RESUMEN
DC-SIGN, a type II membrane protein with a C-type lectin binding domain that is highly expressed on mucosal dendritic cells (DCs) and certain macrophages in vivo, binds to ICAM-3, ICAM-2, and human and simian immunodeficiency viruses (HIV and SIV). Virus captured by DC-SIGN can be presented to T cells, resulting in efficient virus infection, perhaps representing a mechanism by which virus can be ferried via normal DC trafficking from mucosal tissues to lymphoid organs in vivo. To develop reagents needed to characterize the expression and in vivo functions of DC-SIGN, we cloned, expressed, and analyzed rhesus macaque, pigtailed macaque, and murine DC-SIGN and made a panel of monoclonal antibodies (MAbs) to human DC-SIGN. Rhesus and pigtailed macaque DC-SIGN proteins were highly similar to human DC-SIGN and bound and transmitted HIV type 1 (HIV-1), HIV-2, and SIV to receptor-positive cells. In contrast, while competent to bind virus, murine DC-SIGN did not transmit virus to receptor-positive cells under the conditions tested. Thus, mere binding of virus to a C-type lectin does not necessarily mean that transmission will occur. The murine and macaque DC-SIGN molecules all bound ICAM-3. We mapped the determinants recognized by a panel of 16 MAbs to the repeat region, the lectin binding domain, and the extreme C terminus of DC-SIGN. One MAb was specific for DC-SIGN, failing to cross-react with DC-SIGNR. Most MAbs cross-reacted with rhesus and pigtailed macaque DC-SIGN, although none recognized murine DC-SIGN. Fifteen of the MAbs recognized DC-SIGN on DCs, with MAbs to the repeat region generally reacting most strongly. We conclude that rhesus and pigtailed macaque DC-SIGN proteins are structurally and functionally similar to human DC-SIGN and that the reagents that we have developed will make it possible to study the expression and function of this molecule in vivo.
Asunto(s)
Moléculas de Adhesión Celular , Lectinas Tipo C , Lectinas/fisiología , Receptores de Superficie Celular/fisiología , Secuencia de Aminoácidos , Animales , Anticuerpos Monoclonales/inmunología , Mapeo Epitopo , Humanos , Lectinas/química , Lectinas/inmunología , Lectinas/metabolismo , Macaca mulatta , Macaca nemestrina , Ratones , Ratones Endogámicos BALB C , Datos de Secuencia Molecular , Conejos , Receptores de Superficie Celular/química , Receptores de Superficie Celular/inmunologíaRESUMEN
The C-type lectins DC-SIGN and DC-SIGNR capture and transfer human immunodeficiency virus (HIV) to susceptible cells, although the underlying mechanism is unclear. Here we show that DC-SIGN/DC-SIGNR-mediated HIV transmission involves dissociable binding and transfer steps, indicating that efficient virus transmission is not simply due to tethering of virus to the cell surface.
Asunto(s)
Moléculas de Adhesión Celular , Infecciones por VIH/transmisión , VIH/fisiología , Lectinas Tipo C , Lectinas/fisiología , Receptores de Superficie Celular/fisiología , Antígenos CD4/análisis , Proteína p24 del Núcleo del VIH/análisis , HumanosRESUMEN
Dendritic cells (DCs) efficiently bind and transmit human immunodeficiency virus (HIV) to cocultured T cells and so may play an important role in HIV transmission. DC-SIGN, a novel C-type lectin that is expressed in DCs, has recently been shown to bind R5 HIV type 1 (HIV-1) strains and a laboratory-adapted X4 strain. To characterize the interaction of DC-SIGN with primate lentiviruses, we investigated the structural determinants of DC-SIGN required for virus binding and transmission to permissive cells. We constructed a panel of DC-SIGN mutants and established conditions which allowed comparable cell surface expression of all mutants. We found that R5, X4, and R5X4 HIV-1 isolates as well as simian immunodeficiency and HIV-2 strains bound to DC-SIGN and could be transmitted to CD4/coreceptor-positive cell types. DC-SIGN contains a single N-linked carbohydrate chain that is important for efficient cell surface expression but is not required for DC-SIGN-mediated virus binding and transmission. In contrast, C-terminal deletions removing either the lectin binding domain or the repeat region abrogated DC-SIGN function. Trypsin-EDTA treatment inhibited DC-SIGN mediated infection, indicating that virus was maintained at the surface of the DC-SIGN-expressing cells used in this study. Finally, quantitative fluorescence-activated cell sorting analysis of AU1-tagged DC-SIGN revealed that the efficiency of virus transmission was strongly affected by variations in DC-SIGN expression levels. Thus, variations in DC-SIGN expression levels on DCs could greatly affect the susceptibility of human individuals to HIV infection.
Asunto(s)
Moléculas de Adhesión Celular , VIH-1/metabolismo , VIH-2/metabolismo , Lectinas Tipo C , Lectinas/metabolismo , Receptores de Superficie Celular/metabolismo , Receptores Virales/metabolismo , Virus de la Inmunodeficiencia de los Simios/metabolismo , Secuencia de Aminoácidos , Animales , Línea Celular Transformada , Membrana Celular/metabolismo , Ácido Edético , Expresión Génica , Glicosilación , Humanos , Lectinas/genética , Datos de Secuencia Molecular , Mutagénesis , Receptores de Superficie Celular/genética , Receptores Virales/genética , TripsinaRESUMEN
DC-SIGN, a C-type lectin expressed on the surface of dendritic cells (DCs), efficiently binds and transmits HIVs and simian immunodeficiency viruses to susceptible cells in trans. A DC-SIGN homologue, termed DC-SIGNR, has recently been described. Herein we show that DC-SIGNR, like DC-SIGN, can bind to multiple strains of HIV-1, HIV-2, and simian immunodeficiency virus and transmit these viruses to both T cell lines and human peripheral blood mononuclear cells. Binding of virus to DC-SIGNR was dependent on carbohydrate recognition. Immunostaining with a DC-SIGNR-specific antiserum showed that DC-SIGNR was expressed on sinusoidal endothelial cells in the liver and on endothelial cells in lymph node sinuses and placental villi. The presence of this efficient virus attachment factor on multiple endothelial cell types indicates that DC-SIGNR could play a role in the vertical transmission of primate lentiviruses, in the enabling of HIV to traverse the capillary endothelium in some organs, and in the presentation of virus to CD4-positive cells in multiple locations including lymph nodes.
Asunto(s)
Moléculas de Adhesión Celular , Endotelio/metabolismo , VIH-1/metabolismo , VIH-2/metabolismo , Lectinas Tipo C , Lectinas/metabolismo , Receptores de Superficie Celular/metabolismo , Virus de la Inmunodeficiencia de los Simios/metabolismo , Secuencia de Aminoácidos , Sitios de Unión , Línea Celular , Endotelio/citología , Humanos , Lectinas/genética , Hígado/citología , Hígado/metabolismo , Hígado/virología , Ganglios Linfáticos/citología , Ganglios Linfáticos/metabolismo , Ganglios Linfáticos/virología , Datos de Secuencia Molecular , Monocitos/virología , Placenta/citología , Placenta/metabolismo , Placenta/virología , Unión Proteica , Receptores de Superficie Celular/genética , Linfocitos T/virologíaRESUMEN
The amyloidogenic Abeta peptide is liberated from the amyloid precursor protein (APP) by two proteolytic activities, beta-secretase and gamma-secretase. Recently, a type I membrane protein termed BACE (beta-site APP cleaving enzyme) with characteristics of an aspartyl protease has been identified as the beta-secretase. We undertook a series of biochemical and morphological investigations designed to characterize the basic properties of this protein. Initial studies indicated that BACE undergoes N-linked glycosylation at three of four potential sites. Metabolic pulse-chase experiments revealed that after core glycosylation, BACE is rapidly and efficiently transported to the Golgi apparatus and distal secretory pathway. BACE was also found to be quite stable, being turned over with a t(12) of approximately 16 h. Retention of BACE in the endoplasmic reticulum by introduction of a C-terminal dilysine motif prevented complex carbohydrate processing and demonstrated that propeptide cleavage occurs after exit from this organelle. BACE exhibited intramolecular disulfide bonding but did not form oligomeric structures by standard SDS-polyacrylamide gel electrophoresis analysis and sedimented as a monomer in sucrose velocity gradients. Immunofluorescence studies showed a largely vesicular staining pattern for BACE that colocalized well with endosomal, but not lysosomal, markers. Measurable levels of BACE were also detected on the plasma membrane by both immunostaining and cell surface biotinylation, and cycling of the protein between the cell membrane and the endosomes was documented. A cytoplasmic dileucine motif was found to be necessary for normal targeting of BACE to the endosomal system and accumulation of the protein in this intracellular site.
Asunto(s)
Ácido Aspártico Endopeptidasas/química , Endosomas/metabolismo , Secuencias de Aminoácidos , Secuencia de Aminoácidos , Secretasas de la Proteína Precursora del Amiloide , Animales , Ácido Aspártico Endopeptidasas/metabolismo , Transporte Biológico , Disulfuros/química , Endocitosis , Endopeptidasas , Glicosilación , Lisosomas/enzimología , Datos de Secuencia Molecular , ConejosRESUMEN
Congenital antithrombin III (ATIII) deficiency, although uncommon, is a condition of considerable surgical importance. Affected patients are at significant risk of venous thrombosis during a surgical illness and standard forms of prophylaxis may not be effective. In addition, sequelae of their thromboses may in turn make them a candidate for venous surgery. An ATIII concentrate is now available in Australia for clinical use. This report describes two patients who underwent surgery for postphlebitic limbs utilizing infusions of ATIII concentrate. The ATIII deficiency state is reviewed and a method is described that should allow safe surgery in these patients.
Asunto(s)
Deficiencia de Antitrombina III , Tromboflebitis/cirugía , Adulto , Femenino , Humanos , Persona de Mediana Edad , Venas/cirugíaRESUMEN
Dissecting aneurysms of peripheral arteries within the extremities are very rare. We report a case of dissection of the superficial femoral and popliteal arteries, in which the preoperative arteriography was diagnostic and surgical treatment was undertaken before the onset of severe ischaemia. It is recommended that the diagnosis of dissecting aneurysm of a major artery should be considered when limb ischaemia occurs in a younger patient.
Asunto(s)
Disección Aórtica/diagnóstico , Arteria Femoral , Arteria Poplítea , Adulto , Disección Aórtica/complicaciones , Disección Aórtica/cirugía , Arteria Femoral/diagnóstico por imagen , Humanos , Claudicación Intermitente/etiología , Masculino , Arteria Poplítea/diagnóstico por imagen , RadiografíaRESUMEN
A case is reported of spontaneous perforation of the common hepatic duct in a patient presenting with a six-day history of painless jaundice and a one-day history of nausea and vomiting. An endoscopic retrograde cannulation of the common bile duct revealed a large stone in the distal end of the grossly dilated biliary tree. At operation a large collection of bile, sealed off by omentum, was found beneath the liver. A perforation was present in the common hepatic duct close to its junction with the cystic duct.