RESUMEN
Oviductus ranae (O.ran.) has been widely used as a tonic and a traditional animal-based Chinese medicine. O.ran. extracts have been reported to have numerous biological activities, including activities that are often associated with mammalian glycosaminoglycans such as anti-inflammatory, antiosteoperotic, and anti-asthmatic. Glycosaminoglycans are complex linear polysaccharides ubiquitous in mammals that possess a wide range of biological activities. However, their presence and possible structural characteristics within O.ran. were previously unknown. In this study, glycosaminoglycans were isolated from O.ran. and their disaccharide compositions were analyzed by liquid chromatography-ion trap/time-of-flight mass spectrometry (LC-MS-ITTOF). Heparan sulfate (HS)/heparin (HP), chondroitin sulfate (CS)/dermatan sulfate (DS) and hyaluronic acid (HA) were detected in O.ran. with varied disaccharide compositions. HS species contain highly acetylated disaccharides, and have various structures in their constituent chains. CS/DS chains also possess a heterogeneous structure with different sulfation patterns and densities. This novel structural information could help clarify the possible involvement of these polysaccharides in the biological activities of O.ran..
Asunto(s)
Glicosaminoglicanos/análisis , Glicosaminoglicanos/química , Materia Medica/química , Sulfatos de Condroitina/análisis , Cromatografía Liquida , Dermatán Sulfato/análogos & derivados , Dermatán Sulfato/análisis , Disacáridos/análisis , Disacáridos/aislamiento & purificación , Glicosaminoglicanos/aislamiento & purificación , Heparina/análisis , Heparitina Sulfato/análisis , Espectrometría de Masas/métodos , Sensibilidad y EspecificidadRESUMEN
Colla corii asini (CCA) made from donkey-hide has been widely used as a health-care food and an ingredient of traditional Chinese medicine. Heparan sulfate (HS)/heparin is a structurally complex class of glycosaminoglycans (GAGs) that have been implicated in a wide range of biological activities. However, their presence within CCA, and their possible structural characteristics, were previously unknown. In this study, GAG fractions containing HS/heparin were isolated from CCA and their disaccharide compositions were analyzed by high sensitivity liquid chromatography-ion trap/time-of-flight mass spectrometry (LC-MS-ITTOF). This revealed that, in addition to the eight commonly seen HS disaccharides, the four rare N-unsubstituted disaccharides were also detected in significant quantities. The disaccharide compositions varied significantly between HS/heparin fractions indicating chains with differing domain structures. This novel structural information may lead to a better understanding of the biological activities (i.e. anticoagulation and antitumor action) of CCA.
Asunto(s)
Gelatina/química , Heparina/química , Heparitina Sulfato/química , Heparina/análisis , Heparitina Sulfato/análisis , Espectrometría de Masa por Ionización de ElectrosprayRESUMEN
Heparanase plays an important role in the degradation of the extracellular matrix. It is implicated in inflammation, tumor angiogenesis and metastasis. We have developed two high-throughput methods for measuring heparanase activity and screening potential inhibitors. The first method involves coating fibroblast growth factor (FGF) on microtiter plates and capturing fluorescein isothiocyanate (FITC)-labeled heparin sulfate (HS), which is used as a substrate for heparanase digestion. Labeled HS fragments are released into the medium and quantitated by fluorescence intensity measurement. We have implemented this assay method into a Zeiss uHTS system and screened compound libraries for heparanase inhibitors. The second method involves labeling HS with biotin followed by FITC to generate a dual-labeled HS. The labeled material is bound to streptavidin-coated plates and used as a substrate for heparanase digestion. Both methods are sensitive and easily applicable to robotic systems. In addition, we have labeled both HS and biotin-HS with Eu-chelate, a fluorophore that exhibits long decay fluorescence. Assays using Eu-labeled HS and Eu-labeled biotin-HS have been developed and show higher sensitivity than those using FITC-labeled material. Furthermore, assays using Eu-chelate HS (or biotin-HS) should eliminate the interference of fluorescence compounds.
Asunto(s)
Antiinflamatorios/aislamiento & purificación , Antineoplásicos/aislamiento & purificación , Evaluación Preclínica de Medicamentos/métodos , Glucuronidasa/metabolismo , Animales , Antiinflamatorios/farmacología , Antineoplásicos/farmacología , Biotina/metabolismo , Células CHO , Bovinos , Células Cultivadas , Clonación Molecular , Cricetinae , Escherichia coli/genética , Factores de Crecimiento de Fibroblastos/metabolismo , Fluoresceína-5-Isotiocianato , Expresión Génica , Glucuronidasa/análisis , Glucuronidasa/genética , Heparitina Sulfato/análisis , Heparitina Sulfato/metabolismo , Humanos , Riñón/enzimología , Coloración y Etiquetado , TritioRESUMEN
In the present paper immunocytochemical analysis at the fluorescence microscopical level has been performed of neural cell adhesion. molecule (NCAM) immunoreactivity in the adult rat tel- and diencephalon in order to further substantiate the highly selective neuronal localization of NCAM immunoreactivity, using an affinity purified rabbit antiserum recognizing homologous NCAM proteins from rat brain. Also, double immunolabelling experiments were performed with monoclonal antibodies specific for heparan sulfate related epitopes or gamma-aminobutyric acid (GABA) to establish in which cell populations a colocalization existed with immunoreactive heparan sulfate proteoglycans of GABA. Within the neocortex NCAM immunoreactivity was exclusively localized to the area of the cell membrane of soma and proximal dendrites of subsets of large pyramidal nerve cells of the layer 5 of the frontoparietal cortex. Within the dorsal hippocampus, the NCAM immunoreactivity was exclusively located to the cell surface area of the pyramidal cell bodies of area CA2. Two colour immunofluorescence procedures demonstrated a colocalization of NCAM and 3G10 but not 10E4 immunoreactivities in the cell surface area of many of the NCAM-positive nerve cell bodies of these two regions. Within the thalamus, strong NCAM immunoreactivity was exclusively demonstrated at all rostrocaudal levels of the reticular thalamic nucleus. The horizontal band of NCAM immunoreactivity was not continuous, but split up into patches of NCAM immunoreactivity within groups of nerve cell bodies. When analysing the number of cells per unitary square in the rostrocaudal direction, a significant increase of positive cells was found in the rostral and middle thirds versus the caudal third of the reticular thalamic nucleus. Many of the cell bodies with NCAM immunoreactivity in their cell surface are showed cytoplasmic GABA immunoreactivity. In the three regions shown to contain NCAM immunoreactivity, proteins of the NCAM type may play a special role for the maintenance of the synaptic structure. The findings also suggest that the sulfated proteoglycans and NCAM can interact in the regulation of cell-cell interaction via adhesion. In the reticular thalamic nucleus NCAM molecules may be part of a set of cell-adhesion molecules involved in a structural organization of the nucleus, which allows it to play a key role in relating cortical maps to thalamic maps.
Asunto(s)
Moléculas de Adhesión Celular Neuronal/inmunología , Diencéfalo/química , Heparitina Sulfato/inmunología , Neuronas/química , Proteoglicanos/inmunología , Telencéfalo/química , Animales , Especificidad de Anticuerpos , Moléculas de Adhesión Celular Neuronal/análisis , Lóbulo Frontal/química , Proteoglicanos de Heparán Sulfato , Heparitina Sulfato/análisis , Hipocampo/química , Hipotálamo/química , Masculino , Microscopía Confocal , Neuronas/citología , Lóbulo Parietal/química , Proteoglicanos/análisis , Conejos , Ratas , Ratas Sprague-Dawley , Organismos Libres de Patógenos Específicos , Núcleos Talámicos/química , Ácido gamma-Aminobutírico/análisis , Ácido gamma-Aminobutírico/inmunologíaRESUMEN
The presence of proteoglycans bearing galactosaminoglycan chains has been reported, but none has been identified previously in the matrix of the Engelbreth-Holm-Swarm tumor, which is a source of several basement membrane components. This tumor matrix contains perlecan, a large, low buoyant density heparan sulfate proteoglycan, widespread in many basement membranes and connective tissues. We now identify two distinct proteoglycan species from this tumor source, which are substituted with galactosaminoglycans and which show basement membrane localization by immunohistochemistry. One species is perlecan but, in addition to being present as a heparan sulfate proteoglycan, it is also present as a hybrid molecule, with dermatan sulfate chains. A minor population of perlecan apparently lacks heparan sulfate chains totally, and some of this is substituted with chondroitin sulfate. The second species is immunologically related to basement membrane-chondroitin sulfate proteoglycan (BM-CSPG) and bears chondroitin sulfate chains. No BM-CSPG was detectable which was substituted with heparan sulfate chains. A combination of immunological and molecular approaches, including cDNA cloning, showed that perlecan and BM-CSPG are distinct in core protein structure. Both are, however, basement membrane components, although there are tissue-specific differences in their distribution.
Asunto(s)
Membrana Basal/química , Proteoglicanos Tipo Condroitín Sulfato/análisis , Proteoglicanos de Heparán Sulfato , Heparitina Sulfato/análisis , Neoplasias Experimentales/química , Proteoglicanos/análisis , Animales , Anticuerpos , Anticuerpos Monoclonales , Western Blotting , Proteoglicanos Tipo Condroitín Sulfato/biosíntesis , Clonación Molecular , ADN Complementario , Técnica del Anticuerpo Fluorescente Indirecta , Heparitina Sulfato/biosíntesis , Humanos , Inmunohistoquímica , Corteza Renal/citología , Ratones , Proteoglicanos/biosíntesis , Conejos , Ratas , Proteínas Recombinantes de Fusión/biosíntesis , Piel/citologíaRESUMEN
Proteoglycans (PGs) and lung hyaluronan (HA) are important components of the lung matrix both during normal development and in response to injury. We combined morphologic and biochemical techniques to study changes in PG and HA in a developmental series of Macaca nemestrina lungs ranging from 62% gestation to 3 mo post-term (n = 16), in adult lungs (n = 6), and from prematurely delivered, mechanically ventilated monkeys with hyaline membrane disease (HMD) (n = 7). Three groups of cuprolinic blue-positive (CuB) precipitates, identified by size, location, and susceptibility to enzyme digestion were found in lungs from all animals. Immature alveolar interstitium is characterized by loosely woven collagen bundles and an abundance of large (100 to 200 nm) stained filaments representing chondroitin sulfate proteoglycans (CSPGs). As maturation proceeds, the interstitial matrix appears increasingly organized, with large collagen bundles associated with 20 nm CuB-stained deposits (dermatan sulfate proteoglycans, DSPGs), and fewer large CSPGs. Fetal alveolar basement membrane contains CuB-stained heparin sulfate proteoglycans (HSPGs) (10 nm) scattered throughout. Lung matrix from animals with HMD appeared to have a disruption of the collagen-DSPG relationship, in addition to an enrichment in large CSPG. Complementary biochemical analysis of lung PGs and HA was done. Minced lung parenchyma was cultured with [3H]-glucosamine and [35S]-sulfate for 24 h; PGs and HA were extracted and analyzed. While PG synthesis during development tended to be highest at 80% gestation, animals with HMD showed greatly increased synthesis, approximately 2.5-fold higher than comparable fetal animals. In the developmental series, [3H]-glucosamine incorporation into HA was maximal at term, falling abruptly thereafter. HMD animals, however, showed a 2.3-fold increase over controls in net HA synthesis. Extracted PGs were separated according to buoyant density by dissociative cesium chloride density gradient ultracentrifugation. Two peaks of 35S-labeled PGs were separated from each density gradient fraction by chromatography on Sepharose CL-4B. A large CSPG was the principal PG eluting in the voiding volume, while the second broad peak (K(av) = 0.42) contained a mixed population of CSPG, DSPG, and HSPGs, the proportions of which varied with age. Both ultrastructural and biochemical analyses indicate that production of a large, high buoyant density CSPG predominates in fetal lung tissue, and diminishes with developmental age. Synthesis of large CSPG is greatly increased in lung explants from prematurely delivered animals with HMD.(ABSTRACT TRUNCATED AT 400 WORDS)
Asunto(s)
Envejecimiento/fisiología , Desarrollo Embrionario y Fetal/fisiología , Enfermedad de la Membrana Hialina/metabolismo , Pulmón/embriología , Pulmón/crecimiento & desarrollo , Proteoglicanos/metabolismo , Animales , Autorradiografía , Membrana Basal/patología , Membrana Basal/fisiología , Proteoglicanos Tipo Condroitín Sulfato/análisis , Proteoglicanos Tipo Condroitín Sulfato/metabolismo , Glucosamina/metabolismo , Proteoglicanos de Heparán Sulfato , Heparitina Sulfato/análisis , Heparitina Sulfato/metabolismo , Humanos , Enfermedad de la Membrana Hialina/patología , Recién Nacido , Pulmón/patología , Macaca nemestrina , Microscopía Electrónica , Técnicas de Cultivo de Órganos , Proteoglicanos/análisis , Alveolos Pulmonares/metabolismo , Alveolos Pulmonares/patología , Alveolos Pulmonares/ultraestructura , Sulfatos/metabolismo , Radioisótopos de Azufre , TritioRESUMEN
We have previously proposed that polysialic acid (PSA), which is attached to NCAM on the cell surface, can serve to regulate a variety of cell-cell interactions. The present study provides evidence that hydrated PSA influences a sufficiently large volume at the cell surface to exert broad steric effects, and that the removal of PSA in fact causes a detectable change in intercellular space. Using F11 neuron/neuroblastoma hybrid cells as a model system, the measured density and size of PSA suggests that a substantial fraction of the space between two apposed cell surface membranes could be sterically influenced by the presence of PSA. Specific enzymatic removal of PSA, which is similar in magnitude to changes that occur in many tissues during normal development, caused about a 25% decrease in the distance between two apposed cells. By contrast, removal of both heparan sulfate and chondroitin sulfate from the cells had no effect on this parameter. It is proposed that such changes in membrane-membrane distance could serve to alter selectively the efficiency of encounter between complementary receptors on apposing cells, and explain at least in part the broad biological influences of PSA.
Asunto(s)
Moléculas de Adhesión Celular Neuronal/química , Espacio Extracelular/fisiología , Neuronas/citología , Polisacáridos/análisis , Ácidos Siálicos/análisis , Animales , Moléculas de Adhesión Celular Neuronal/análisis , Línea Celular , Sulfatos de Condroitina/análisis , Heparitina Sulfato/análisis , Luz , Neuronas/química , Polisacáridos/química , Dispersión de Radiación , Ácidos Siálicos/química , Células Tumorales CultivadasRESUMEN
We compared the effects of mild hypercholesterolemia and repeated endotoxin infusions on the biochemical composition of aortic intima and inner media of 24 piglets divided into 4 groups 5 days after weaning: controls on normal diet (group I); normal diet and endotoxin (group II); fat-supplemented diet (group III); and fat-supplemented diet and endotoxin (group IV). It was found that mild hypercholesterolemia increased the concentration of arterial esterified cholesterol and the relative amount of the fraction containing chondroitin sulphates A and C in total glycosaminoglycans. Endotoxin infusions partly prevented the increase of serum cholesterol caused by the fat-supplemented diet but had no independent effect on the arterial biochemical composition; nor did they affect the biochemical changes caused by hypercholesterolemia. When the results of all groups were combined, chondroitin sulphates A and C showed a significant positive correlation with the concentration of arterial esterified cholesterol and the percentage of linoleic acid in arterial cholesteryl esters. Serum total cholesterol did not correlate with arterial cholesterol fractions, but the ratio of high density lipoprotein-cholesterol to total serum cholesterol showed a negative association with arterial esterified cholesterol. The present findings indicate that (1) mild hypercholesterolemia is atherogenic in young piglets, and (2) changes in arterial glycosaminoglycan composition might be one of the earliest biochemical alterations in atherogenesis.
Asunto(s)
Aorta Torácica/análisis , Arteriosclerosis/metabolismo , Endotoxinas/farmacología , Glicosaminoglicanos/análisis , Hipercolesterolemia/metabolismo , Lípidos/análisis , Músculo Liso Vascular/análisis , Animales , Colesterol/análisis , Sulfatos de Condroitina/análisis , Dermatán Sulfato/análisis , Dieta Aterogénica , Heparitina Sulfato/análisis , Ácido Hialurónico/análisis , Hipercolesterolemia/fisiopatología , Fosfolípidos/análisis , Valores de Referencia , PorcinosAsunto(s)
Glicósido Hidrolasas/metabolismo , Polisacáridos/análisis , Conformación de Carbohidratos , Celulosa/análisis , Quitina/análogos & derivados , Quitina/análisis , Quitosano , Sulfatos de Condroitina/análisis , Dermatán Sulfato/análisis , Glucanos/análisis , Heparina/análisis , Heparitina Sulfato/análisis , Sulfato de Queratano/análisis , Pectinas/análisis , Peptidoglicano/análisisRESUMEN
Copper deficiency results in defective elastin and collagen maturation in most tissues. A close relationship also exists between these components and proteoglycans in connective tissue. In an effort to obtain information on the nature of proteoglycans in copper deficiency, the composition of glycosaminoglycans in lungs from copper-deficient (1 micrograms/g of diet) or -supplemented (25 micrograms/g diet) chicks was studied. The total glycosaminoglycan concentration in copper-deficient chick lungs did not differ from that in control chick lungs. However, variations in individual glycosaminoglycan concentrations between lungs from copper-deficient and -supplemented chicks were observed. Heparan sulfate and dermatan sulfate concentrations were lower in copper-deficient chick lungs than in controls. The glycosaminoglycans from lungs of copper-deficient chicks also had lower molecular weights than glycosaminoglycans from lungs of control birds.
Asunto(s)
Cobre/deficiencia , Glicosaminoglicanos/análisis , Pulmón/análisis , Animales , Pollos , Sulfatos de Condroitina/análisis , Cromatografía en Gel , Cobre/administración & dosificación , Dermatán Sulfato/análisis , Heparitina Sulfato/análisis , Ácido Hialurónico/análisis , Pulmón/patología , Masculino , Peso MolecularRESUMEN
An unusual heparan sulfate was isolated from lobsters (Homarus americanus). The polysaccharide has a composition and properties intermediate to heparin and the more common heparan sulfates. The sulfate and D-glucuronic acid content is high, while anticoagulant activity is low. The major repeating unit appears to consist of D-glucuronic acid and D-glucosamine N-O-disulfate. Some N-acetyl groups are present, the content of L-iduronic acid O-sulfate is low, and monosulfated or nonsulfated disaccharide-repeating units (very common in heparan sulfates) appear to be very rare. The data obtained again emphasize the heterogeneity of heparan sulfates and the need for adequate characterization when dealing with unusual or unexplored sources.