Literature DB >> 9467963

Constitutive telomerase activity in cells with tissue-renewing potential from estrogen-regulated rat tissues.

A K Bednarek1, Y Chu, C M Aldaz.   

Abstract

To investigate the role of telomerase in estrogen-regulated rodent tissues, we assayed the activity levels of this enzyme and measured cell proliferation and indicators of cellularity in vagina, mammary gland, and uterus from virgin, pregnant, ovariectomized, and ovariectomized estradiol-treated rats. No association was observed between telomerase activity and increased cell proliferation. Telomerase activity was significantly higher (P=0.003) in vagina obtained from ovariectomized rats (very low proliferation) than in vagina from ovariectomized and estradiol-treated rats (high proliferation, high differentiation). The high telomerase levels observed in vagina from ovariectomized rats indicates that the same epithelial compartment (i.e., basal layer) that has the potential to reconstitute the epithelium also contains the cells that express telomerase. The lower telomerase activity in the keratinized (differentiated) vagina was probably due to dilution of the number of telomerase-producing cells by the terminally differentiated non-telomerase-producing cells. Similar results were observed in uterus from ovariectomized versus ovariectomized and estradiol-treated rats. Telomerase activity was highest in uterus from pregnant rats. Telomerase levels in samples from total mammary gland fat pads varied considerably between groups and appeared to be representative of the amount of epithelium present in the sample. Interestingly, when mammary gland samples from the same animals were obtained from pure epithelial organoid preparations, no differences in telomerase activity could be distinguished between animals or groups. Overall these data suggest that telomerase activity, particularly in rat vagina and uterus, appears to be associated with a cell subpopulation showing proliferative and tissue reconstitution potential and not directly associated with proliferation status per se.

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Year:  1998        PMID: 9467963     DOI: 10.1038/sj.onc.1201553

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  4 in total

1.  Induction of hTERT expression and telomerase activity by estrogens in human ovary epithelium cells.

Authors:  S Misiti; S Nanni; G Fontemaggi; Y S Cong; J Wen; H W Hirte; G Piaggio; A Sacchi; A Pontecorvi; S Bacchetti; A Farsetti
Journal:  Mol Cell Biol       Date:  2000-06       Impact factor: 4.272

2.  Retinoids down-regulate telomerase and telomere length in a pathway distinct from leukemia cell differentiation.

Authors:  F Pendino; M Flexor; F Delhommeau; D Buet; M Lanotte; E Segal-Bendirdjian
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-22       Impact factor: 11.205

3.  Prevention of critical telomere shortening by oestradiol in human normal hepatic cultured cells and carbon tetrachloride induced rat liver fibrosis.

Authors:  R Sato; C Maesawa; K Fujisawa; K Wada; K Oikawa; Y Takikawa; K Suzuki; H Oikawa; K Ishikawa; T Masuda
Journal:  Gut       Date:  2004-07       Impact factor: 23.059

Review 4.  Hormonal regulation of telomerase activity and hTERT expression in steroid-regulated tissues and cancer.

Authors:  Mohammad Taheri; Soudeh Ghafouri-Fard; Sajad Najafi; Julia Kallenbach; Elmira Keramatfar; Golnaz Atri Roozbahani; Mehdi Heidari Horestani; Bashdar Mahmud Hussen; Aria Baniahmad
Journal:  Cancer Cell Int       Date:  2022-08-16       Impact factor: 6.429

  4 in total

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