Matches in SemOpenAlex for { <https://semopenalex.org/work/W2058963737> ?p ?o ?g. }
- W2058963737 endingPage "728" @default.
- W2058963737 startingPage "722" @default.
- W2058963737 abstract "In Brief Study Design. This in vitro study used the alginate bead culture system to probe for differences in the effects of fibronectin fragment on cell proliferation and proteoglycan metabolism by different populations of intervertebral disc cells and articular chondrocytes. Objective. To compare the effects of fibronectin fragment on cell proliferation, and proteoglycan synthesis and degradation by cells from the nucleus pulposus, the anulus fibrosus, and articular cartilage. Summary of Background Data. In articular cartilage, the administration of fibronectin fragment stimulates cartilage degeneration. Fibronectin fragment levels were increased in human intervertebral discs with increased disc degeneration. Fibronectin fragment injected into the central region of the rabbit intervertebral disc induced a progressive degeneration of that disc. Methods. Bovine tails and metacarpophalangeal joints from 14- to 18-month-old animals were used. Alginate beads containing cells isolated from intervertebral discs and articular cartilage were cultured with (1–100 nmol/L) or without (control) fibronectin fragment in the presence of 10% fetal bovine serum. In these cultures, deoxyribonucleic acid and proteoglycan contents, as well as the rate of proteoglycan synthesis were determined. Proteoglycan degradation was measured in cultures with or without 10 nmol/L fibronectin fragment. Results. In articular chondrocytes, fibronectin fragment strongly suppressed proteoglycan synthesis and stimulated proteoglycan degradation; the total proteoglycan content was diminished in a dose-dependent manner. Compared to articular chondrocytes, nucleus pulposus cells responded to fibronectin fragments in a similar, although less pronounced manner. On the other hand, anulus fibrosus cells treated with fibronectin fragment did not show any significant effects on proteoglycan degradation. A slight but statistically significant up-regulation of proteoglycan synthesis was observed at 10 nmol/L fibronectin fragment in outer anulus fibrosus cells. However, total proteoglycan content was decreased significantly at high concentrations of fibronectin fragment. Conclusions. Fibronectin fragment has different effects on cell proliferation, proteoglycan synthesis, degradation, and accumulation by articular chondrocytes and intervertebral disc cells. The different effects of fibronectin fragment in those different cell types suggest metabolic differences between these cells, and may further suggest differences in pathways of fibronectin fragment signaling as well as a differential need of these cells to be involved in tissue remodeling in which both anabolic and catabolic pathways might be altered. The effects of fibronectin fragment on proteoglycan metabolism by intervertebral disc cells and articular chondrocytes were studied. Compared to articular chondrocytes, nucleus pulposus cells showed a similar but milder suppression of cell proliferation and proteoglycan synthesis, and increased proteoglycan degradation. Anulus fibrosus cells were unresponsive except at very high fibronectin fragment concentrations." @default.
- W2058963737 created "2016-06-24" @default.
- W2058963737 creator A5000662848 @default.
- W2058963737 creator A5012931115 @default.
- W2058963737 creator A5018901294 @default.
- W2058963737 creator A5025204726 @default.
- W2058963737 creator A5026974503 @default.
- W2058963737 creator A5031276487 @default.
- W2058963737 creator A5069437689 @default.
- W2058963737 date "2005-04-01" @default.
- W2058963737 modified "2023-10-01" @default.
- W2058963737 title "Differential Effects of Fibronectin Fragment on Proteoglycan Metabolism by Intervertebral Disc Cells: A Comparison With Articular Chondrocytes" @default.
- W2058963737 cites W1552444104 @default.
- W2058963737 cites W1617781531 @default.
- W2058963737 cites W1904364980 @default.
- W2058963737 cites W1967194093 @default.
- W2058963737 cites W1972026947 @default.
- W2058963737 cites W1980095106 @default.
- W2058963737 cites W1982985339 @default.
- W2058963737 cites W1983968835 @default.
- W2058963737 cites W1984594004 @default.
- W2058963737 cites W1994842854 @default.
- W2058963737 cites W2002201489 @default.
- W2058963737 cites W2002236075 @default.
- W2058963737 cites W2005165360 @default.
- W2058963737 cites W2006124822 @default.
- W2058963737 cites W2011353910 @default.
- W2058963737 cites W2017904233 @default.
- W2058963737 cites W2020291353 @default.
- W2058963737 cites W2023346148 @default.
- W2058963737 cites W2031897866 @default.
- W2058963737 cites W2035469813 @default.
- W2058963737 cites W2036264639 @default.
- W2058963737 cites W2045578437 @default.
- W2058963737 cites W2046753334 @default.
- W2058963737 cites W2058932182 @default.
- W2058963737 cites W2062823318 @default.
- W2058963737 cites W2066088112 @default.
- W2058963737 cites W2077009549 @default.
- W2058963737 cites W2087115556 @default.
- W2058963737 cites W2092071763 @default.
- W2058963737 cites W2134356637 @default.
- W2058963737 cites W2141968343 @default.
- W2058963737 cites W2187684329 @default.
- W2058963737 cites W2334161627 @default.
- W2058963737 cites W2336336714 @default.
- W2058963737 cites W4297924397 @default.
- W2058963737 doi "https://doi.org/10.1097/01.brs.0000157417.59933.db" @default.
- W2058963737 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15803072" @default.
- W2058963737 hasPublicationYear "2005" @default.
- W2058963737 type Work @default.
- W2058963737 sameAs 2058963737 @default.
- W2058963737 citedByCount "29" @default.
- W2058963737 countsByYear W20589637372012 @default.
- W2058963737 countsByYear W20589637372013 @default.
- W2058963737 countsByYear W20589637372014 @default.
- W2058963737 countsByYear W20589637372016 @default.
- W2058963737 countsByYear W20589637372017 @default.
- W2058963737 countsByYear W20589637372019 @default.
- W2058963737 countsByYear W20589637372021 @default.
- W2058963737 countsByYear W20589637372022 @default.
- W2058963737 countsByYear W20589637372023 @default.
- W2058963737 crossrefType "journal-article" @default.
- W2058963737 hasAuthorship W2058963737A5000662848 @default.
- W2058963737 hasAuthorship W2058963737A5012931115 @default.
- W2058963737 hasAuthorship W2058963737A5018901294 @default.
- W2058963737 hasAuthorship W2058963737A5025204726 @default.
- W2058963737 hasAuthorship W2058963737A5026974503 @default.
- W2058963737 hasAuthorship W2058963737A5031276487 @default.
- W2058963737 hasAuthorship W2058963737A5069437689 @default.
- W2058963737 hasConcept C105702510 @default.
- W2058963737 hasConcept C153911025 @default.
- W2058963737 hasConcept C189165786 @default.
- W2058963737 hasConcept C2777755357 @default.
- W2058963737 hasConcept C2779335624 @default.
- W2058963737 hasConcept C2780550940 @default.
- W2058963737 hasConcept C71924100 @default.
- W2058963737 hasConcept C86492073 @default.
- W2058963737 hasConcept C86803240 @default.
- W2058963737 hasConcept C95444343 @default.
- W2058963737 hasConceptScore W2058963737C105702510 @default.
- W2058963737 hasConceptScore W2058963737C153911025 @default.
- W2058963737 hasConceptScore W2058963737C189165786 @default.
- W2058963737 hasConceptScore W2058963737C2777755357 @default.
- W2058963737 hasConceptScore W2058963737C2779335624 @default.
- W2058963737 hasConceptScore W2058963737C2780550940 @default.
- W2058963737 hasConceptScore W2058963737C71924100 @default.
- W2058963737 hasConceptScore W2058963737C86492073 @default.
- W2058963737 hasConceptScore W2058963737C86803240 @default.
- W2058963737 hasConceptScore W2058963737C95444343 @default.
- W2058963737 hasIssue "7" @default.
- W2058963737 hasLocation W20589637371 @default.
- W2058963737 hasLocation W20589637372 @default.
- W2058963737 hasOpenAccess W2058963737 @default.
- W2058963737 hasPrimaryLocation W20589637371 @default.
- W2058963737 hasRelatedWork W1999210606 @default.
- W2058963737 hasRelatedWork W2021048391 @default.
- W2058963737 hasRelatedWork W2045578437 @default.