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      Gene Expression and Functional Annotation of the Human Ciliary Body Epithelia

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          Abstract

          Purpose

          The ciliary body (CB) of the human eye consists of the non-pigmented (NPE) and pigmented (PE) neuro-epithelia. We investigated the gene expression of NPE and PE, to shed light on the molecular mechanisms underlying the most important functions of the CB. We also developed molecular signatures for the NPE and PE and studied possible new clues for glaucoma.

          Methods

          We isolated NPE and PE cells from seven healthy human donor eyes using laser dissection microscopy. Next, we performed RNA isolation, amplification, labeling and hybridization against 44×k Agilent microarrays. For microarray conformations, we used a literature study, RT-PCRs, and immunohistochemical stainings. We analyzed the gene expression data with R and with the knowledge database Ingenuity.

          Results

          The gene expression profiles and functional annotations of the NPE and PE were highly similar. We found that the most important functionalities of the NPE and PE were related to developmental processes, neural nature of the tissue, endocrine and metabolic signaling, and immunological functions. In total 1576 genes differed statistically significantly between NPE and PE. From these genes, at least 3 were cell-specific for the NPE and 143 for the PE. Finally, we observed high expression in the (N)PE of 35 genes previously implicated in molecular mechanisms related to glaucoma.

          Conclusion

          Our gene expression analysis suggested that the NPE and PE of the CB were quite similar. Nonetheless, cell-type specific differences were found. The molecular machineries of the human NPE and PE are involved in a range of neuro-endocrinological, developmental and immunological functions, and perhaps glaucoma.

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          Most cited references132

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          Normalization of cDNA microarray data.

          Normalization means to adjust microarray data for effects which arise from variation in the technology rather than from biological differences between the RNA samples or between the printed probes. This paper describes normalization methods based on the fact that dye balance typically varies with spot intensity and with spatial position on the array. Print-tip loess normalization provides a well-tested general purpose normalization method which has given good results on a wide range of arrays. The method may be refined by using quality weights for individual spots. The method is best combined with diagnostic plots of the data which display the spatial and intensity trends. When diagnostic plots show that biases still remain in the data after normalization, further normalization steps such as plate-order normalization or scale-normalization between the arrays may be undertaken. Composite normalization may be used when control spots are available which are known to be not differentially expressed. Variations on loess normalization include global loess normalization and two-dimensional normalization. Detailed commands are given to implement the normalization techniques using freely available software.
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            Prevalence of open-angle glaucoma among adults in the United States.

            To estimate the prevalence and distribution of open-angle glaucoma (OAG) in the United States by age, race/ethnicity, and gender. Summary prevalence estimates of OAG were prepared separately for black, Hispanic, and white subjects in 5-year age intervals starting at 40 years. The estimated rates were based on a meta-analysis of recent population-based studies in the United States, Australia, and Europe. These rates were applied to 2000 US census data and to projected US population figures for 2020 to estimate the number of the US population with OAG. The overall prevalence of OAG in the US population 40 years and older is estimated to be 1.86% (95% confidence interval, 1.75%-1.96%), with 1.57 million white and 398 000 black persons affected. After applying race-, age-, and gender-specific rates to the US population as determined in the 2000 US census, we estimated that OAG affects 2.22 million US citizens. Owing to the rapidly aging population, the number with OAG will increase by 50% to 3.36 million in 2020. Black subjects had almost 3 times the age-adjusted prevalence of glaucoma than white subjects. Open-angle glaucoma affects more than 2 million individuals in the United States. Owing to the rapid aging of the US population, this number will increase to more than 3 million by 2020.
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              Retinal stem cells in the adult mammalian eye.

              The mature mammalian retina is thought to lack regenerative capacity. Here, we report the identification of a stem cell in the adult mouse eye, which represents a possible substrate for retinal regeneration. Single pigmented ciliary margin cells clonally proliferate in vitro to form sphere colonies of cells that can differentiate into retinal-specific cell types, including rod photoreceptors, bipolar neurons, and Müller glia. Adult retinal stem cells are localized to the pigmented ciliary margin and not to the central and peripheral retinal pigmented epithelium, indicating that these cells may be homologous to those found in the eye germinal zone of other nonmammalian vertebrates.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2012
                18 September 2012
                : 7
                : 9
                : e44973
                Affiliations
                [1 ]Department of Clinical and Molecular Ophthalmogenetics, the Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands
                [2 ]Laboratory for Neuroregeneration, the Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands
                [3 ]Department of Bioinformatics, Erasmus University Medical Center, Rotterdam, The Netherlands
                [4 ]Department of Ophthalmology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
                [5 ]Department of Ophthalmology, Academic Medical Centre, Amsterdam, The Netherlands
                [6 ]Department of Clinical Genetics, Academic Medical Centre, Amsterdam, The Netherlands
                University of Rochester, United States of America
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: SFJ JBtB AABB. Performed the experiments: SFJ JBtB AHWE MN. Analyzed the data: SFJ AABB KB PJvdS NMJ TGMFG. Contributed reagents/materials/analysis tools: PJvdS KB. Wrote the paper: SFJ AABB. Supervised: AABB.

                Article
                PONE-D-12-14050
                10.1371/journal.pone.0044973
                3445623
                23028713
                ffb9497c-2009-46a7-b309-3cebb8ff8d6f
                Copyright @ 2012

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 15 May 2012
                : 15 August 2012
                Page count
                Pages: 23
                Funding
                This study was supported by grants from the General Dutch Foundation Preventing Blindness, the National Foundation for Blinds and Low Vision, the Foundation Blinden-Penning, the Foundation Glaucoomfonds, the Rotterdam Foundation of Blinds and the Professor Mulder Foundation (all together cooperated by UitZicht, project # UitZicht2008-7). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology
                Computational Biology
                Genomics
                Functional Genomics
                Genome Expression Analysis
                Molecular Genetics
                Gene Expression
                Microarrays
                Genetics
                Gene Expression
                Molecular Genetics
                Genomics
                Functional Genomics
                Molecular Cell Biology
                Nucleic Acids
                RNA
                Gene Expression
                Medicine
                Ophthalmology
                Glaucoma

                Uncategorized
                Uncategorized

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