نتایج جستجو برای: hexosaminidase activity

تعداد نتایج: 1134871  

Journal: :Arthritis Research & Therapy 2009
Mária Pásztói György Nagy Pál Géher Tamás Lakatos Kálmán Tóth Károly Wellinger Péter Pócza Bence György Marianna C Holub Ágnes Kittel Krisztina Pálóczy Mercédesz Mazán Péter Nyirkos András Falus Edit I Buzas

INTRODUCTION Similar to matrix metalloproteinases, glycosidases also play a major role in cartilage degradation. Carbohydrate cleavage products, generated by these latter enzymes, are released from degrading cartilage during arthritis. Some of the cleavage products (such as hyaluronate oligosaccharides) have been shown to bind to Toll-like receptors and provide endogenous danger signals, while ...

Journal: :Saudi medical journal 2003
P Mc Nair Flor Bataclan Anuradha Ganesh

andhoff disease (GM2 gangliosidosis) is much less common than Tay-Sachs disease. Both are autosomal recessive lysosomal storage disorders (GM gangliosidoses). But Sandhoff disease is caused by mutations of the gene encoding the beta sub-unit of hexosaminidase, on chromosome 5. In Tay-Sachs disease, the mutation is in the alpha sub-unit on chromosome 15.1 Since both hexosaminidase A and hexosami...

Journal: :The Journal of Cell Biology 1986
D W Riches P M Henson

Sub-microgram quantities of bacterial lipopolysaccharide (LPS) have been found to substantially reduce the intracellular catalytic activities of three representative lysosomal enzymes (namely, acid phosphatase, hexosaminidase, and beta-glucuronidase) in human monocyte-derived macrophages. This response was not associated with a concurrent increase in enzyme catalytic activity in the culture sup...

Journal: :The Journal of biological chemistry 1981
A R Robbins R Myerowitz R J Youle G J Murray D M Neville

The localization of acid hydrolases was examined in Chinese hamster ovary cells with defective mannose 6-phosphate receptors; these mutants had been shown to exhibit reduced uptake and altered binding of exogenously added acid hydrolase (Robbins, A. R., Myerowitz, R., Youle, R. J., Murray, G. J., and Neville, D. M., Jr. (1981) J. Biol. Chem. 256, 10618-10622). Cells were grown in the presence o...

2012
Atsuko SAKURAI Natsu YAMAGUCHI Kei SONOYAMA

We investigated Candida albicans-induced mast cell degranulation in vitro and in vivo. Cell wall fraction but not culture supernatant and cell membrane fraction prepared from hyphally grown C. albicans induced β-hexosaminidase release in RBL-2H3 cells. Cell wall mannan and soluble β-glucan fractions also induced β-hexosaminidase release. Histological examination of mouse forestomach showed that...

Journal: :Journal of clinical pathology 1976
M McCormack

Hexosaminidase, alpha-mannosidase, beta-galactosidase, beta-glucuronidase, and arylsulphatase A were measured inperitoneal and pleural effusions from patients with benign, malignant, and inflammatory disorders. Compared with the benign transudates, all enzyme activities were moderately elevated in malignant effusions and markedly elevated in inflammatory effusions. The assay of hexosaminidase a...

Journal: :Journal of Bioscience and Bioengineering 2021

In the previous study, pickle-derived Lactiplantibacillus plantarum 22A-3 (LP22A3) suppressed ear edema in passive cutaneous anaphylaxis by its oral administration. Moreover, LP22A3 treatment directly to RBL-2H3 cells shows no effect on β-hexosaminidase release from but inhibited using Caco-2/RBL-2H3 co-culture system stimulated with apical side. this administration of decreased total IgE and o...

2014
Lucilla Parnetti Davide Chiasserini Emanuele Persichetti Paolo Eusebi Shiji Varghese Mohammad M Qureshi Andrea Dardis Marta Deganuto Claudia De Carlo Anna Castrioto Chiara Balducci Silvia Paciotti Nicola Tambasco Bruno Bembi Laura Bonanni Marco Onofrj Aroldo Rossi Tommaso Beccari Omar El-Agnaf Paolo Calabresi

To assess the discriminating power of multiple cerebrospinal fluid (CSF) biomarkers for Parkinson's disease (PD), we measured several proteins playing an important role in the disease pathogenesis. The activities of β-glucocerebrosidase and other lysosomal enzymes, together with total and oligomeric α-synuclein, and total and phosphorylated tau, were thus assessed in CSF of 71 PD patients and c...

2017
Vykuntaraju K. Gowda Raghavendraswami Amoghimath Varun M. Srinivasan Maya Bhat

Sandhoff disease is a neurodegenerative disease caused due to deficiency of hexosaminidase (HEX) A and B. A 1-year-old male child presented with regression of milestones, exaggerated startle response, decreased vision, and seizures from 6 months of age. The child had coarse facies without hepatosplenomegaly. Serum levels of β hexosaminidase total (A + B) were low. Genetic testing for Sandhoff d...

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