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Triggering of Programmed Erythrocyte Death by Alantolactone

Department of Physiology, University of Tübingen, Gmelinstr. 5, 72076 Tuebingen, Germany
Department of Biological and Environmental Sciences, University of Messina, Viale Ferdinando Stagno d'Alcontres 31, 98166 S. Agata-Messina, Italy
Author to whom correspondence should be addressed.
Toxins 2014, 6(12), 3596-3612;
Received: 13 October 2014 / Revised: 10 December 2014 / Accepted: 17 December 2014 / Published: 22 December 2014
The sesquiterpene alantolactone counteracts malignancy, an effect at least in part due to stimulation of suicidal death or apoptosis of tumor cells. Signaling of alantolactone induced apoptosis involves altered gene expression and mitochondrial depolarization. Erythrocytes lack mitochondria and nuclei but may enter suicidal death or eryptosis, which is characterized by cell shrinkage and cell membrane scrambling with phosphatidylserine exposure at the erythrocyte surface. Cellular mechanisms involved in triggering of eryptosis include increase of cytosolic Ca2+-activity ([Ca2+]i) and oxidative stress. The present study explored, whether alantolactone stimulates eryptosis. To this end, erythrocyte volume was estimated from forward scatter, phosphatidylserine-exposure at the erythrocyte surface from FITC-annexin-V-binding, [Ca2+]i from Fluo3-fluorescence, ceramide abundance from binding of fluorescent antibodies, and oxidative stress from 2',7'-dichlorodihydrofluorescein-diacetate (DCFDA) fluorescence. As a result, a 48 h exposure of human erythrocytes to alantolactone (≥20 μM) significantly decreased erythrocyte forward scatter and increased the percentage of annexin-V-binding cells. Alantolactone significantly increased Fluo3 fluorescence (60 μM), ceramide abundance (60 μM) and DCFDA fluorescence (≥40 μM). The effect of alantolactone (60 μM) on annexin-V-binding was not significantly modified by removal of extracellular Ca2+. In conclusion, alantolactone stimulates suicidal erythrocyte death or eryptosis, an effect paralleled by increase of [Ca2+]i, ceramide abundance and oxidative stress. View Full-Text
Keywords: phosphatidylserine; alantolactone; ceramide; oxidative stress; cell volume; eryptosis phosphatidylserine; alantolactone; ceramide; oxidative stress; cell volume; eryptosis
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MDPI and ACS Style

Alzoubi, K.; Calabrò, S.; Egler, J.; Faggio, C.; Lang, F. Triggering of Programmed Erythrocyte Death by Alantolactone. Toxins 2014, 6, 3596-3612.

AMA Style

Alzoubi K, Calabrò S, Egler J, Faggio C, Lang F. Triggering of Programmed Erythrocyte Death by Alantolactone. Toxins. 2014; 6(12):3596-3612.

Chicago/Turabian Style

Alzoubi, Kousi, Salvatrice Calabrò, Jasmin Egler, Caterina Faggio, and Florian Lang. 2014. "Triggering of Programmed Erythrocyte Death by Alantolactone" Toxins 6, no. 12: 3596-3612.

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