Literature DB >> 19833124

Held under arrest: Many mature albino RPE cells display polyploidal features consistent with abnormal cell cycle retention.

Tom Adams, Golnaz Shahabi, Jaimie Hoh-Kam, Glen Jeffery.   

Abstract

A population of peripheral retinal pigment epithelium (RPE) cells in mature pigmented rats are retained in the cell cycle and divide, as determined by Ki67 and BrdU labeling. Their cell cycle rate is approximately 5 days. Ten times as many Ki67 positive cells are found in albinos compared with pigmented animals, but it is not known if they actually divide or only express cell cycle markers. In spite of the increased number of cells expressing cell cycle markers, we show here using BrdU, that levels of cell division in albino RPE are similar to those in pigmented animals and have a similar cell cycle rate. Hence, cell cycle activity does not progress through to cell division in the majority of albino RPE cells. Peripheral RPE cells in albinos are different from those in pigmented animals. Many have very large distorted or highly fragmented nuclei. These data along with patterns of Ki67 and BrdU labeling are consistent with such cells being retained abnormally in the cell cycle, replicating their DNA, but not able to progress through to full cell division. Hence, there are two populations of RPE cells in albinos, those undergoing normal cell division and those that appear to be arrested in the cell cycle. These abnormalities are present from early postnatal stages. Copyright 2009 Elsevier Ltd. All rights reserved.

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Year:  2009        PMID: 19833124     DOI: 10.1016/j.exer.2009.10.002

Source DB:  PubMed          Journal:  Exp Eye Res        ISSN: 0014-4835            Impact factor:   3.467


  7 in total

1.  Microscopic mammalian retinal pigment epithelium lesions induce widespread proliferation with differences in magnitude between center and periphery.

Authors:  Peter Lundh von Leithner; Coziana Ciurtin; Glen Jeffery
Journal:  Mol Vis       Date:  2010-03-31       Impact factor: 2.367

2.  Retinal pigment epithelial integrity is compromised in the developing albino mouse retina.

Authors:  Lena Iwai-Takekoshi; Anna Ramos; Ari Schaler; Samuel Weinreb; Richard Blazeski; Carol Mason
Journal:  J Comp Neurol       Date:  2016-05-19       Impact factor: 3.215

3.  Mature peripheral RPE cells have an intrinsic capacity to proliferate; a potential regulatory mechanism for age-related cell loss.

Authors:  Ioannis Kokkinopoulos; Golnaz Shahabi; Alan Colman; Glen Jeffery
Journal:  PLoS One       Date:  2011-04-22       Impact factor: 3.240

4.  Increased Oxidative and Nitrative Stress Accelerates Aging of the Retinal Vasculature in the Diabetic Retina.

Authors:  Folami Lamoke; Sean Shaw; Jianghe Yuan; Sudha Ananth; Michael Duncan; Pamela Martin; Manuela Bartoli
Journal:  PLoS One       Date:  2015-10-14       Impact factor: 3.240

5.  Regulation of retinal pigment epithelial cell phenotype by Annexin A8.

Authors:  Katharina Lueck; Amanda-Jayne F Carr; Dimitrios Stampoulis; Volker Gerke; Ursula Rescher; John Greenwood; Stephen E Moss
Journal:  Sci Rep       Date:  2017-07-05       Impact factor: 4.379

6.  In vitro disease modeling of oculocutaneous albinism type 1 and 2 using human induced pluripotent stem cell-derived retinal pigment epithelium.

Authors:  Aman George; Ruchi Sharma; Tyler Pfister; Mones Abu-Asab; Nathan Hotaling; Devika Bose; Charles DeYoung; Justin Chang; David R Adams; Tiziana Cogliati; Kapil Bharti; Brian P Brooks
Journal:  Stem Cell Reports       Date:  2022-01-11       Impact factor: 7.765

7.  The Dct-/- Mouse Model to Unravel Retinogenesis Misregulation in Patients with Albinism.

Authors:  Angèle Tingaud-Sequeira; Elina Mercier; Vincent Michaud; Benoît Pinson; Ivet Gazova; Etienne Gontier; Fanny Decoeur; Lisa McKie; Ian J Jackson; Benoît Arveiler; Sophie Javerzat
Journal:  Genes (Basel)       Date:  2022-06-27       Impact factor: 4.141

  7 in total

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