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2014 | 61 | 2 | 265-270
Article title

The influence of elastin degradation products, glucose and atorvastatin on metalloproteinase-1, -2, -9 and tissue inhibitor of metalloproteinases-1, -2, -3 expression in human retinal pigment epithelial cells

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Abstracts
EN
Purpose: Hyperglycemia and increased concentrations of elastin degradation products (EDPs) are common findings in patients with diabetes, atherosclerosis and hypertension. The aim of this study was to assess the influence of high glucose, EDPs and atorvastatin on MMP-1, MMP-2, MMP-9 and TIMP1-3 gene expression in human retinal pigment epithelial cells (HRPE) in vitro. Method: HRPE were cultured for 24 hours with the substances being tested (glucose, EDPs), alone or in combination. Additionally, the cells were treated with atorvastatin in two different concentrations (1 or 10 μM). After incubation, total cellular RNA was extracted and used for gene expression evaluation. Gene expression was measured using the real-time RT-PCR technique. Results: Glucose, EDPs and atorvastatin had no impact on TIMP-1 and TIMP-3 expression. HRPE cells treated with glucose or EDPs with the addition of atorvastatin had a statistically significant decrease of TIMP-2 expression; glucose alone decreased MMP-1 expression. Atorvastatin decreased expression of all assessed genes, except TIMP-1 and TIMP-3 in a dose-dependent manner. Conclusions: Our results confirm the importance of MMPs and TIMPs in retinal vascular biology. Atorvastatin-induced MMPs gene expression can deeply affect extracellular matrix turnover, which may play an important role in the progression of ocular diseases.
Keywords
Year
Volume
61
Issue
2
Pages
265-270
Physical description
Dates
published
2014
received
2013-06-14
revised
2014-03-26
accepted
2014-04-04
(unknown)
2014-06-06
Contributors
  • Department of Ophthalmology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland
  • Department of Biochemistry, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland
  • Department of Biochemistry, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland
  • Department of Biochemistry, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland
  • Department of Ophthalmology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland
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Document Type
Publication order reference
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YADDA identifier
bwmeta1.element.bwnjournal-article-abpv61p265kz
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