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1.
J Biol Chem ; 281(11): 7205-13, 2006 Mar 17.
Artículo en Inglés | MEDLINE | ID: mdl-16410241

RESUMEN

Receptor activity-modifying proteins (RAMPs) enable calcitonin receptor-like receptor (CRLR) to function as a calcitonin gene-related peptide receptor (CRLR/RAMP1) or an adrenomedullin (AM) receptor (CRLR/RAMP2 or -3). Here we investigated the functions of the cytoplasmic C-terminal tails (C-tails) of human RAMP1, -2, and -3 (hRAMP1, -2, and -3) by cotransfecting their C-terminal deletion or progressive truncation mutants into HEK-293 cells stably expressing hCRLR. Deletion of the C-tail from hRAMP1 had little effect on the surface expression, function, or intracellular trafficking of the mutant heterodimers. By contrast, deletion of the C-tail from hRAMP2 disrupted transport of hCRLR to the cell surface, resulting in significant reductions in (125)I-hAM binding and evoked cAMP accumulation. The transfection efficiency for the hRAMP2 mutant was comparable with that for wild-type hRAMP2; moreover, immunocytochemical analysis showed that the mutant hRAMP2 remained within the endoplasmic reticulum. FACS analysis revealed that deleting the C-tail from hRAMP3 markedly enhances AM-evoked internalization of the mutant heterodimers, although there was no change in agonist affinity. Truncating the C-tails by removing the six C-terminal amino acids of hRAMP2 and -3 or exchanging their C-tails with one another had no effect on surface expression, agonist affinity, or internalization of hCRLR, which suggests that the highly conserved Ser-Lys sequence within hRAMP C-tails is involved in cellular trafficking of the two AM receptors. Notably, deleting the respective C-tails from hRAMPs had no effect on lysosomal sorting of hCRLR. Thus, the respective C-tails of hRAMP2 and -3 differentially affect hCRLR surface delivery and internalization.


Asunto(s)
Péptido Relacionado con Gen de Calcitonina/química , Citoplasma/metabolismo , Receptores de Péptidos/química , Secuencia de Aminoácidos , Western Blotting , Línea Celular , Membrana Celular/metabolismo , Proliferación Celular , Separación Celular , AMP Cíclico/metabolismo , Cicloheximida/farmacología , ADN/química , ADN Complementario/metabolismo , Dimerización , Relación Dosis-Respuesta a Droga , Retículo Endoplásmico/metabolismo , Citometría de Flujo , Eliminación de Gen , Proteínas Fluorescentes Verdes/química , Humanos , Inmunohistoquímica , Péptidos y Proteínas de Señalización Intracelular/química , Péptidos y Proteínas de Señalización Intracelular/metabolismo , Lisina/química , Lisosomas/química , Lisosomas/metabolismo , Proteínas de la Membrana/química , Proteínas de la Membrana/metabolismo , Microscopía Fluorescente , Datos de Secuencia Molecular , Mutación , Unión Proteica , Estructura Terciaria de Proteína , ARN Mensajero/metabolismo , Proteína 1 Modificadora de la Actividad de Receptores , Proteína 2 Modificadora de la Actividad de Receptores , Proteínas Modificadoras de la Actividad de Receptores , Receptores de Adrenomedulina , Proteínas Recombinantes de Fusión/química , Serina/química , Factores de Tiempo , Transfección
2.
Circulation ; 110(4): 426-31, 2004 Jul 27.
Artículo en Inglés | MEDLINE | ID: mdl-15262849

RESUMEN

BACKGROUND: Adrenomedullin (AM) is expressed in cardiac tissue, and plasma AM levels increase in patients with acute myocardial infarction (MI). This study was performed to determine whether AM administration immediately after acute MI inhibits progression of heart failure in rats. METHODS AND RESULTS: Rats were infused with 1.0 microg/h IP AM or saline over 7 days immediately after MI inducted by left coronary ligation and were examined 9 weeks after MI. Compared with the saline infusion, AM infusion significantly improved survival (59% versus 81%; P<0.05) and body weight gain (32%; P<0.01) and reduced heart weight (-28%; P<0.01), lung weight (-26%; P<0.01), left ventricular (LV) end-diastolic pressure (11.4+/-2.0 versus 4.0+/-0.6 mm Hg, mean+/- SEM; P<0.01), collagen volume fraction of noninfarcted LV (-39%; P<0.05), and plasma levels of endogenous rat AM (-38%; P<0.05) without affecting infarct size. To investigate the mechanism of AM actions, another series of MI rats infused with AM were killed on day 7. AM infusion had no effect on organ weights and hemodynamic parameters on day 7 of MI but significantly reduced urinary excretion of isoprostane (-61%; P<0.01) and noninfarcted LV mRNA levels of ACE (-31%; P<0.05) and p22-phox (-30%; P<0.05). CONCLUSIONS: AM administration during the early period of MI improved the survival and ameliorated progression of LV remodeling and heart failure. This beneficial effect was accompanied by reductions in oxidative stress and ACE mRNA expression in noninfarcted LV in the AM infusion period.


Asunto(s)
Dinoprost/análogos & derivados , Insuficiencia Cardíaca/prevención & control , Infarto del Miocardio/tratamiento farmacológico , Péptidos/uso terapéutico , Adrenomedulina , Aldosterona/sangre , Animales , Peso Corporal/efectos de los fármacos , Dinoprost/orina , Progresión de la Enfermedad , Evaluación Preclínica de Medicamentos , Insuficiencia Cardíaca/etiología , Hemodinámica/efectos de los fármacos , Ligadura , Pulmón/efectos de los fármacos , Pulmón/patología , Masculino , Proteínas de Transporte de Membrana/biosíntesis , Proteínas de Transporte de Membrana/genética , Modelos Animales , Infarto del Miocardio/complicaciones , Infarto del Miocardio/metabolismo , Infarto del Miocardio/patología , Miocardio/patología , NADPH Deshidrogenasa/biosíntesis , NADPH Deshidrogenasa/genética , NADPH Oxidasas , Tamaño de los Órganos/efectos de los fármacos , Péptidos/administración & dosificación , Peptidil-Dipeptidasa A/biosíntesis , Peptidil-Dipeptidasa A/genética , Fosfoproteínas/biosíntesis , Fosfoproteínas/genética , ARN Mensajero/biosíntesis , Ratas , Ratas Wistar , Receptor de Angiotensina Tipo 1/biosíntesis , Receptor de Angiotensina Tipo 1/genética , Sistema Renina-Angiotensina/efectos de los fármacos , Remodelación Ventricular/efectos de los fármacos
3.
Circ J ; 67(8): 691-6, 2003 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-12890912

RESUMEN

The echocardiographic measures and plasma concentrations of either atrial natriuretic peptide (ANP) or brain natriuretic peptide (BNP) were compared in elite judo practitioners (static athletes), elite marathon runners (dynamic athletes) and healthy controls to investigate the relationship between the different types of left ventricular (LV) hypertrophy and plasma concentrations of natriuretic peptides in athletes. The LV mass and LV wall thickness of marathon runners and judo practitioners were significantly greater than those of controls. The LV end-diastolic dimension index was significantly larger in the marathon group, but smaller in the judo group. The left atrial dimension (LAD) index was significantly larger only in marathon runners. Plasma BNP concentrations were higher in both the judo and marathon groups than in controls, and positively correlated with LV mass as well as with deceleration time. Plasma ANP concentrations were significantly higher in marathon runners than in the controls and judo groups, and positively correlated with the LAD index, but negatively correlated with ejection fraction. Multivariate analyses showed that the type of athlete and LAD index were independent predictors of plasma BNP and ANP concentrations, respectively. Thus, there is an intimate link between plasma concentrations of natriuretic peptides and cardiac morphology in different types of athletes.


Asunto(s)
Factor Natriurético Atrial/sangre , Hipertrofia Ventricular Izquierda/sangre , Hipertrofia Ventricular Izquierda/etiología , Artes Marciales , Péptido Natriurético Encefálico/sangre , Carrera , Adulto , Ecocardiografía , Humanos , Hipertrofia Ventricular Izquierda/diagnóstico por imagen , Masculino , Análisis Multivariante , Concentración Osmolar , Volumen Sistólico
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