Human primary endothelial cells are impaired in nucleotide excision repair and sensitive to benzo[a]pyrene compared with smooth muscle cells and pericytes

Joana M. Kress, Lorella Di Dio, Larissa Heck, Alessandra Pulliero, Alberto Izzotti, Kathrin Laarmann, Gerhard Fritz, Bernd Kaina

Research output: Contribution to journalArticle

Abstract

The endothelium represents the inner cell layer of blood vessels and is supported by smooth muscle cells and pericytes, which form the vessel structure. The endothelium is involved in the pathogenesis of many diseases, including the development of atherosclerosis. Due to direct blood contact, the blood vessel endothelium is inevitably exposed to genotoxic substances that are systemically taken up by the body, including benzo[a]pyrene, which is a major genotoxic component in cigarette smoke and a common environmental mutagen and human carcinogen. Here, we evaluated the impact of benzo[a]pyrene diol epoxide (BPDE), which is the reactive metabolite of benzo[a]pyrene, on the three innermost vessel cell types. Primary human endothelial cells (HUVEC), primary human smooth muscle cells (HUASMC) and primary human pericytes (HPC) were treated with BPDE, and analyses of cytotoxicity, cellular senescence and genotoxic effects were then performed. The results showed that HUVEC were more sensitive to the cytotoxic activity of BPDE than HUASMC and HPC. We further show that HUVEC display a detraction in the repair of BPDE-induced adducts, as determined through the comet assay and the quantification of BPDE adducts in post-labelling experiments. A screening for DNA repair factors revealed that the nucleotide excision repair (NER) proteins ERCC1, XPF and ligase I were expressed at lower levels in HUVEC compared with HUASMC and HPC, which corresponds with the impaired NER-mediated removal of BPDE adducts from DNA. Taken together, the data revealed that HUVEC exhibit an unexpected DNA repair-impaired phenotype, which has implications on the response of the endothelium to genotoxicants that induce bulky DNA lesions, including the development of vascular diseases resulting from smoking and environmental pollution.

Original languageEnglish
Number of pages1
JournalScientific Reports
Volume9
Issue number1
DOIs
Publication statusPublished - Sep 24 2019

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Pericytes
Benzo(a)pyrene
DNA Repair
Smooth Muscle Myocytes
Epoxy Compounds
Endothelial Cells
Endothelium
Blood Vessels
Environmental Pollution
Comet Assay
DNA Adducts
Cell Aging
Mutagens
Ligases
Vascular Diseases
Smoke
Tobacco Products
Carcinogens
Atherosclerosis
Smoking

ASJC Scopus subject areas

  • General

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Human primary endothelial cells are impaired in nucleotide excision repair and sensitive to benzo[a]pyrene compared with smooth muscle cells and pericytes. / Kress, Joana M.; Dio, Lorella Di; Heck, Larissa; Pulliero, Alessandra; Izzotti, Alberto; Laarmann, Kathrin; Fritz, Gerhard; Kaina, Bernd.

In: Scientific Reports, Vol. 9, No. 1, 24.09.2019.

Research output: Contribution to journalArticle

Kress, Joana M. ; Dio, Lorella Di ; Heck, Larissa ; Pulliero, Alessandra ; Izzotti, Alberto ; Laarmann, Kathrin ; Fritz, Gerhard ; Kaina, Bernd. / Human primary endothelial cells are impaired in nucleotide excision repair and sensitive to benzo[a]pyrene compared with smooth muscle cells and pericytes. In: Scientific Reports. 2019 ; Vol. 9, No. 1.
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