Alternariol induces abnormal nuclear morphology and cell cycle arrest in murine RAW 264.7 macrophages

► AOH induces cell cycle arrest in the G2/M transition. ► The arrest is mediated by reduced activity of the cyclin B1/cdc-2 complex. ► AOH induces abnormally shaped nuclei, likely as a result of incomplete decatenation. The mycotoxin alternariol (AOH), a frequent contaminant in fruit and cereal prod...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Toxicology letters 2013-05, Vol.219 (1), p.8-17
Hauptverfasser: Solhaug, A., Holme, J.A., Haglund, K., Dendele, B., Sergent, O., Pestka, J., Lagadic-Gossmann, D., Eriksen, G.S.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:► AOH induces cell cycle arrest in the G2/M transition. ► The arrest is mediated by reduced activity of the cyclin B1/cdc-2 complex. ► AOH induces abnormally shaped nuclei, likely as a result of incomplete decatenation. The mycotoxin alternariol (AOH), a frequent contaminant in fruit and cereal products, is known to induce DNA damage with subsequent cell cycle arrest. Here we elucidated the effects of AOH on stages of cell cycle progression using the RAW 264.7 macrophage model. AOH resulted in an accumulation of cells in the G2/M-phase (4N). Most cells exhibited a large G2 nucleus whereas numbers of true mitotic cells were reduced relative to control. Both cyclin B1 and p-cdc2 levels increased, while cyclin B1 remained in the cytoplasm; suggesting arrest in the G2/M transition point. Remarkably, after exposure to AOH for 24h, most of the cells exhibited abnormally shaped nuclei, as evidenced by partly divided nuclei, nuclear blebs, polyploidy and micronuclei (MN). AOH treatment also induced abnormal Aurora B bridges, suggesting that cytokinesis was interfered within cells undergoing karyokinesis. A minor part of the resultant G1 tetraploid (4N) cells re-entered the S-phase and progressed to 8N cells.
ISSN:0378-4274
1879-3169
DOI:10.1016/j.toxlet.2013.02.012