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Retinal Microglia and Uveal Tract Dendritic Cells and Macrophages Are Not CX3CR1 Dependent in Their Recruitment and Distribution in the Young Mouse Eye.

Retinal Microglia and Uveal Tract Dendritic Cells and Macrophages Are Not CX3CR1 Dependent in Their Recruitment and Distribution in the Young Mouse Eye. Research Abstract Details 

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  • Retinal Microglia and Uveal Tract Dendritic Cells and Macrophages Are Not CX3CR1 Dependent in Their Recruitment and Distribution in the Young Mouse Eye. Abstract Text:

    jelena kezicJelena Kezic,heping xuHeping Xu,holly r chinneryHolly R Chinnery,connor c murphyConnor C Murphy,paul g mcmenaminPaul G McMenamin,

    PURPOSE: The chemokine receptor CX3CR1 is expressed by monocyte-derived dendritic cells (DCs) and macrophages. CX3CR1 mediates leukocyte migration and adhesion in homeostatic and inflammatory conditions. Mice lacking Cx3cr1 have altered distribution and function of DC subpopulations in some tissue microenvironments. The present study compares the distribution of monocyte-derived cells in the normal retina and uveal tract as a prelude to the investigation of the role of CX3CR1 in murine models of ocular disease. METHODS: Transgenic mice in which either one (Cx3cr1(gfp/+), heterozygous) or both (Cx3cr1(gfp/gfp), homozygous) copies of the Cx3cr1 gene have been replaced by the enhanced green fluorescent protein (eGFP) reporter gene were used to investigate the role of Cx3cr1 expression on macrophages and DCs in the normal uveal tract and retina. Chimeric mice were used to investigate turnover of these cells in the normal, uninflamed eye. RESULTS: Confocal analysis found no significant differences in the density, phenotype or morphology of eGFP(+) cells between Cx3cr1(gfp/+) and Cx3cr1(gfp/+) mice in immunostained iris, ciliary body, or choroidal and retinal wholemounts. Flow cytometry also failed to detect any difference in the density or cell shape of eGFP(+) cells between Cx3cr1(gfp/+) and Cx3cr1(gfp/+) mice. Chimeras revealed 73% turnover of monocyte-derived cells in the iris and 63% in the choroid by 6 weeks after transplantation. CONCLUSIONS: These data illustrate that homing or migration of DCs and macrophages to the uveal tract and retina in normal young mice is not Cx3cr1 dependent and provide a solid foundation for future studies of monocyte-derived cells and the role of Cx3cr1 in models of ocular disease.

    Retinal Microglia and Uveal Tract Dendritic Cells and Macrophages Are Not CX3CR1 Dependent in Their Recruitment and Distribution in the Young Mouse Eye. Publishing Authors By Initials

    j kezicJ Kezic,h xuH Xu,hr chinneryHR Chinnery,cc murphyCC Murphy,pg mcmenaminPG McMenamin,

    For similar abstracts research abstracts see: abstracts research

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    Retinal Microglia and Uveal Tract Dendritic Cells and Macrophages Are Not CX3CR1 Dependent in Their Recruitment and Distribution in the Young Mouse Eye. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Investigative ophthalmology & visual science

    VOLUME: 49

    Page Numbers: 1599-608

    Journal Abbreviation:

    ISSN: 0146-0404

    DAY: 3

    MONTH: Apr

    YEAR: 2008

    Retinal Microglia and Uveal Tract Dendritic Cells and Macrophages Are Not CX3CR1 Dependent in Their Recruitment and Distribution in the Young Mouse Eye. Information

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    LANGUAGE: eng

    NlmUniqueID: 7703701

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    Grant and Affiliation Information for Retinal Microglia and Uveal Tract Dendritic Cells and Macrophages Are Not CX3CR1 Dependent in Their Recruitment and Distribution in the Young Mouse Eye.

    AFFILIATION: School of Anatomy and Human Biology, The University of Western Australia, Crawley, Western Australia; the.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Invest Ophthalmol Vis Sci

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