نتایج جستجو برای: heparan sulfate

تعداد نتایج: 59167  

Journal: :The Journal of Cell Biology 1980
Y S Kanwar A Linker M G Farquhar

Glomerular basement membranes (GBM's) were subjected to digestion in situ with glycosaminoglycan-degrading enzymes to assess the effect of removing glycosaminoglycans (GAG) on the permeability of the GBM to native ferritin (NF). Kidneys were digested by perfusion with enzyme solutions followed by perfusion with NF. In controls treated with buffer alone, NF was seen in high concentration in the ...

2014
Terrel Sugar Deborah J Wassenhove-McCarthy Jeffrey D Esko Toin H van Kuppevelt Lawrence Holzman Kevin J McCarthy

Heparan sulfate proteoglycans have been shown to modulate podocyte adhesion to--and pedicel organization on--the glomerular basement membrane. Recent studies showed that foot process effacement developed in a mutant mouse model whose podocytes were unable to assemble heparan sulfate glycosaminoglycan chains. This study, a further refinement, explored the role of heparan N-sulfation on podocyte ...

Journal: :The Journal of biological chemistry 2012
Regina Goetz Mutsuko Ohnishi Serkan Kir Hiroshi Kurosu Lei Wang Johanne Pastor Jinghong Ma Weiming Gai Makoto Kuro-o Mohammed S Razzaque Moosa Mohammadi

FGFs 19, 21, and 23 are hormones that regulate in a Klotho co-receptor-dependent fashion major metabolic processes such as glucose and lipid metabolism (FGF21) and phosphate and vitamin D homeostasis (FGF23). The role of heparan sulfate glycosaminoglycan in the formation of the cell surface signaling complex of endocrine FGFs has remained unclear. Here we show that heparan sulfate is not a comp...

Journal: :The Journal of Cell Biology 1976
R H Cohn J J Cassiman M R Bernfield

Mouse 3T3 cells and their Simian Virus 40-transformed derivatives (3T3SV) were used to assess the relationship of transfromation, cell density, and growth control to the cellular distribution of newly synthesized glycosaminoglycan (GAG). Glucosamine- and galactosamine-containing GAG were labeled equivalently by [3H=A1-glucose regardless of culture type, allowing incorporation into the various G...

2003
Enrique Brandan Juan Larrain

Heparan sulfate proteoglycans are key molecules found associated with the cell surface and extracellular matrix (ECM). These macromolecules seem to be essential to achieve terminal skeletal muscle differentiation. In this review, we present data about the types of beparan suifate proteoglycans present in skeletal muscle cells, how their expression changes during differentiation and we propose s...

Journal: :The Journal of Cell Biology 1983
J Laterra J E Silbert L A Culp

Proteins with affinities for specific glycosaminoglycans (GAC's) were used as probes for testing the potential of cell surface GAG's to mediate cell adhesive responses to extracellular matrices (ECM). Plasma fibronectin (FN) and proteins that bind hyaluronate (cartilage proteo-glycan core and link proteins) or heparan sulfate (platelet factor 4 [PF4]) were adsorbed to inert substrata to evaluat...

2014
Zhangguo Liu Fuming Zhang Lingyun Li Guoyun Li Wenqing He Robert J. Linhardt R. J. Linhardt

Glycosaminoglycans (GAGs) have numerous applications in the fields of pharmaceuticals, cosmetics, nutraceuticals, and foods. GAGs are also critically important in the developmental biology of all multicellular animals. GAGs were isolated from chicken egg components including yolk, thick egg white, thin egg white, membrane, calcified shell matrix supernatant, and shell matrix deposit. Disacchari...

Journal: :Journal of virology 1997
R K Williams S E Straus

Herpes simplex virus type 2 (HSV-2) interacts with cell surface glycosaminoglycans during virus attachment. Glycoprotein B of HSV-2 can potentially mediate the interaction between the virion and cell surface glycosaminoglycans. To determine the specificity, kinetics, and affinity of these interactions, we used plasmon resonance-based biosensor technology to measure HSV-2 glycoprotein binding to...

Journal: :The Journal of biological chemistry 1986
J A Marcum D H Atha L M Fritze P Nawroth D Stern R D Rosenberg

Cloned bovine aortic endothelial cells were cultured with [35S]Na2SO4 and proteolyzed extensively with papain. Radiolabeled heparan sulfate was isolated by DEAE-Sephacel chromatography. The mucopolysaccharide was then affinity fractionated into two separate populations utilizing immobilized antithrombin. The heparan sulfate, which bound tightly to the protease inhibitor, represented 0.84% of th...

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