Literature DB >> 532757

[Mitotic activity of the pigment epithelium during embryonic and postembryonic development].

S Kaldarar-Pedotti.   

Abstract

The purpose of the present study was to examine the mitotic activity of the normal pigment epithelium of the retina (RPE), the ciliary body and the iris of different animals during gestation and after birth by blocking the metaphase with colchicine and by marking the pigment epithelial nuclei with tritium-labeled thymidine. The colchicine examinations were made on 54 albino rabbits and 56 albino rats, the 3H-thymidine studies with 78 albino mice. In the rabbit the peak of mitotic activity (respectively the end) is found in the RPE at the beginning of the 2nd third of gestation (respectively at the 9th postnatal day), but in the pigment epithelium of the ciliary body and in the iris during the last third of gestation (respectively in the 2nd month of life and the 3rd postnatal week). In the rat the highest mitotic activity is reached in the RPE at the beginning of the 2nd half of gestation (respectively at the 13th postnatal day), in the ciliary body at the 3rd day of life (respectively the 24th postnatal day) and in the iris at the end of the gestational period (respectively the 17th postnatal day). In the mouse the highest rates of mitotic activity are found in the RPE from the 16th gestational day to the 8th day of life (respectively the 20th day of life), in the ciliary body from the 1st to the 4th day of life (respectively from the 12th to the 20th postnatal day) and in the iris on the 9th day of life (respectively the 12th to the 20th postnatal day). The present observations have also demonstrated that with maturation of all areas of the pigment epithelium, the mitotic activity stops. The cells of the pigment epithelium do not have an epithelial cell turnover but they are reversible postmitotic cells. Despite the enormous proliferative properties the pigment epithelium shows no regeneration by mitosis after severe damage.

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Year:  1979        PMID: 532757

Source DB:  PubMed          Journal:  Adv Ophthalmol        ISSN: 0065-3004


  6 in total

1.  [Methodological limitations in the use of human donor eyes exemplified by age-related alterations in cell density of the retinal pigment epithelium].

Authors:  M Böhm
Journal:  Ophthalmologe       Date:  2017-07       Impact factor: 1.059

2.  Gossypol Acetic Acid Prevents Oxidative Stress-Induced Retinal Pigment Epithelial Necrosis by Regulating the FoxO3/Sestrin2 Pathway.

Authors:  Jakub Hanus; Hongmei Zhang; David H Chen; Qinbo Zhou; Peng Jin; Qinghua Liu; Shusheng Wang
Journal:  Mol Cell Biol       Date:  2015-03-23       Impact factor: 4.272

3.  Quantitative autofluorescence and cell density maps of the human retinal pigment epithelium.

Authors:  Thomas Ach; Carrie Huisingh; Gerald McGwin; Jeffrey D Messinger; Tianjiao Zhang; Mark J Bentley; Danielle B Gutierrez; Zsolt Ablonczy; R Theodore Smith; Kenneth R Sloan; Christine A Curcio
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-07-17       Impact factor: 4.799

Review 4.  RPE necroptosis in response to oxidative stress and in AMD.

Authors:  Jakub Hanus; Chastain Anderson; Shusheng Wang
Journal:  Ageing Res Rev       Date:  2015-09-11       Impact factor: 10.895

5.  In situ regeneration of retinal pigment epithelium by gene transfer of E2F2: a potential strategy for treatment of macular degenerations.

Authors:  D Kampik; M Basche; U F O Luhmann; K M Nishiguchi; J A E Williams; J Greenwood; S E Moss; H Han; S Azam; Y Duran; S J Robbie; J W B Bainbridge; D F Larkin; A J Smith; R R Ali
Journal:  Gene Ther       Date:  2017-11-30       Impact factor: 5.250

6.  AIF-independent parthanatos in the pathogenesis of dry age-related macular degeneration.

Authors:  Ki-Hong Jang; Yun-Ju Do; Dongwon Son; Eunji Son; Jun-Sub Choi; Eunhee Kim
Journal:  Cell Death Dis       Date:  2017-01-05       Impact factor: 8.469

  6 in total

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