Oxidative stress-induced single-strand breaks in chromosomal telomeres of human retinal pigment epithelial cells in vitro

S. Honda, L. M. Hjelmeland, James Handa

Research output: Contribution to journalArticle

Abstract

PURPOSE. To demonstrate that chronic hyperoxia induces single-stranded breaks in chromosomal telomeres as a measure of oxidative DNA damage in cultured RPE cells. METHODS. RPE340 cells were cultured in 40% and 20% (control) O2. DNA damage was assessed by mean terminal restriction fragment (TRF) length, and the S1 nuclease assay was used to determine the frequency of single-strand breaks in telomeric DNA, The degree of oxidative stress in cells was estimated by flow cytometric analysis of reactive oxygen intermediate (ROI)-induced 2′,7′-dichlorodihydrofluorescein diacetate fluorescence and Northern blot analysis of heme oxygenase-1 (HO-1) mRNA induction. RESULTS. The mean TRF length of cells grown in 40% O2 shortened at a faster rate than those grown in 20% O2. The S1 nuclease assay showed that the accelerated mean TRF length shortening was due to an increased accumulation of single-stranded breaks in telomeric DNA. The degree of ROI production and HO-1 mRNA induction was greater in cells treated with 40% than 20% O2, an effect that was also larger in old than young passaged cells. CONCLUSIONS. RPE340 cells in vitro grown in chronic hyperoxia exhibited evidence of DNA damage with accelerated telomeric shortening via an increased accumulation of single-strand breaks in telomeric DNA. These changes could provide insight into aging of RPE cells by oxidative DNA damage.

Original languageEnglish (US)
Pages (from-to)2139-2144
Number of pages6
JournalInvestigative Ophthalmology and Visual Science
Volume42
Issue number9
StatePublished - 2001

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Chromosome Breakage
Retinal Pigments
Telomere
Oxidative Stress
Epithelial Cells
DNA Damage
Hyperoxia
Heme Oxygenase-1
Cultured Cells
DNA
Oxygen
Messenger RNA
Cell Aging
Northern Blotting
Fluorescence
In Vitro Techniques

ASJC Scopus subject areas

  • Ophthalmology

Cite this

Oxidative stress-induced single-strand breaks in chromosomal telomeres of human retinal pigment epithelial cells in vitro. / Honda, S.; Hjelmeland, L. M.; Handa, James.

In: Investigative Ophthalmology and Visual Science, Vol. 42, No. 9, 2001, p. 2139-2144.

Research output: Contribution to journalArticle

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abstract = "PURPOSE. To demonstrate that chronic hyperoxia induces single-stranded breaks in chromosomal telomeres as a measure of oxidative DNA damage in cultured RPE cells. METHODS. RPE340 cells were cultured in 40{\%} and 20{\%} (control) O2. DNA damage was assessed by mean terminal restriction fragment (TRF) length, and the S1 nuclease assay was used to determine the frequency of single-strand breaks in telomeric DNA, The degree of oxidative stress in cells was estimated by flow cytometric analysis of reactive oxygen intermediate (ROI)-induced 2′,7′-dichlorodihydrofluorescein diacetate fluorescence and Northern blot analysis of heme oxygenase-1 (HO-1) mRNA induction. RESULTS. The mean TRF length of cells grown in 40{\%} O2 shortened at a faster rate than those grown in 20{\%} O2. The S1 nuclease assay showed that the accelerated mean TRF length shortening was due to an increased accumulation of single-stranded breaks in telomeric DNA. The degree of ROI production and HO-1 mRNA induction was greater in cells treated with 40{\%} than 20{\%} O2, an effect that was also larger in old than young passaged cells. CONCLUSIONS. RPE340 cells in vitro grown in chronic hyperoxia exhibited evidence of DNA damage with accelerated telomeric shortening via an increased accumulation of single-strand breaks in telomeric DNA. These changes could provide insight into aging of RPE cells by oxidative DNA damage.",
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AU - Honda, S.

AU - Hjelmeland, L. M.

AU - Handa, James

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N2 - PURPOSE. To demonstrate that chronic hyperoxia induces single-stranded breaks in chromosomal telomeres as a measure of oxidative DNA damage in cultured RPE cells. METHODS. RPE340 cells were cultured in 40% and 20% (control) O2. DNA damage was assessed by mean terminal restriction fragment (TRF) length, and the S1 nuclease assay was used to determine the frequency of single-strand breaks in telomeric DNA, The degree of oxidative stress in cells was estimated by flow cytometric analysis of reactive oxygen intermediate (ROI)-induced 2′,7′-dichlorodihydrofluorescein diacetate fluorescence and Northern blot analysis of heme oxygenase-1 (HO-1) mRNA induction. RESULTS. The mean TRF length of cells grown in 40% O2 shortened at a faster rate than those grown in 20% O2. The S1 nuclease assay showed that the accelerated mean TRF length shortening was due to an increased accumulation of single-stranded breaks in telomeric DNA. The degree of ROI production and HO-1 mRNA induction was greater in cells treated with 40% than 20% O2, an effect that was also larger in old than young passaged cells. CONCLUSIONS. RPE340 cells in vitro grown in chronic hyperoxia exhibited evidence of DNA damage with accelerated telomeric shortening via an increased accumulation of single-strand breaks in telomeric DNA. These changes could provide insight into aging of RPE cells by oxidative DNA damage.

AB - PURPOSE. To demonstrate that chronic hyperoxia induces single-stranded breaks in chromosomal telomeres as a measure of oxidative DNA damage in cultured RPE cells. METHODS. RPE340 cells were cultured in 40% and 20% (control) O2. DNA damage was assessed by mean terminal restriction fragment (TRF) length, and the S1 nuclease assay was used to determine the frequency of single-strand breaks in telomeric DNA, The degree of oxidative stress in cells was estimated by flow cytometric analysis of reactive oxygen intermediate (ROI)-induced 2′,7′-dichlorodihydrofluorescein diacetate fluorescence and Northern blot analysis of heme oxygenase-1 (HO-1) mRNA induction. RESULTS. The mean TRF length of cells grown in 40% O2 shortened at a faster rate than those grown in 20% O2. The S1 nuclease assay showed that the accelerated mean TRF length shortening was due to an increased accumulation of single-stranded breaks in telomeric DNA. The degree of ROI production and HO-1 mRNA induction was greater in cells treated with 40% than 20% O2, an effect that was also larger in old than young passaged cells. CONCLUSIONS. RPE340 cells in vitro grown in chronic hyperoxia exhibited evidence of DNA damage with accelerated telomeric shortening via an increased accumulation of single-strand breaks in telomeric DNA. These changes could provide insight into aging of RPE cells by oxidative DNA damage.

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