1979
DOI: 10.1002/9780470122938.ch2
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Glycosidases—Properties and Application to the Study of Complex Carbohydrates and Cell Surfaces

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1981
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Cited by 14 publications
(4 citation statements)
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References 298 publications
(71 reference statements)
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“…The engagement of mixed glioma-microglia monolayer cultures should be the next observation of the involvement of Siglec checkpoint in cellular direct interactions. Moreover, previous studies have shown that the structure of membrane glycoconjugates is highly variable and depends on the phase of cell division [89,90]. The estimation and comparison of sialylation and related changes in Siglecs recognition may be interesting in the range of different cell cycle phases of tested glioma cells.…”
Section: Discussionmentioning
confidence: 99%
“…The engagement of mixed glioma-microglia monolayer cultures should be the next observation of the involvement of Siglec checkpoint in cellular direct interactions. Moreover, previous studies have shown that the structure of membrane glycoconjugates is highly variable and depends on the phase of cell division [89,90]. The estimation and comparison of sialylation and related changes in Siglecs recognition may be interesting in the range of different cell cycle phases of tested glioma cells.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, the most effective Dex concentration decreasing Olig2 expression—10 µM—corresponded to that revealed as the most arresting G 0 /G 1 phase in GL261 and SMA560 cells. It has been shown previously that the total content of several monosaccharides is at minimum, whereas the degree of sialylation is at maximum just before and during cell division glycotopes [ 38 ]. It is in agreement with our observation that reduced sialylation correspond to Dex-induced growth inhibition in immunogenic SMA560 cells.…”
Section: Discussionmentioning
confidence: 99%
“…The supernatant from centrifugation of the homogenate at 5000 rpm for 15 min was utilized as an enzyme source (ES). Levels of the hydrolytic and detoxification enzymes amylase [33], protease [34], invertase [35], lipase [36], acid phosphatase [37], glycosidase [38], trehalase [39], phospholipase A 2 [40], esterase [41], and lactate dehydrogenase [42] were quantified using standard procedures as described below.…”
Section: Enzyme Bioassaymentioning
confidence: 99%