Porcine brain microvessel endothelial cells show pro-inflammatory response to the size and composition of metallic nanoparticles. (May 2014)
- Record Type:
- Journal Article
- Title:
- Porcine brain microvessel endothelial cells show pro-inflammatory response to the size and composition of metallic nanoparticles. (May 2014)
- Main Title:
- Porcine brain microvessel endothelial cells show pro-inflammatory response to the size and composition of metallic nanoparticles
- Authors:
- Trickler, William J.
Lantz-McPeak, Susan M.
Robinson, Bonnie L.
Paule, Merle G.
Slikker, William
Biris, Alexandru S.
Schlager, John J.
Hussain, Saber M.
Kanungo, Jyotshna
Gonzalez, Carmen
Ali, Syed F. - Abstract:
- <abstract> <title>Abstract</title> <p>The purpose of the current studies was to determine if systemic exposure of various metallic nanoparticles differing in size and composition [silver (Ag-NPs, 25, 40 and 80 nm), copper-oxide (Cu-NPs, 40 and 60 nm) or gold (Au-NPs, 3 and 5 nm)] can induce the release of pro-inflammatory mediators that influence the restrictive nature of the blood–brain barrier (BBB) <italic>in vitro.</italic> Confluent porcine brain microvessel endothelial cells (pBMECs) (8–12 days) were treated with various metallic nanoparticles (15 μg/ml). Extracellular concentrations of pro-inflammatory mediators (IL-1β, TNFα and PGE<sub>2</sub>) were evaluated using ELISA. pBMECs were cultured in standard 12-well Transwell® inserts, and permeability was evaluated by measuring the transport of fluorescein across the pBMEC monolayers. PGE<sub>2</sub> release following Cu-NP exposure was significantly increased when compared to the control. Similar results were observed for Ag-NPs but not Au-NPs. The secretion of TNFα and IL-1β was observed for both Cu-NPs and Ag-NPs but not in response to Au-NPs. The post-treatment time profiles of TNFα and IL-1β revealed that the IL-1β response was more persistent. The permeability ratios (exposure/control) were significantly greater following exposure to Cu-NPs or Ag-NPs, compared to Au-NPs. Together, these data suggest that the composition and size of NPs can cause significant pro-inflammatory response that can influence the<abstract> <title>Abstract</title> <p>The purpose of the current studies was to determine if systemic exposure of various metallic nanoparticles differing in size and composition [silver (Ag-NPs, 25, 40 and 80 nm), copper-oxide (Cu-NPs, 40 and 60 nm) or gold (Au-NPs, 3 and 5 nm)] can induce the release of pro-inflammatory mediators that influence the restrictive nature of the blood–brain barrier (BBB) <italic>in vitro.</italic> Confluent porcine brain microvessel endothelial cells (pBMECs) (8–12 days) were treated with various metallic nanoparticles (15 μg/ml). Extracellular concentrations of pro-inflammatory mediators (IL-1β, TNFα and PGE<sub>2</sub>) were evaluated using ELISA. pBMECs were cultured in standard 12-well Transwell® inserts, and permeability was evaluated by measuring the transport of fluorescein across the pBMEC monolayers. PGE<sub>2</sub> release following Cu-NP exposure was significantly increased when compared to the control. Similar results were observed for Ag-NPs but not Au-NPs. The secretion of TNFα and IL-1β was observed for both Cu-NPs and Ag-NPs but not in response to Au-NPs. The post-treatment time profiles of TNFα and IL-1β revealed that the IL-1β response was more persistent. The permeability ratios (exposure/control) were significantly greater following exposure to Cu-NPs or Ag-NPs, compared to Au-NPs. Together, these data suggest that the composition and size of NPs can cause significant pro-inflammatory response that can influence the integrity of the BBB.</p> </abstract> … (more)
- Is Part Of:
- Drug metabolism reviews. Volume 46:Number 2(2014:Apr.)
- Journal:
- Drug metabolism reviews
- Issue:
- Volume 46:Number 2(2014:Apr.)
- Issue Display:
- Volume 46, Issue 2 (2014)
- Year:
- 2014
- Volume:
- 46
- Issue:
- 2
- Issue Sort Value:
- 2014-0046-0002-0000
- Page Start:
- 224
- Page End:
- 231
- Publication Date:
- 2014-05
- Subjects:
- Drugs -- Metabolism -- Periodicals
Pharmacokinetics -- Periodicals
Pharmaceutical Preparations -- metabolism -- Periodicals
615 - Journal URLs:
- http://informahealthcare.com/loi/dmr ↗
http://informahealthcare.com ↗ - DOI:
- 10.3109/03602532.2013.873450 ↗
- Languages:
- English
- ISSNs:
- 0360-2532
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3629.330000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3423.xml