RESUMO
BACKGROUND: Although asthma and allergic rhinitis (AR) are considered to be one syndrome, many questions remain unanswered. Why do some AR patients develop asthma but others do not, and which factors play a role in the development of asthma that have so far not been clearly elucidated. OBJECTIVE: We hypothesize that children with AR who have the Clara cell secretory protein (CC16, secretoglobin 1A1) 38A/38A genotype (rs3741240) have an increased likelihood of developing asthma. METHODS: The study sample included 117 children, with AR, but no asthma diagnosed within the following 5 years, as the control group. Cases group (n=202) included age- and gender-matched children with AR first, and asthma developed 3-5 years later, as the study group. The CC16 genotype was determined by PCR and Sau96I restriction digestion of PCR products. The serum CC16 levels were measured by ELISA. Total serum IgE, allergen specific IgE, eosinophil count and pulmonary function were also measured. RESULTS: In children with rhinitis who develop asthma, the frequencies of the AA genotype were significantly higher than those who did not develop asthma [odds ratio (OR)=2.527; 95% confidence interval (CI)=1.571-4.065; P<0.01]. Serum CC16 levels in the children with rhinitis who develop asthma and carry the AA genotype were significantly lower than those who carry the non-AA genotype and those who did not develop asthma. CONCLUSIONS AND CLINICAL RELEVANCE: Results of this study suggest that CC16 38A/38A genotype plays a role in the development of early asthma in children with AR. Early identification of rhinitis children at risk may assist in designing preventative approach to asthma development.
Assuntos
Asma/complicações , Asma/genética , Predisposição Genética para Doença/genética , Polimorfismo Genético/genética , Rinite Alérgica Perene/complicações , Rinite Alérgica Perene/genética , Uteroglobina/genética , Alelos , Asma/imunologia , Criança , Epitopos/imunologia , Feminino , Frequência do Gene , Genótipo , Humanos , Imunoglobulina E/sangue , Imunoglobulina E/imunologia , Masculino , Testes de Função Respiratória , Rinite Alérgica Perene/imunologia , Uteroglobina/sangueRESUMO
The effects of elevated CO(2) concentrations on the photochemistry, biochemistry and physiology of C(4) photosynthesis were studied in maize (Zea mays L.). Plants were grown at ambient (350 &mgr;L L(-1)) or ca. 3 times ambient (1100 &mgr;L L(-1)) CO(2) levels under high light conditions in a greenhouse for 30 d. Relative to plants grown at ambient CO(2) levels, plants grown under elevated CO(2) accumulated ca. 20% more biomass and 23% more leaf area. When measured at the CO(2) concentration of growth, mature leaves of high-CO(2)-grown plants had higher light-saturated rates of photosynthesis (ca. 15%), lower stomatal conductance (71%), higher water-use efficiency (225%) and higher dark respiration rates (100%). High-CO(2)-grown plants had lower carboxylation efficiencies (23%), measured under limiting CO(2), and lower leaf protein contents (22%). Activities of a number of C(3) and C(4) cycle enzymes decreased on a leaf-area basis in the high-CO(2)-grown plants by 5-30%, with NADP-malate dehydrogenase exhibiting the greatest decrease. In contrast, activities of fructose 1,6-bisphosphatase and ADP-glucose pyrophosphorylase increased significantly under elevated CO(2) condition (8% and 36%, respectively). These data show that the C(4) plant maize may benefit from elevated CO(2) through acclimation in the capacities of certain photosynthetic enzymes. The increased capacity to synthesize sucrose and starch, and to utilize these end-products of photosynthesis to produce extra energy by respiration, may contribute to the enhanced growth of maize under elevated CO(2).
RESUMO
NADP-malic enzyme (NADP-ME, EC 1.1.1.40), a key enzyme in C4 photosynthesis, provides CO2 to the bundle-sheath chloroplasts, where it is fixed by ribulose-1,5-bisphosphate carboxylase/oxygenase. We characterized the isoform pattern of NADP-ME in different photosynthetic species of Flaveria (C3, C3-C4 intermediate, C4-like, C4) based on sucrose density gradient centrifugation and isoelectric focusing of the native protein, western-blot analysis of the denatured protein, and in situ immunolocalization with antibody against the 62-kD C4 isoform of maize. A 72-kD isoform, present to varying degrees in all species examined, is predominant in leaves of C3 Flaveria spp. and is also present in stem and root tissue. By immunolabeling, NADP-ME was found to be mostly localized in the upper palisade mesophyll chloroplasts of C3 photosynthetic tissue. Two other isoforms of the enzyme, with molecular masses of 62 and 64 kD, occur in leaves of certain intermediates having C4 cycle activity. The 62-kD isoform, which is the predominant highly active form in the C4 species, is localized in bundle-sheath chloroplasts. Among Flaveria spp. there is a 72-kD constitutive form, a 64-kD form that may have appeared during evolution of C4 metabolism, and a 62-kD form that is necessary for the complete functioning of C4 photosynthesis.