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Stimulation of collagen synthesis by insulin and proteoglycan accumulation by ascorbate in bovine keratocytes in vitro.

Stimulation of collagen synthesis by insulin and proteoglycan accumulation by ascorbate in bovine keratocytes in vitro. Research Abstract Details 

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  • Stimulation of collagen synthesis by insulin and proteoglycan accumulation by ascorbate in bovine keratocytes in vitro. Abstract Text:

    kurt musselmannKurt Musselmann,bradley kaneBradley Kane,bridgette alexandrouBridgette Alexandrou,john r hassellJohn R Hassell,

    PURPOSE: Ascorbate is required for the hydroxylation of collagen that is present in the corneal stroma. The keratan sulfate proteoglycans (KSPGs) lumican and keratocan are also present, and they interact with collagen and modulate its assembly into fibrils. In this study, ascorbate was added to a defined medium containing insulin, and its effects on the synthesis of collagen and KSPGs by keratocytes were determined. METHODS: Collagenase-isolated keratocytes were cultured with or without insulin with or without ascorbate. Collagen and glycosaminoglycan synthesis was determined by collagenase digestion of incorporated 3H-glycine and by chondroitinase ABC or endo-beta-galactosidase digestion of incorporated 35SO4. KSPGs were detected by Western blot. Collagen stability was determined by pepsin digestion. Ethyl-3,4-dihydroxybenzoate (EDB) was used to inhibit collagen hydroxylation. RESULTS: Insulin stimulated the synthesis of collagen but did not affect the accumulation of lumican and keratocan. Insulin plus ascorbate, however, stimulated the synthesis of collagen and increased the accumulation of these proteoglycans. The accumulation of PGDS, a KSPG that does not interact with collagen, was not affected by ascorbate. Only the collagen synthesized in the presence of ascorbate was pepsin resistant. EDB overrode the effects of ascorbate on pepsin resistance and proteoglycan accumulation. CONCLUSIONS: The results of this study indicate that the accumulation of lumican and keratocan depends in part on the level of collagen synthesis and its hydroxylation. The interaction of lumican and keratocan with the stably folded triple helix provided by hydroxylation may also serve to stabilize these proteoglycans.

    Stimulation of collagen synthesis by insulin and proteoglycan accumulation by ascorbate in bovine keratocytes in vitro. Publishing Authors By Initials

    k musselmannK Musselmann,b kaneB Kane,b alexandrouB Alexandrou,jr hassellJR Hassell,

    For similar carbohydrates: polysaccharides: proteoglycans research abstracts see: carbohydrates: polysaccharides: proteoglycans research

    PUBMED ID PMID:

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    Stimulation of collagen synthesis by insulin and proteoglycan accumulation by ascorbate in bovine keratocytes in vitro. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Investigative ophthalmology & visual science

    VOLUME: 47

    Page Numbers: 5260-6

    Journal Abbreviation: Invest. Ophthalmol. Vis. Sci.

    ISSN: 0146-0404

    DAY: 3

    MONTH: Dec

    YEAR: 2006

    Stimulation of collagen synthesis by insulin and proteoglycan accumulation by ascorbate in bovine keratocytes in vitro. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7703701

    Stimulation of collagen synthesis by insulin and proteoglycan accumulation by ascorbate in bovine keratocytes in vitro. Keywords Mesh Terms:

    KEYWORDS: Proteoglycans

    MESH TERMS: biosynthesis

    Chemical & Substance for Abstract: Stimulation of collagen synthesis by insulin and proteoglycan accumulation by ascorbate in bovine keratocytes in vitro. Information

    Substance Name: Keratan Sulfate

    Registry Number: 9056-36-4

    Grant and Affiliation Information for Stimulation of collagen synthesis by insulin and proteoglycan accumulation by ascorbate in bovine keratocytes in vitro.

    AFFILIATION: Department of Molecular Medicine, College of Medicine, University of South Florida, Tampa, Florida 33612, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NEI

    GRANT: EY08104

    ACRONYM: EY

    MEDLINETA: Invest Ophthalmol Vis Sci

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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