años , Ejercicio Físico/fisiología , Femenino , Cuello Femoral/fisiología , Humanos , Estilo de Vida , Vértebras Lumbares/fisiología , Persona de Mediana Edad , Posmenopausia/fisiología , Valores de Referencia
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