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1.
Nature ; 472(7341): 57-63, 2011 Apr 07.
Artículo en Inglés | MEDLINE | ID: mdl-21475195

RESUMEN

Metabolomics studies hold promise for the discovery of pathways linked to disease processes. Cardiovascular disease (CVD) represents the leading cause of death and morbidity worldwide. Here we used a metabolomics approach to generate unbiased small-molecule metabolic profiles in plasma that predict risk for CVD. Three metabolites of the dietary lipid phosphatidylcholine--choline, trimethylamine N-oxide (TMAO) and betaine--were identified and then shown to predict risk for CVD in an independent large clinical cohort. Dietary supplementation of mice with choline, TMAO or betaine promoted upregulation of multiple macrophage scavenger receptors linked to atherosclerosis, and supplementation with choline or TMAO promoted atherosclerosis. Studies using germ-free mice confirmed a critical role for dietary choline and gut flora in TMAO production, augmented macrophage cholesterol accumulation and foam cell formation. Suppression of intestinal microflora in atherosclerosis-prone mice inhibited dietary-choline-enhanced atherosclerosis. Genetic variations controlling expression of flavin monooxygenases, an enzymatic source of TMAO, segregated with atherosclerosis in hyperlipidaemic mice. Discovery of a relationship between gut-flora-dependent metabolism of dietary phosphatidylcholine and CVD pathogenesis provides opportunities for the development of new diagnostic tests and therapeutic approaches for atherosclerotic heart disease.


Asunto(s)
Enfermedades Cardiovasculares/metabolismo , Enfermedades Cardiovasculares/microbiología , Tracto Gastrointestinal/metabolismo , Tracto Gastrointestinal/microbiología , Fosfatidilcolinas/metabolismo , Animales , Aterosclerosis/inducido químicamente , Aterosclerosis/genética , Aterosclerosis/metabolismo , Aterosclerosis/microbiología , Betaína/sangre , Betaína/metabolismo , Biomarcadores/sangre , Biomarcadores/metabolismo , Enfermedades Cardiovasculares/sangre , Enfermedades Cardiovasculares/diagnóstico , HDL-Colesterol/sangre , Colina/administración & dosificación , Colina/sangre , Colina/metabolismo , Colina/farmacología , Dieta/efectos adversos , Grasas de la Dieta/sangre , Grasas de la Dieta/metabolismo , Grasas de la Dieta/farmacología , Femenino , Regulación de la Expresión Génica , Vida Libre de Gérmenes , Humanos , Hígado/enzimología , Macrófagos/metabolismo , Metabolómica , Metilaminas/sangre , Metilaminas/metabolismo , Metilaminas/farmacología , Ratones , Ratones Endogámicos C57BL , Oxigenasas/genética , Oxigenasas/metabolismo , Fenotipo , Fosfatidilcolinas/administración & dosificación , Fosfatidilcolinas/sangre , Fosfatidilcolinas/farmacología , Receptores Depuradores/metabolismo , Medición de Riesgo
2.
J Immunol ; 186(5): 2871-80, 2011 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-21278342

RESUMEN

Exciting discoveries related to IL-1R/TLR signaling in the development of atherosclerosis plaque have triggered intense interest in the molecular mechanisms by which innate immune signaling modulates the onset and development of atherosclerosis. Previous studies have clearly shown the definitive role of proinflammatory cytokine IL-1 in the development of atherosclerosis. Recent studies have provided direct evidence supporting a link between innate immunity and atherogenesis. Although it is still controversial about whether infectious pathogens contribute to cardiovascular diseases, direct genetic evidence indicates the importance of IL-1R/TLR signaling in atherogenesis. In this study, we examined the role of IL-1R-associated kinase 4 (IRAK4) kinase activity in modified low-density lipoprotein (LDL)-mediated signaling using bone marrow-derived macrophage as well as an in vivo model of atherosclerosis. First, we found that the IRAK4 kinase activity was required for modified LDL-induced NF-κB activation and expression of a subset of proinflammatory genes but not for the activation of MAPKs in bone marrow-derived macrophage. IRAK4 kinase-inactive knockin (IRAK4KI) mice were bred onto ApoE(-/-) mice to generate IRAK4KI/ApoE(-/-) mice. Importantly, the aortic sinus lesion formation was impaired in IRAK4KI/ApoE(-/-) mice compared with that in ApoE(-/-) mice. Furthermore, proinflammatory cytokine production was reduced in the aortic sinus region of IRAK4KI/ApoE(-/-) mice compared with that in ApoE(-/-) mice. Taken together, our results indicate that the IRAK4 kinase plays an important role in modified LDL-mediated signaling and the development of atherosclerosis, suggesting that pharmacological inhibition of IRAK4 kinase activity might be a feasible approach in the development of antiatherosclerosis drugs.


Asunto(s)
Aterosclerosis/enzimología , Aterosclerosis/inmunología , Regulación de la Expresión Génica/inmunología , Mediadores de Inflamación/administración & dosificación , Quinasas Asociadas a Receptores de Interleucina-1/fisiología , Lipoproteínas LDL/administración & dosificación , FN-kappa B/metabolismo , Acetilación , Animales , Aorta Torácica/enzimología , Aorta Torácica/metabolismo , Aorta Torácica/patología , Apolipoproteínas E/deficiencia , Apolipoproteínas E/genética , Aterosclerosis/patología , LDL-Colesterol/metabolismo , LDL-Colesterol/fisiología , Regulación de la Expresión Génica/genética , Inflamación/enzimología , Inflamación/genética , Inflamación/patología , Mediadores de Inflamación/metabolismo , Quinasas Asociadas a Receptores de Interleucina-1/antagonistas & inhibidores , Quinasas Asociadas a Receptores de Interleucina-1/deficiencia , Lipoproteínas LDL/metabolismo , Lipoproteínas LDL/fisiología , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , FN-kappa B/fisiología
3.
Allergy Rhinol (Providence) ; 5(2): 113-5, 2014 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-24988176

RESUMEN

We present a case report of a 5-year-old boy with presumed anaphylaxis to the caterpillar, Lophocampa maculata, manifesting as the acute development of diffuse urticaria and progressive dyspnea. This reaction required prompt treatment with antihistamines and a bronchodilator. Allergen scratch testing with a homogenized caterpillar extract suggests that immunoglobulin E-mediated type I hypersensitivity as the pathophysiological mechanism responsible for the boy's anaphylaxis. This case report represents the first documented occurrence of an anaphylactic reaction to Lophocampa maculata and adds to the rare incidence of documented hypersensitivity to the order Lepidoptera.

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