Topic
Keratan sulfate
About: Keratan sulfate is a research topic. Over the lifetime, 1253 publications have been published within this topic receiving 57984 citations. The topic is also known as: keratan sulfate & KS.
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TL;DR: The correlations of distinct glycoconjugate compositions with specific regeneration morphologies suggest the possibility that these components may be related to the phenotypic expression of tissues during regeneration.
Abstract: The present study identifies, localizes, and reports the relative composition of specific glycosaminoglycans within tissue matrices during the initiation phase of limb regeneration. The regenerate tissues were harvested and assayed morphologically, histochemically, and chemically. We observed 1) a population of cells interspersed among the cells of the dermis, epimysium, perimysium, perichondrium, and periosteum. 2) This population was distinguishable by a unique pattern of glycoconjugate staining, i.e., intracellular and pericellular heparan sulfate and glycoproteins and extracellularly associated hyaluronate and glycoproteins. 3) Cells with these staining characteristics aggregated to a position directly beneath the apical epidermal cap. 4) Extracellular hyaluronate and glycoproteins colocalized with undifferentiated tissues. And 5) extracellular chondroitin sulfate, dermatan sulfate, and keratan sulfate glycosaminoglycans colocalized with differentiated tissues. The correlations of distinct glycoconjugate compositions with specific regeneration morphologies suggest the possibility that these components may be related to the phenotypic expression of tissues during regeneration.
27 citations
TL;DR: It is suggested that biglycan and decorin are involved in the adaptation of articular cartilage to variations in loading regime.
Abstract: Sesamoid bone cartilage from the metacarpophalangeal joints of 5-year-old cows was cultured intact on its bone support. The incorporation of sulfate increased similarly in experimental cartilage that was subjected to cyclic loading (0.2 MPa, 0.2 Hz) for a week and in control cartilage that was cultured without loading. The synthesis of a population of small macromolecules decreased in the cultured controls, but was maintained at a constant level in the experimental samples. This population was isolated through Sepharose CL-2B chromatography. Subsequent application to Sepharose CL-4B yielded two distinct peaks. One contained protein-free chondroitin sulfate, keratan sulfate, and possibly some dermatan sulfate glycosaminoglycans. The other, more prominent, peak consisted of dermatan sulfate proteoglycans. This peak material was pooled, and applied to a 4-15% SDS-gel. The material was separated into two major bands, which represented biglycan and decorin. They decreased to less than half their day-0 value, in the cultured control. In the loaded cartilage, biglycan synthesis remained constant while decorin synthesis increased. These findings suggest that biglycan and decorin are involved in the adaptation of articular cartilage to variations in loading regime.
27 citations
TL;DR: Oligonucleotide primers which were designed based on identical peptide sequences flanking the interglobular domain (IGD) of human, bovine and rat aggrecan were used in RT-PCR reactions containing human, porcine, equine, bivine and ovine cartilage RNA, providing essential amino acid sequence data for species commonly used in model systems of cartilage degeneration.
27 citations
TL;DR: Study results suggest that carrageenan inhibition of sulfatase activity leads to re-distribution of the cellular GAG composition with increase in di-sulfated CS and with potential consequences for cell structure and function.
27 citations
TL;DR: Proteoglycans were extracted from normal and degenerate cartilage of the human tibial plateau and there was no evidence for the changes in glycosaminoglycan synthesis that have been described for clinically osteoarthritic cartilage, or for changes in the ability to aggregate with hyaluronic acid.
Abstract: Proteoglycans were extracted from normal and degenerate cartilage of the human tibial plateau. Both areas possessed proteoglycans of similar chemical composition, though the degenerate cartilage contained a greater proportion of molecules of lower buoyant density and enriched in keratan sulfate. There was no evidence for the changes in glycosaminoglycan synthesis that have been described for clinically osteoarthritic cartilage, or for changes in the ability to aggregate with hyaluronic acid.
26 citations