Enhanced Eryptosis Following Juglone Exposure. (21st November 2014)
- Record Type:
- Journal Article
- Title:
- Enhanced Eryptosis Following Juglone Exposure. (21st November 2014)
- Main Title:
- Enhanced Eryptosis Following Juglone Exposure
- Authors:
- Calabrò, Salvatrice
Alzoubi, Kousi
Bissinger, Rosi
Jilani, Kashif
Faggio, Caterina
Lang, Florian - Abstract:
- <abstract abstract-type="main" id="bcpt12340-abs-0001"> <title>Abstract</title> <p>Juglone, a quinone isolated from <italic>Juglans mandshurica Maxim</italic>, has previously been shown to be effective against malignancy. The effect is at least partially due to stimulation of suicidal death or apoptosis of tumour cells. On the other hand, juglone has been shown to counteract apoptosis, for example, of neurons. In analogy to apoptosis of nucleated cells, erythrocytes may enter eryptosis, a suicidal death characterized by cell shrinkage and breakdown of phosphatidylserine asymmetry of the cell membrane with phosphatidylserine exposure at the erythrocyte surface. Stimulators of eryptosis include increase in cytosolic Ca<sup>2+</sup> activity [(Ca<sup>2+</sup>)<sub>i</sub>]. This study explored whether juglone stimulates eryptosis. To this end, erythrocyte volume was estimated from forward scatter, phosphatidylserine exposure at the erythrocyte surface from FITC annexin V binding, ceramide abundance from binding of fluorescent antibodies in flow cytometry and cytosolic ATP with a luciferin–luciferase‐based assay. As a result, a 24‐hr exposure of human erythrocytes to juglone (5 μM) significantly decreased erythrocyte forward scatter. Juglone (1–5 μM) significantly increased the percentage of annexin V binding cells. Juglone (5 μM) significantly increased ceramide abundance at the erythrocyte surface and decreased erythrocyte ATP concentration. The effect of juglone (10 μM) on<abstract abstract-type="main" id="bcpt12340-abs-0001"> <title>Abstract</title> <p>Juglone, a quinone isolated from <italic>Juglans mandshurica Maxim</italic>, has previously been shown to be effective against malignancy. The effect is at least partially due to stimulation of suicidal death or apoptosis of tumour cells. On the other hand, juglone has been shown to counteract apoptosis, for example, of neurons. In analogy to apoptosis of nucleated cells, erythrocytes may enter eryptosis, a suicidal death characterized by cell shrinkage and breakdown of phosphatidylserine asymmetry of the cell membrane with phosphatidylserine exposure at the erythrocyte surface. Stimulators of eryptosis include increase in cytosolic Ca<sup>2+</sup> activity [(Ca<sup>2+</sup>)<sub>i</sub>]. This study explored whether juglone stimulates eryptosis. To this end, erythrocyte volume was estimated from forward scatter, phosphatidylserine exposure at the erythrocyte surface from FITC annexin V binding, ceramide abundance from binding of fluorescent antibodies in flow cytometry and cytosolic ATP with a luciferin–luciferase‐based assay. As a result, a 24‐hr exposure of human erythrocytes to juglone (5 μM) significantly decreased erythrocyte forward scatter. Juglone (1–5 μM) significantly increased the percentage of annexin V binding cells. Juglone (5 μM) significantly increased ceramide abundance at the erythrocyte surface and decreased erythrocyte ATP concentration. The effect of juglone (10 μM) on annexin V binding was slightly but significantly blunted by removal of extracellular Ca<sup>2+</sup> and by addition of protein kinase C (PKC) inhibitor staurosporine (1 μM). In conclusion, juglone stimulates suicidal erythrocyte death or eryptosis at least in part by upregulation of ceramide abundance, energy depletion and activation of PKC.</p> </abstract> … (more)
- Is Part Of:
- Basic & clinical pharmacology & toxicology. Volume 116:Number 6(2015:Jun.)
- Journal:
- Basic & clinical pharmacology & toxicology
- Issue:
- Volume 116:Number 6(2015:Jun.)
- Issue Display:
- Volume 116, Issue 6 (2015)
- Year:
- 2015
- Volume:
- 116
- Issue:
- 6
- Issue Sort Value:
- 2015-0116-0006-0000
- Page Start:
- 460
- Page End:
- 467
- Publication Date:
- 2014-11-21
- Subjects:
- Pharmacology -- Periodicals
Toxicology -- Periodicals
Pharmacology -- Periodicals
Toxicology -- Periodicals
Pharmacology, Clinical -- Periodicals
Computer network resources
Electronic journals
615.1 - Journal URLs:
- http://firstsearch.oclc.org/journal=1742-7835;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1742-7843 ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=pto ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bcpt.12340 ↗
- Languages:
- English
- ISSNs:
- 1742-7835
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1863.914250
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3413.xml