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WFRF:(Hascall V. C.)
 

Sökning: WFRF:(Hascall V. C.) > Formation of proteo...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003703naa a2200301 4500
001oai:lup.lub.lu.se:b5a07ed1-cf82-4b97-8c49-d5c79fe1cfc5
003SwePub
008160504s1983 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/b5a07ed1-cf82-4b97-8c49-d5c79fe1cfc52 URI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Lohmander, Stefanu Lund University,Lunds universitet,Ortopedi, Lund,Sektion III,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Lund OsteoArthritis Division - Nedbrytning av ledbrosk: en biologisk process som leder till artros,Forskargrupper vid Lunds universitet,Orthopaedics (Lund),Section III,Department of Clinical Sciences, Lund,Faculty of Medicine,Lund OsteoArthritis Division - Molecular marker research group,Lund University Research Groups4 aut0 (Swepub:lu)ort-slo
2451 0a Formation of proteoglycan aggregates in rat chondrosarcoma chondrocyte cultures treated with tunicamycin
264 1c 1983
300 a 7 s.
520 a Proteoglycan monomer and link protein isolated from the Swarm rat chondrosarcoma both contain glycosylamine-linked oligosaccharides. In monomer, these N-linked oligosaccharides are concentrated in a region of the protein core which interacts specifically with both hyaluronate and link protein to form proteoglycan aggregates present in the cartilage matrix. Chondrocyte cultures were treated with tunicamycin to inhibit synthesis of the N-linked oligosaccharides, and the ability of the deficient proteoglycan and link protein to form aggregates was studied. Cultures were pretreated with tunicamycin for 3 h and then labeled with either [3H]mannose, [3H]glucosamine, [3H]serine, or with [35S]sulfate for 6 h in the presence of tunicamycin. Formation of link protein-stabilized proteoglycan aggregates in the culture medium was inhibited by up to 40% when the cells were treated with 3 μg of tunicamycin/ml, a concentration which inhibited 3H incorporation with mannose as a precursor by about 90%, but by only 15% with glucosamine as a precursor. When exogenous proteoglycan aggregate was added to the culture medium, however, it was found that both endogenous monomer and link protein synthesized in the presence of tunicamycin were fully able to form link-stabilized aggregates. This suggests that glycosylamine-linked oligosaccharides on monomer and on link protein are not necessary for their specific interactions with hyaluronate and with each other. Further, although tunicamycin did not inhibit net synthesis of hyaluronate, transfer of hyaluronate from the cell layer to the culture medium was retarded. This phenomenon accounted for most if not all of the decrease in the amount of proteoglycan which formed aggregates in the medium of cultures treated with tunicamycin.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Cell- och molekylärbiologi0 (SwePub)301082 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Cell and Molecular Biology0 (SwePub)301082 hsv//eng
700a Fellini, S. A.u National Institutes of Health, United States4 aut
700a Kimura, J. H.u National Institutes of Health, United States4 aut
700a Stevens, R. L.u National Institutes of Health, United States4 aut
700a Hascall, V. C.u National Institutes of Health, United States4 aut
710a Ortopedi, Lundb Sektion III4 org
773t Journal of Biological Chemistryg 258:20, s. 12280-12286q 258:20<12280-12286x 0021-9258
8564 8u https://lup.lub.lu.se/record/b5a07ed1-cf82-4b97-8c49-d5c79fe1cfc5

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