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1.
Stem Cells ; 34(10): 2548-2558, 2016 10.
Artículo en Inglés | MEDLINE | ID: mdl-27352824

RESUMEN

Stromal support is critical for lung homeostasis and the maintenance of an effective epithelial barrier. Despite this, previous studies have found a positive association between the number of mesenchymal stromal cells (MSCs) isolated from the alveolar compartment and human lung diseases associated with epithelial dysfunction. We hypothesised that bronchoalveolar lavage derived MSCs (BAL-MSCs) are dysfunctional and distinct from resident lung tissue MSCs (LT-MSCs). In this study, we comprehensively interrogated the phenotype and transcriptome of human BAL-MSCs and LT-MSCs. We found that MSCs were rarely recoverable from the alveolar space in healthy humans, but could be readily isolated from lung transplant recipients by bronchoalveolar lavage. BAL-MSCs exhibited a CD90Hi , CD73Hi , CD45Neg , CD105Lo immunophenotype and were bipotent, lacking adipogenic potential. In contrast, MSCs were readily recoverable from healthy human lung tissue and were CD90Hi or Lo , CD73Hi , CD45Neg , CD105Int and had full tri-lineage potential. Transcriptional profiling of the two populations confirmed their status as bona fide MSCs and revealed a high degree of similarity between each other and the archetypal bone-marrow MSC. 105 genes were differentially expressed; 76 of which were increased in BAL-MSCs including genes involved in fibroblast activation, extracellular matrix deposition and tissue remodelling. Finally, we found the fibroblast markers collagen 1A1 and α-smooth muscle actin were increased in BAL-MSCs. Our data suggests that in healthy humans, lung MSCs reside within the tissue, but in disease can differentiate to acquire a profibrotic phenotype and migrate from their in-tissue niche into the alveolar space. Stem Cells 2016;34:2548-2558.


Asunto(s)
Voluntarios Sanos , Pulmón/citología , Células Madre Mesenquimatosas/citología , Alveolos Pulmonares/citología , Actinas/metabolismo , Anciano , Líquido del Lavado Bronquioalveolar , Diferenciación Celular , Linaje de la Célula , Separación Celular , Análisis por Conglomerados , Colágeno Tipo I/genética , Colágeno Tipo I/metabolismo , Cadena alfa 1 del Colágeno Tipo I , Ensayo de Unidades Formadoras de Colonias , Endoglina/metabolismo , Femenino , Citometría de Flujo , Fluorescencia , Perfilación de la Expresión Génica , Humanos , Trasplante de Pulmón , Masculino , Persona de Mediana Edad , Transcriptoma/genética , Adulto Joven
2.
Biochem Pharmacol ; 31(6): 953-7, 1982 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-7082376

RESUMEN

It is well known to carbohydrate chemists that substituted sugars may undergo facile rearrangement involving the migration of the aglycone from --OH to adjacent --OH. Despite the importance of glycoside conjugates, notably involving glucuronic acid, in the metabolism of xenobiotics, drug metabolism workers have neglected this phenomenon. The potential rearrangement of glucuronides from the biosynthetic C-1 isomers to other positional and stereo-isomers is important, since only 1-O-substituted beta-D-glucosiduronates are substrates for beta-glucuronidase, which is commonly used to identify such conjugates. The intramolecular rearrangement of clofibryl glucuronide has been studied over the pH range 5.2-8.6, by enzymic hydrolysis with beta-glucuronidase, and by HPLC. The amount of clofibric acid released from the conjugate by beta-glucuronidase falls with increasing pH of preincubation above pH 7.4, and this is accompanied by the appearance of three new peaks, each containing both clofibric and glucuronic acids, in the HPLC traces of the incubation mixtures. Similar experiments with three other glucuronides, those of p-nitrophenol, phenolphthalein and 7-hydroxycoumarin, did not show any conversion to beta-glucuronidase resistant forms. The phenomenon of intramolecular rearrangement of ester glucuronides must be considered whenever beta-glucuronidase is used in the analysis of conjugates of carboxylic acids.


Asunto(s)
Glucuronatos , Glucuronidasa , Cromatografía Líquida de Alta Presión , Ácido Clofíbrico , Concentración de Iones de Hidrógeno
3.
Br J Nutr ; 96(3): 523-31, 2006 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-16925858

RESUMEN

Relationships between Se and Hg in erythrocytes, and between these indices and intakes of fish and other foods, were studied as an adjunct to the British National Diet and Nutrition Survey (NDNS) of young people aged 4-18 years. Hg was measured in 965 packed erythrocyte samples by inductively coupled plasma mass spectrometry. Fe measurements permitted the calculation of whole-blood Hg. Erythrocyte and plasma Se, and 7 d weighed dietary intake estimates, were available. Erythrocyte Hg was positively skewed, normalised by log-transformation. It was 20 % higher in girls than boys (3.17 v. 2.65 nmol/l, P=0.004), and increased with age in boys but not girls. It was directly and strongly correlated with erythrocyte or plasma Se. Hg and Se concentrations were directly correlated with fish intake. Certain other food groups were also directly correlated with Se and Hg concentrations, but less strongly than for fish. The strength and consistency of the relationship between erythrocyte Hg and Se suggests an important chemical link. Previous studies suggest that Se protects against the toxicity of Hg, and that fish is an important source of both. No toxic levels of Hg were found, which is reassuring because of the known health benefits of fish consumption, especially oily fish. Hg intakes need to be monitored, especially in women of child-bearing age, to ensure that Food Standards Agency guidelines are met.


Asunto(s)
Antioxidantes/análisis , Contaminantes Ambientales/sangre , Peces , Mercurio/sangre , Selenio/sangre , Adolescente , Distribución por Edad , Animales , Niño , Preescolar , Dieta , Ingestión de Alimentos , Eritrocitos/química , Femenino , Contaminación de Alimentos , Humanos , Masculino , Encuestas Nutricionales , Distribución por Sexo , Reino Unido/epidemiología
4.
Drug Metab Dispos ; 11(2): 97-102, 1983.
Artículo en Inglés | MEDLINE | ID: mdl-6133730

RESUMEN

The urinary metabolites of single doses of clofibric acid (p-chlorophenoxyisobutyric acid), and its ethyl ester, clofibrate, have been investigated in rat, guinea pig, rabbit, dog, cat, ferret, and human volunteers. Human volunteers, rodents, and rabbits given clofibric acid excreted 60-90% of the 14C dose in the urine in 24 hr, and the only metabolite found was the ester glucuronide of clofibric acid, together with small amounts of the unchanged acid. In the dog, cat, and ferret, however, urinary excretion of 14C was much slower (23-39% of dose in 24 hr) and these species all formed the taurine conjugate of clofibric acid, excreted together with the unchanged acid. The ester glucuronide was found in the urine of dog and ferret but not cat. The fate of clofibrate, the ethyl ester of clofibric acid, in rat, guinea pig, rabbit, and man was similar to that of the parent acid. The characterization of the glucuronic acid and taurine conjugates of clofibric acid is described.


Asunto(s)
Clofibrato/análogos & derivados , Clofibrato/metabolismo , Ácido Clofíbrico/metabolismo , Animales , Bilis/metabolismo , Biotransformación , Gatos , Cromatografía en Capa Delgada , Perros , Femenino , Hurones , Glucuronatos/metabolismo , Cobayas , Humanos , Espectroscopía de Resonancia Magnética , Masculino , Espectrometría de Masas , Conejos , Ratas , Ratas Endogámicas , Especificidad de la Especie , Taurina/metabolismo
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