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Selective modulation of scleral proteoglycan mRNA levels during minus lens compensation and recovery.

Selective modulation of scleral proteoglycan mRNA levels during minus lens compensation and recovery. Research Abstract Details 

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  • Selective modulation of scleral proteoglycan mRNA levels during minus lens compensation and recovery. Abstract Text:

    john thomas siegwartJohn Thomas Siegwart,christianne e strangChristianne E Strang,

    PURPOSE: To better characterize the role of proteoglycans in scleral tissue remodeling during the development of minus lens induced myopia and during recovery in tree shrews. METHODS: Competitive reverse-transcription polymerase chain reaction (RT-PCR) was used to quantify the scleral mRNA levels for aggrecan, decorin, biglycan, and lumican in a group of tree shrews following four days of monocular -5 D lens treatment (n=5) and in a group after two days of recovery after 11 days of -5 D lens wear (n=5). Values were compared with age-matched normal animals (n=5). Aggrecan was localized within the sclera using immunohistochemistry. RESULTS: Four days of -5 D lens wear produced axial (vitreous chamber) elongation and a myopic shift in the treated eyes. Two days of recovery produced significant refractive recovery. Aggrecan mRNA levels showed differential, bidirectional regulation. Levels in the treated eye sclera relative to the control eye were 30.8%+/-2.4% lower after four days of -5 D lens treatment and 51.4%+/-2.4% higher after two days of recovery. Decorin, biglycan, and lumican mRNA levels showed little differential regulation. However, biglycan and lumican along with aggrecan showed binocular regulation (treated and control eye mRNA levels significantly lower than normal eye mRNA levels after 4 days of -5D lens treatment). Immunohistochemical results showed that aggrecan is present in tree shrew sclera and that it is located primarily between the collagen lamella and near the fibroblasts. CONCLUSIONS: These data suggest that the expression of aggrecan is strongly differentially modulated in the sclera during experimentally induced myopia and recovery. The modulation of aggrecan in concert with previously described changes in type I collagen and hyaluronan may play a key functional role in modulating the ability of the lamellae to slip across one another. This may be manifested in the scleral creep rate, which in turn modulates axial elongation rate and refractive state.

    Selective modulation of scleral proteoglycan mRNA levels during minus lens compensation and recovery. Publishing Authors By Initials

    jt siegwartJT Siegwart,ce strangCE Strang,

    For similar animals: chordata: vertebrates: mammals: scandentia: tupaiidae research abstracts see: animals: chordata: vertebrates: mammals: scandentia: tupaiidae research

    PUBMED ID PMID:

    MEDLINE DATE:

    Selective modulation of scleral proteoglycan mRNA levels during minus lens compensation and recovery. Journal Published:

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

    Journal: Molecular vision

    VOLUME: 13

    Page Numbers: 1878-86

    Journal Abbreviation: Mol. Vis.

    ISSN: 1090-0535

    DAY: 4

    MONTH: 10

    YEAR: 2007

    Selective modulation of scleral proteoglycan mRNA levels during minus lens compensation and recovery. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9605351

    Selective modulation of scleral proteoglycan mRNA levels during minus lens compensation and recovery. Keywords Mesh Terms:

    KEYWORDS: Tupaiidae

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Selective modulation of scleral proteoglycan mRNA levels during minus lens compensation and recovery. Information

    Substance Name: Keratan Sulfate

    Registry Number: 9056-36-4

    Grant and Affiliation Information for Selective modulation of scleral proteoglycan mRNA levels during minus lens compensation and recovery.

    AFFILIATION: Department of Vision Sciences, School of Optometry, The University of Alabama at Birmingham, Birmingham, AL, USA. siegwart@uab.edu

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NEI

    GRANT: R01 EY07845

    ACRONYM: EY

    MEDLINETA: Mol Vis

    REFSOURCE:

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