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1.
Glycobiology ; 23(2): 155-68, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-23019154

RESUMO

Chondroitin sulfate (CS) chains regulate the development of the central nervous system in vertebrates and are linear polysaccharides consisting of variously sulfated repeating disaccharides, [-4GlcUAß1-3GalNAcß1-](n), where GlcUA and GalNAc represent D-glucuronic acid and N-acetyl-D-galactosamine, respectively. CS chains containing D-disaccharide units [GlcUA(2-O-sulfate)-GalNAc(6-O-sulfate)] are involved in the development of cerebellar Purkinje cells and neurite outgrowth-promoting activity through interaction with a neurotrophic factor, pleiotrophin, resulting in the regulation of signaling. In this study, to obtain further structural information on the CS chains containing d-disaccharide units involved in brain development, oligosaccharides containing D-units were isolated from a shark fin cartilage. Seven novel hexasaccharide sequences, ΔO-D-D, ΔA-D-D, ΔC-D-D, ΔE-A-D, ΔD-D-C, ΔE-D-D and ΔA-B-D, in addition to three previously reported sequences, ΔC-A-D, ΔC-D-C and ΔA-D-A, were isolated from a CS preparation of shark fin cartilage after exhaustive digestion with chondroitinase AC-I, which cannot act on the galactosaminidic linkages bound to D-units. The symbol Δ stands for a 4,5-unsaturated bond of uronic acids, whereas A, B, C, D, E and O represent [GlcUA-GalNAc(4-O-sulfate)], [GlcUA(2-O-sulfate)-GalNAc(4-O-sulfate)], [GlcUA-GalNAc(6-O-sulfate)], [GlcUA(2-O-sulfate)-GalNAc(6-O-sulfate)], [GlcUA-GalNAc(4-O-, 6-O-sulfate)] and [GlcUA-GalNAc], respectively. In binding studies using an anti-CS monoclonal antibody, MO-225, the epitopes of which are involved in cerebellar development in mammals, novel epitope structures, ΔA-D-A, ΔA-D-D and ΔA-B-D, were revealed. Hexasaccharides containing two consecutive D-units or a B-unit will be useful for the structural and functional analyses of CS chains particularly in the neuroglycobiological fields.


Assuntos
Nadadeiras de Animais , Sulfatos de Condroitina , Condroitinases e Condroitina Liases , Oligossacarídeos , Acetilgalactosamina/química , Acetilgalactosamina/metabolismo , Nadadeiras de Animais/química , Nadadeiras de Animais/metabolismo , Animais , Cartilagem/química , Cartilagem/imunologia , Cartilagem/metabolismo , Sulfatos de Condroitina/química , Sulfatos de Condroitina/isolamento & purificação , Sulfatos de Condroitina/metabolismo , Condroitinases e Condroitina Liases/química , Condroitinases e Condroitina Liases/isolamento & purificação , Condroitinases e Condroitina Liases/metabolismo , Epitopos/imunologia , Epitopos/metabolismo , Fatores de Crescimento Neural/química , Fatores de Crescimento Neural/imunologia , Fatores de Crescimento Neural/metabolismo , Oligossacarídeos/química , Oligossacarídeos/isolamento & purificação , Oligossacarídeos/metabolismo , Ligação Proteica/imunologia , Células de Purkinje/metabolismo , Células de Purkinje/fisiologia , Tubarões , Sulfatos/imunologia , Sulfatos/metabolismo , Ácidos Urônicos/imunologia , Ácidos Urônicos/metabolismo
2.
Artigo em Inglês | MEDLINE | ID: mdl-36669121

RESUMO

To estimate the daily intake of food additives by young children aged 1-6 years in Japan, an intake survey was conducted in 2018 using the market basket method for food additives, including twelve types of colourants, three kinds of preservatives, three kinds of sweeteners and two kinds of food manufacturing agents. A list of the daily consumption of processed foods was prepared based on a special survey (MHLW 2011) and used for the estimation. The results of the survey showed that the food additives with the highest daily intake were phosphorus compounds (phosphoric acid and its salts; 11.2 mg/kg bw/day, expressed as phosphorus), followed by propylene glycol (0.80 mg/kg bw/day). The daily intake of other food additives ranged from 0 to 0.20 mg/kg bw/day. The estimated daily intake of each food additives by young children was compared with the acceptable daily intake (ADI) or maximum tolerable daily intake (MTDI). The highest ratio of the estimated daily intake to ADI was 3.2% for propylene glycol, whereas the ratios of the estimated daily intake to ADI for colourants, preservatives and sweeteners ranged from 0 to 1.1% (benzoic acid). The ratio of the estimated daily intake to MTDI for phosphorus compounds was 16%.


Assuntos
Dieta , População do Leste Asiático , Aditivos Alimentares , Criança , Pré-Escolar , Humanos , Propilenoglicol , Edulcorantes , Lactente , Compostos de Fósforo
3.
J Biol Chem ; 285(33): 25613-23, 2010 Aug 13.
Artigo em Inglês | MEDLINE | ID: mdl-20538610

RESUMO

Membrane tubulation is generally associated with rearrangements of the cytoskeleton and other cytoplasmic factors. Little is known about the contribution of extracellular matrix components to this process. Here, we demonstrate an essential role of proteoglycans in the tubulation of the cnidarian nematocyst vesicle. The morphogenesis of this extrusive organelle takes place inside a giant post-Golgi vesicle, which topologically represents extracellular space. This process includes the formation of a complex collagenous capsule structure that elongates into a long tubule, which invaginates after its completion. We show that a non-sulfated chondroitin appears as a scaffold in early morphogenesis of all nematocyst types in Hydra and Nematostella. It accompanies the tubulation of the vesicle membrane forming a provisional tubule structure, which after invagination matures by collagen incorporation. Inhibition of chondroitin synthesis by beta-xylosides arrests nematocyst morphogenesis at different stages of tubule outgrowth resulting in retention of tubule material and a depletion of mature capsules in the tentacles of hydra. Our data suggest a conserved role of proteoglycans in the stabilization of a membrane protrusion as an essential step in organelle morphogenesis.


Assuntos
Condroitina/metabolismo , Cnidários/metabolismo , Membranas Intracelulares/metabolismo , Organelas/metabolismo , Animais , Cromatografia em Gel , Imunofluorescência , Glicosaminoglicanos/metabolismo , Hydra/metabolismo , Imuno-Histoquímica
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