Literature DB >> 11918305

The characterization of versican and its message in human articular cartilage and intervertebral disc.

Robert Sztrolovics1, Judy Grover, Gabriella Cs-Szabo, Shui-Liang Shi, Yiping Zhang, John S Mort, Peter J Roughley.   

Abstract

Splicing variation of the versican message and size heterogeneity of the versican core protein were analyzed in human articular cartilage and intervertebral disc. Splicing variation of the message was studied by PCR analysis to detect the presence or absence of exons 7 and 8, which encode large chondroitin sulfate attachment regions. At all ages in normal cartilage from the third trimester fetus to the mature adult, the presence of the versican isoform possessing exon 8 but not exon 7 (V1) could be readily detected. The message isoforms possessing neither exon 7 nor 8 (V3) or both exons 7 and 8 (V0) were only detectable in the fetus, and the isoform possessing only exon 7 (V2) was never detected. In osteoarthritic cartilage and in adult intervertebral disc the versican message pattern was the same as that observed in the normal adult with only the isoform possessing exon 8 being detected. Core protein heterogeneity was studied by immunoblotting following enzymic removal of the glycosaminoglycan chains from the proteoglycan, using an antibody recognizing the globular G1 region of versican. All articular cartilage extracts from the fetus to the mature adult contained multiple core protein sizes of greater than 200 kDa. The adult cartilage extracts tended to have an increased proportion of the smaller sized core proteins and osteoarthritic cartilage possessed similar core protein sizes to the normal adult. In contrast, intervertebral disc at all post-natal ages showed a greater range of size heterogeneity with a prominent component of about 50 kDa. The abundance of this component increased if the samples were treated with keratanase prior to analysis, suggesting that the G1 region of versican in disc can be substituted with keratan sulfate. The increased presence of versican in the disc relative to articular cartilage may suggest a more pronounced functional role for this proteoglycan, particularly in the nucleus pulposus.

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Year:  2002        PMID: 11918305     DOI: 10.1016/S0736-0266(01)00110-3

Source DB:  PubMed          Journal:  J Orthop Res        ISSN: 0736-0266            Impact factor:   3.494


  24 in total

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3.  The structure and degradation of aggrecan in human intervertebral disc.

Authors:  Peter J Roughley; Lee I Melching; Terrence F Heathfield; Richard H Pearce; John S Mort
Journal:  Eur Spine J       Date:  2006-05-31       Impact factor: 3.134

Review 4.  Cell and molecular biology of intervertebral disc degeneration: current understanding and implications for potential therapeutic strategies.

Authors:  S Z Wang; Y F Rui; J Lu; C Wang
Journal:  Cell Prolif       Date:  2014-08-11       Impact factor: 6.831

5.  Topographical variation in the distributions of versican, aggrecan and perlecan in the foetal human spine reflects their diverse functional roles in spinal development.

Authors:  Susan M Smith; John M Whitelock; Renato V Iozzo; Christopher B Little; James Melrose
Journal:  Histochem Cell Biol       Date:  2009-08-11       Impact factor: 4.304

Review 6.  Glycosaminoglycan synthesis in the nucleus pulposus: Dysregulation and the pathogenesis of disc degeneration.

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Journal:  Matrix Biol       Date:  2018-03-01       Impact factor: 11.583

7.  Comparison of age-dependent expression of aggrecan and ADAMTSs in mandibular condylar cartilage, tibial growth plate, and articular cartilage in rats.

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8.  Transcriptional profiling of bovine intervertebral disc cells: implications for identification of normal and degenerate human intervertebral disc cell phenotypes.

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9.  The effect of extracellular pH on matrix turnover by cells of the bovine nucleus pulposus.

Authors:  Sajjad Razaq; Robert J Wilkins; Jill P G Urban
Journal:  Eur Spine J       Date:  2003-07-16       Impact factor: 3.134

10.  Immunolocalization of proteoglycans in Meckel's cartilage of the rat.

Authors:  Khansa Taha Ababneh; Taiseer Hussain Al-Khateeb
Journal:  Open Dent J       Date:  2009-08-22
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