1980
DOI: 10.1159/000172732
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Studies on the Catabolism of the Hydroxylysine-Linked Disaccharide Units of Basement Membranes and Collagens

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1983
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Cited by 9 publications
(14 citation statements)
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“…An age-dependent increase in ␤-galactosidase activity (at pH 6) has been reported (97), and a cell surface inactive ␤-galactosidase functions as an elastin and laminin receptor (98). An ␣-glucosidase that removes glucose from (Glc-Gal)Hyl has been characterized (99). However, we found no evidence that deglycosylation could be performed extracellularly, because triple-helical glycopeptides were not substrates for purified ␤-galactosidase or melanoma cells.…”
Section: Discussionmentioning
confidence: 62%
“…An age-dependent increase in ␤-galactosidase activity (at pH 6) has been reported (97), and a cell surface inactive ␤-galactosidase functions as an elastin and laminin receptor (98). An ␣-glucosidase that removes glucose from (Glc-Gal)Hyl has been characterized (99). However, we found no evidence that deglycosylation could be performed extracellularly, because triple-helical glycopeptides were not substrates for purified ␤-galactosidase or melanoma cells.…”
Section: Discussionmentioning
confidence: 62%
“…The complement, activated by the surgical procedure (Dvorak et al 1988), causes an increase in Clq, the degradation of which produces GGHyl (Krane et al 1977). In rats, GGHyl can in turn be transformed into GHyl by a kidney a-glucosidase (Sternberg & Spiro 1979). Indeed, the excretory patterns of GHyl and GGHyl are parallel, highly correlated and insensitive to the bone remodeling inhibition induced by estrogen administration, thus supporting the hypothesis that both glycosides are of extra-osseous origin.…”
Section: Discussionmentioning
confidence: 87%
“…The GHyl to GGHyl ratio varies depending on different tissues. In rats, bone contains higher levels of GGHyl than GHyl (Michalsky et al 1993) and a specific a-glucosidase in the kidney can convert the glucosyl fraction into the galactosyl one (Sternberg & Spiro 1979), so that both urinary GHyl and GGHyl should be measured when they are being used as indices of bone résorption. In contrast with pyridinium cross-links (Black et al 1989, Tordjman et al 1994, urinary glycosides have not yet been vali¬ dated as markers of increased bone résorption induced by estrogen deficiency.…”
Section: Introductionmentioning
confidence: 99%
“…In addition, there is the possibility that the decrease of both glycosides could be ascribed, at least in part, to clodronate inhibition of intracellular degradation of newly synthetised collagen (30) since GGHyl and GHyl might also derive from osteoblast synthetic activity and osteoblast intracellular degradation (3,29,31). Although rat bone contains more GGHyl than GHyl (32), the parallel changes of urinary glycosides are not unexpected since rat kidney cortex displays a specific a-glucosidase which converts the glucosyl fraction into the galactosyl form (33). However, we cannot exclude the possibilty that the reduction in urinary glycosides induced by clodronate might also be due to bisphosphonate effects on extraosseous sources of GGHyl e.g.…”
Section: Discussionmentioning
confidence: 99%