Statins decrease vascular epithelial growth factor expression via down-regulation of receptor for advanced glycation end-products. Issue 9 (September 2017)
- Record Type:
- Journal Article
- Title:
- Statins decrease vascular epithelial growth factor expression via down-regulation of receptor for advanced glycation end-products. Issue 9 (September 2017)
- Main Title:
- Statins decrease vascular epithelial growth factor expression via down-regulation of receptor for advanced glycation end-products
- Authors:
- Tsujinaka, Hiroki
Itaya-Hironaka, Asako
Yamauchi, Akiyo
Sakuramoto-Tsuchida, Sumiyo
Shobatake, Ryogo
Makino, Mai
Masuda, Naonori
Hirai, Hiromasa
Takasawa, Shin
Ogata, Nahoko - Abstract:
- ABSTRACT: Aims: Statins, inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A reductase, possess pleiotropic effects that have been extended to modulation of various cellular behaviors. This study aimed to examine whether statins modulate vascular endothelial growth factor A ( VEGF-A ) expression in human retinal pigment epithelium (RPE) cells. Main methods: Human RPE cells (h1RPE7), damaged by hydroquinone (HQ) + advanced glycation endproducts (AGE) in an in vitro AMD model, were treated with atorvastatin or lovastatin for 24 h. The expression of VEGF-A and receptor for AGE ( RAGE ) was evaluated by real-time RT-PCR. VEGF-A secretion was measured by ELISA. To investigate the impact of RAGE on VEGF-A expression, small interfering RNA (siRNA) for RAGE ( siRAGE ) was introduced into h1RPE7 cells and VEGF-A expression was measured by real-time RT-PCR. Deletions of VEGF-A and RAGE promoters were performed and transcriptional activities were measured after the addition of statins to HQ + AGE-damaged RPE cells. Key findings: The mRNA levels of VEGF-A and RAGE and the levels of VEGF-A in the culture medium were increased by HQ + AGE. Both atorvastatin and lovastatin attenuated HQ + AGE-induced VEGF-A and RAGE expression. These statins also decreased VEGF-A levels in the culture medium. RNA interference of RAGE attenuated the up-regulation of VEGF-A in the HQ + AGE treated cells. The deletion analysis demonstrated that these statins attenuated RAGE promoter activation in HQ +ABSTRACT: Aims: Statins, inhibitors of 3-hydroxy-3-methylglutaryl coenzyme A reductase, possess pleiotropic effects that have been extended to modulation of various cellular behaviors. This study aimed to examine whether statins modulate vascular endothelial growth factor A ( VEGF-A ) expression in human retinal pigment epithelium (RPE) cells. Main methods: Human RPE cells (h1RPE7), damaged by hydroquinone (HQ) + advanced glycation endproducts (AGE) in an in vitro AMD model, were treated with atorvastatin or lovastatin for 24 h. The expression of VEGF-A and receptor for AGE ( RAGE ) was evaluated by real-time RT-PCR. VEGF-A secretion was measured by ELISA. To investigate the impact of RAGE on VEGF-A expression, small interfering RNA (siRNA) for RAGE ( siRAGE ) was introduced into h1RPE7 cells and VEGF-A expression was measured by real-time RT-PCR. Deletions of VEGF-A and RAGE promoters were performed and transcriptional activities were measured after the addition of statins to HQ + AGE-damaged RPE cells. Key findings: The mRNA levels of VEGF-A and RAGE and the levels of VEGF-A in the culture medium were increased by HQ + AGE. Both atorvastatin and lovastatin attenuated HQ + AGE-induced VEGF-A and RAGE expression. These statins also decreased VEGF-A levels in the culture medium. RNA interference of RAGE attenuated the up-regulation of VEGF-A in the HQ + AGE treated cells. The deletion analysis demonstrated that these statins attenuated RAGE promoter activation in HQ + AGE-damaged RPE cells. Significance: Statins attenuated HQ + AGE-induced VEGF expression by decreasing RAGE expression. As VEGF is an important factor in developing wet AMD, statins could decrease the risk of wet-type AMD and be used as preventive medicines. … (more)
- Is Part Of:
- Heliyon. Volume 3:Issue 9(2017)
- Journal:
- Heliyon
- Issue:
- Volume 3:Issue 9(2017)
- Issue Display:
- Volume 3, Issue 9 (2017)
- Year:
- 2017
- Volume:
- 3
- Issue:
- 9
- Issue Sort Value:
- 2017-0003-0009-0000
- Page Start:
- Page End:
- Publication Date:
- 2017-09
- Subjects:
- Biological sciences -- Ophthalmology -- Biochemistry -- Cell biology
Research -- Periodicals
Medical sciences -- Periodicals
Natural history -- Periodicals
Social sciences -- Periodicals
Earth sciences -- Periodicals
Physical sciences -- Periodicals
507.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/24058440/ ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.heliyon.2017.e00401 ↗
- Languages:
- English
- ISSNs:
- 2405-8440
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4708.xml