Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Más filtros

Banco de datos
Tipo del documento
Asunto de la revista
País de afiliación
Intervalo de año de publicación
1.
J Vasc Res ; 44(3): 241-8, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-17351328

RESUMEN

BACKGROUND: C-reactive protein (CRP) has been proven to facilitate endothelial injury via reduced NO production. Endothelial microparticles (EMPs) have emerged as a novel marker of endothelial injury. METHODS: In vitro cultured human umbilical vein endothelial cells (HUVECs) were incubated with CRP (20 mg/l) for 24 h. The numbers of EMPs with CD31- and CD51-positive staining were assessed flow-cytometrically, and NO production was measured using the Griess reaction in the presence or absence of tetrahydrobiopterin (BH(4)), respectively. RESULTS: The number of EMPs was significantly increased in HUVECs stimulated by CRP compared with the control group and, in parallel, NO production was decreased (p < 0.05). In the presence of CRP, pretreatment with BH(4) decreased EMP counts and restored NO production to baseline levels (p < 0.05) while pretreatment with 2,4-diamino-6-hydroxypyrimidine (DAHP), a BH(4) synthesis inhibitor, further prompted EMP formation and decreased NO production (p < 0.05). However, adding exogenous BH(4) after pretreatment with DAHP suppressed EMP formation and restored NO production (p < 0.05). CONCLUSIONS: This study demonstrates that CRP induces EMP generation in HUVECs and this effect is, at least in part, related to impaired BH(4)-dependent NO production. Augmented EMP generation in HUVECs is suggested as a novel potential mechanism contributing to the pathogenesis of vascular injury related to CRP.


Asunto(s)
Biopterinas/análogos & derivados , Proteína C-Reactiva/metabolismo , Células Endoteliales/metabolismo , Óxido Nítrico/metabolismo , Vesículas Transportadoras/metabolismo , Venas Umbilicales/metabolismo , Biopterinas/metabolismo , Biopterinas/farmacología , Proteína C-Reactiva/farmacología , Forma de la Célula , Células Cultivadas , Células Endoteliales/citología , Células Endoteliales/efectos de los fármacos , Inhibidores Enzimáticos/farmacología , GTP Ciclohidrolasa/antagonistas & inhibidores , GTP Ciclohidrolasa/metabolismo , Humanos , Hipoxantinas/farmacología , Fenotipo , Vesículas Transportadoras/efectos de los fármacos , Venas Umbilicales/citología , Venas Umbilicales/efectos de los fármacos
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA