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BACKGROUND: Parental allergic diseases and smoking influence respiratory disease in the offspring but it is not known whether they influence fractional exhaled nitric oxide (FeNO) in the offspring. We investigated whether parental allergic diseases, parental smoking and FeNO levels in parents were associated with FeNO levels in their offspring. METHODS: We studied 609 offspring aged 16-47 years from the Respiratory Health in Northern Europe, Spain and Australia generation (RHINESSA) study with parental information from the Respiratory Health in Northern Europe (RHINE) III study and the European Community Respiratory Health Survey (ECRHS) III. Linear regression models were used to assess the association between offspring FeNO and parental FeNO, allergic rhinitis, asthma and smoking, while adjusting for potential confounding factors. RESULTS: Parental allergic rhinitis was significantly associated with higher FeNO in the offspring, both on the paternal and maternal side (percent change: 20.3 % [95%CI 5.0-37.7], p = 0.008, and 13.8 % [0.4-28.9], p = 0.043, respectively). Parental allergic rhinitis with asthma in any parent was also significantly associated with higher offspring FeNO (16.2 % [0.9-33.9], p = 0.037). However, parental asthma alone and smoking were not associated with offspring FeNO. Parental FeNO was not associated with offspring FeNO after full adjustments for offspring and parental factors. CONCLUSIONS: Parental allergic rhinitis but not parental asthma was associated with higher levels of FeNO in offspring. These findings suggest that parental allergic rhinitis status should be considered when interpreting FeNO levels in offspring beyond childhood.
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Asma , Óxido Nítrico , Rinitis Alérgica , Fumar , Humanos , Femenino , Masculino , Asma/metabolismo , Rinitis Alérgica/metabolismo , Adolescente , Óxido Nítrico/análisis , Óxido Nítrico/metabolismo , Adulto , Persona de Mediana Edad , Fumar/efectos adversos , Adulto Joven , PadresRESUMEN
Plants possess specific signaling pathways, such as the MultiStep Phosphorelay (MSP), which is involved in cytokinin and ethylene sensing, and light, drought or osmotic stress sensing. These MSP comprise histidine-aspartate kinases (HKs) as receptors, histidine phosphotransfer (HPts) proteins acting as phosphorelay proteins, and response regulators (RRs), some of which act as transcription factors (type-B RRs). In previous studies, we identified partners of the poplar osmosensing signaling pathway, composed of two HKs, three main HPts, and six type-B RRs. To date, it is unresolved as to how cytokinin or osmotic stress signal specificity is achieved in the MSP in order to generate specific responses. Here, we present a large-scale interaction study of poplar type-B RR dimerization. Using the two-hybrid assay, we were able to show the homodimerization of type-B RRs, the heterodimerization of duplicated type-B RRs, and surprisingly, a lack of interaction between some type-B RRs belonging to different duplicates. The lack of interaction of the duplicates RR12-14 and RR18-19, which are involved in the osmosensing pathway has been confirmed by BiFC experiments. This study reveals, for the first time, an overview of type-B RR dimerization in poplar and makes way for the hypothesis that signal specificity for cytokinin or osmotic stress could be in part due to the fact that it is impossible for specific type-B RRs to heterodimerize.
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Aspartato Quinasa/metabolismo , Reguladores del Crecimiento de las Plantas/genética , Reguladores del Crecimiento de las Plantas/metabolismo , Populus/genética , Populus/metabolismo , Transducción de Señal/genética , Factores de Transcripción/metabolismo , Aspartato Quinasa/genética , Dimerización , Regulación de la Expresión Génica de las Plantas , Genes de Plantas , Variación Genética , Genotipo , Histidina Quinasa/genética , Histidina Quinasa/metabolismo , Presión Osmótica , Transducción de Señal/fisiología , Técnicas del Sistema de Dos HíbridosRESUMEN
In this Letter, we show that cross-beam energy transfer (CBET), ubiquitous in inertial confinement fusion (ICF) experiments, may be strongly modified by the speckle pattern of the beams. This is demonstrated by the means of two-dimensional particle in cell simulations, supported by a linear model. In particular, we show that, although they would be the same in a plane wave model, the exchange rates of energy may be significantly different whether there is a plasma flow, or a wavelength shift, especially when the waves are weakly damped. When the crossed laser beams have different frequencies, the energy exchange rate is substantially reduced compared with the predictions of the plane wave model, widely used in the hydrodynamic codes that model and interpret ICF experiments. Such effects can partly explain the disagreement of the CBET predictions compared with experimental results.
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PURPOSE OF REVIEW: The aim of this review is to identify the key contextual and methodological differences in health impact assessments (HIA) of ambient air pollution performed for Europe. We limited our review to multi-country reviews. An additional aim is to quantify some of these differences by applying them in a HIA template in three European cities. RECENT FINDINGS: Several HIAs of ambient air pollution have been performed for Europe, and their key results have been largely disseminated. Different studies have, however, come up with substantial differences in attributed health effects. It is of importance to review the background contributing to these differences and to quantify their importance for decision makers who will use them. We identified several methodological differences that could explain the discrepancy behind the number of attributable deaths or years of life lost. The main differences are due to the exposure-response functions chosen, the ways of assessing air pollution levels, the air pollution scenarios and the study population. In the quantification part, we found that using risk estimates from the European Study of Cohorts for Air Pollution Effects (ESCAPE) instead of the American Cancer Society (ACS) study could nearly double the attributable burden of ambient air pollution. This study provides some insights into the differential results in previously published HIAs on air pollution in Europe. These results are important for stakeholders in order to make informed decisions.
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Contaminación del Aire/efectos adversos , Evaluación del Impacto en la Salud , Contaminación del Aire/análisis , Relación Dosis-Respuesta a Droga , Exposición a Riesgos Ambientales/efectos adversos , Europa (Continente)/epidemiología , Humanos , Medición de RiesgoRESUMEN
Natural compounds extracted from microorganisms or plants constitute an inexhaustible source of valuable molecules whose supply can be potentially challenged by limitations in biological sourcing. The recent progress in synthetic biology combined to the increasing access to extensive transcriptomics and genomics data now provide new alternatives to produce these molecules by transferring their whole biosynthetic pathway in heterologous production platforms such as yeasts or bacteria. While the generation of high titer producing strains remains per se an arduous field of investigation, elucidation of the biosynthetic pathways as well as characterization of their complex subcellular organization are essential prequels to the efficient development of such bioengineering approaches. Using examples from plants and yeasts as a framework, we describe potent methods to rationalize the study of partially characterized pathways, including the basics of computational applications to identify candidate genes in transcriptomics data and the validation of their function by an improved procedure of virus-induced gene silencing mediated by direct DNA transfer to get around possible resistance to Agrobacterium-delivery of viral vectors. To identify potential alterations of biosynthetic fluxes resulting from enzyme mislocalizations in reconstituted pathways, we also detail protocols aiming at characterizing subcellular localizations of protein in plant cells by expression of fluorescent protein fusions through biolistic-mediated transient transformation, and localization of transferred enzymes in yeast using similar fluorescence procedures. Albeit initially developed for the Madagascar periwinkle, these methods may be applied to other plant species or organisms in order to establish synthetic biology platform.
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Catharanthus/enzimología , Catharanthus/genética , Genes de Plantas , Genómica/métodos , Biología Sintética/métodos , Transcriptoma , Levaduras/genética , Vías Biosintéticas , Catharanthus/citología , Catharanthus/metabolismo , Ingeniería Metabólica/métodos , Microscopía Fluorescente/métodos , Transformación Genética , Levaduras/citología , Levaduras/enzimología , Levaduras/metabolismoRESUMEN
Catharanthus roseus constitutes the unique source of several valuable monoterpenoid indole alkaloids, including the antineoplastics vinblastine and vincristine. These alkaloids result from a complex biosynthetic pathway encompassing between 30 and 50 enzymatic steps whose characterisation is still underway. The most recent identifications of genes from this pathway relied on a tobacco rattle virus-based virus-induced gene silencing (VIGS) approach, involving an Agrobacterium-mediated inoculation of plasmids encoding the two genomic components of the virus. As an alternative, we developed a biolistic-mediated approach of inoculation of virus-encoding plasmids that can be easily performed by a simple bombardment of young C. roseus plants. After optimisation of the transformation conditions, we showed that this approach efficiently silenced the phytoene desaturase gene, leading to strong and reproducible photobleaching of leaves. This biolistic transformation was also used to silence a previously characterised gene from the alkaloid biosynthetic pathway, encoding iridoid oxidase. Plant bombardment caused down-regulation of the targeted gene (70%), accompanied by a correlated decreased in MIA biosynthesis (45-90%), similar to results obtained via agro-transformation. Thus, the biolistic-based VIGS approach developed for C. roseus appears suitable for gene function elucidation and can readily be used instead of the Agrobacterium-based approach, e.g. when difficulties arise with agro-inoculations or when Agrobacterium-free procedures are required to avoid plant defence responses.
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Alcaloides/biosíntesis , Catharanthus/genética , Regulación de la Expresión Génica de las Plantas , Silenciador del Gen , Genes de Plantas , Vectores Genéticos , Virus de Plantas , Agrobacterium , Antineoplásicos Fitogénicos/biosíntesis , Vías Biosintéticas/genética , Catharanthus/metabolismo , Genoma Viral , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Plásmidos , Nicotiana/virología , Transformación GenéticaRESUMEN
Involvement of Ca(2+) signalling in regulation of the biosynthesis of monoterpene indole alkaloids (MIA) in Catharanthus roseus has been extensively studied in recent years, albeit no protein of this signalling pathway has been isolated. Using a PCR strategy, two C. roseus cDNAs encoding distinct calmodulin (CAM) isoforms were cloned and named CAM1 and CAM2. The deduced 149 amino acid sequences possess four Ca(2+) binding domains and exhibit a close identity with Arabidopsis CAM isoforms (>91%). The ability of CAM1 and CAM2 to bind Ca(2+) was demonstrated following expression of the corresponding recombinant proteins. Furthermore, transient expression of CAM1-GFP and CAM2-GFP in C. roseus cells showed a typical nucleo-cytoplasm localisation of both CAMs, in agreement with the wide distribution of CAM target proteins. Using RNA blot analysis, we showed that CAM1 and CAM2 genes had a broad pattern of expression in C. roseus organs and are constitutively expressed during a C. roseus cell culture cycle, with a slight inhibitory effect of auxin for CAM1. Using RNA in situ hybridisation, we also detected CAM1 and CAM2 mRNA in the vascular bundle region of young seedling cotyledons. Finally, using specific inhibitors, we also showed that CAMs are required for MIA biosynthesis in C. roseus cells by acting on regulation of expression of genes encoding enzymes that catalyse early steps of MIA biosynthesis, such as 1-deoxy-d-xylulose 5-phosphate reductoisomerase and geraniol 10-hydroxylase.
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Calmodulina/metabolismo , Catharanthus/metabolismo , Proteínas de Plantas/metabolismo , Secuencia de Aminoácidos , Calmodulina/química , Calmodulina/genética , Catharanthus/química , Catharanthus/genética , Línea Celular , Clonación Molecular , Secuencia Conservada , Regulación de la Expresión Génica de las Plantas , Datos de Secuencia Molecular , Proteínas de Plantas/química , Proteínas de Plantas/genética , Isoformas de Proteínas/química , Isoformas de Proteínas/genética , Isoformas de Proteínas/metabolismo , Alineación de SecuenciaRESUMEN
Two periwinkle cDNAs (crdxr and crmecs) encoding enzymes of the non-mevalonate terpenoid pathway were characterized using reverse transcription-PCR strategy based on the design of degenerated oligonucleotides. The deduced amino acid sequence of crdxr is homologue to 1-deoxy-D-xylulose 5-phosphate reductoisomerases. Crmecs represents the first plant cDNA encoding a protein similar to the 2C-methyl-D-erythritol 2,4-cyclodiphosphate synthase from Escherichia coli. Expression of crdxr and crmecs genes was up-regulated in periwinkle cells producing monoterpenoid indole alkaloids. Involvement of the 2C-methyl-D-erythritol 4-phosphate pathway in alkaloid biosynthesis is discussed.
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Isomerasas Aldosa-Cetosa/genética , ADN Complementario/química , Eritritol/metabolismo , Genes de Plantas , Complejos Multienzimáticos/genética , Nucleotidiltransferasas/genética , Oxidorreductasas/genética , Fosfatos de Azúcar/metabolismo , Isomerasas Aldosa-Cetosa/química , Alcaloides , Secuencia de Aminoácidos , Secuencia de Bases , Clonación Molecular , Eritritol/análogos & derivados , Datos de Secuencia Molecular , Complejos Multienzimáticos/química , Nucleotidiltransferasas/química , Oxidorreductasas/química , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Alineación de Secuencia , Homología de Secuencia de AminoácidoRESUMEN
We previously isolated a CD4 ligand glycoprotein, gp17, from human seminal plasma; this glycoprotein is identical with gross cystic disease fluid protein-15 (GCDFP-15), a factor specifically secreted from primary and secondary breast tumors. The function of gp17/GCDFP-15 in physiological as well as in pathological conditions has remained elusive thus far. As a follow up to our previous findings that gp17 binds to CD4 with high affinity and interferes with both HIV-1 gp120 binding to CD4 and syncytium formation, we investigated whether gp17 could affect the T lymphocyte apoptosis induced by a separate ligation of CD4 and TCR. We show here that gp17/GCDFP-15 is in fact a strong and specific inhibitor of the T lymphocyte programmed cell death induced by CD4 cross-linking and subsequent TCR activation. The antiapoptotic effect observed in the presence of gp17 correlates with a moderate up-regulation of Bcl-2 expression in treated cells. The presence of gp17 also prevents the down-modulation of Bcl-2 expression in Bcl-2bright CD4+ T cells that is caused by the triggering of apoptosis. Our results suggest that gp17 may represent a new immunomodulatory CD4 binding factor playing a role in host defense against infections and tumors.
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Apolipoproteínas , Apoptosis/efectos de los fármacos , Neoplasias de la Mama/química , Antígenos CD4/fisiología , Proteínas Portadoras/farmacología , Glicoproteínas , Proteínas de Transporte de Membrana , Proteínas de Neoplasias/farmacología , Receptores de Antígenos de Linfocitos T/fisiología , Vesículas Seminales/química , Adulto , Apolipoproteínas D , Femenino , Humanos , Masculino , Proteínas Proto-Oncogénicas c-bcl-2/análisis , Receptor fas/análisisRESUMEN
IGF-I receptors were characterized in leg and breast muscles from 1- and 7-week-old chickens selected for high (HG) or low (LG) growth rate. Following whole muscle solubilization, receptors were partially purified by wheat germ agglutinin (WGA) chromatography. IGF-I and insulin binding did not differ between genotypes, but significantly decreased with age, without any change in receptor affinity. In the older birds, insulin binding was lower in breast than in leg muscle, whereas IGF-I binding was similar. Using the artificial substrate poly(Glu-Tyr) 4:1, the IGF-I-stimulated tyrosine kinase activity of the receptors was measured and compared between genotypes (at 1 week), and in HG chickens between muscle types (1 and 7 weeks) and ages (in leg muscle). It was not modified by any of these factors. We conclude that: (1) IGF-I and insulin receptor number do not differ between genotypes, (2) the number of both receptors decreases with age, and (3) in 7-week-old birds, breast muscle could become less responsive to insulin than leg muscles, following a decrease in receptor number.