Aqueous extract of bulbus Fritillaria cirrhosa induces cytokinesis failure by blocking furrow ingression in human colon epithelial NCM460 cells
[Display omitted] •BFC induces binucleation and multinucleation.•BFC causes cytokinesis failure via inhibiting furrow ingression.•BFC deregulates the expression of genes implicated in contractile ring assembly.•BFC treatment generates micronuclei, nuclear buds and enlarged nuclei.•BFC-induced binucl...
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Veröffentlicht in: | Mutation research 2020-02, Vol.850-851, p.503147, Article 503147 |
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•BFC induces binucleation and multinucleation.•BFC causes cytokinesis failure via inhibiting furrow ingression.•BFC deregulates the expression of genes implicated in contractile ring assembly.•BFC treatment generates micronuclei, nuclear buds and enlarged nuclei.•BFC-induced binucleated cells may act as intermediates to produce genetically heterogeneous progenies.
Bulbus Fritillariacirrhosa D. Don (BFC) has been widely used as an herbal medicament for respiratory diseases in China for over 2000 years. The ethnomedicinal effects of BFC have been scientifically verified, nevertheless its toxicity has not been completely studied. Previously, we have reported that the aqueous extract of BFC induces mitotic aberrations and chromosomal instability (CIN) in human colon epithelial NCM460 cells via dysfunctioning the mitotic checkpoint. Here, we extend this study and specifically focus on the influence of BFC on cytokinesis, the final step of cell division. One remarkable change in NCM460 cells following BFC treatment is the high incidence of binucleated cells (BNCs). More detailed investigation of the ana-telophases reveals that furrow ingression, the first stage of cytokinesis, is inhibited by BFC. Asynchronous cultures treatment demonstrates that furrow ingression defects induced by BFCs are highly associated with the formation of BNCs in ensuing interphase, indicating the BNCs phenotype after BFC treatment was resulted from cytokinesis failure. In line with this, the expression of genes involved in the regulation of furrow ingression is significantly de-regulated by BFC (e.g., LATS-1/2 and Aurora-B are upregulated, and YB-1 is downregulated). Furthermore, long-term treatment of BFC elucidates that the BNCs phenotype is transient and the loss of BNCs is associated with increased frequency of micronuclei and nuclear buds, two biomarkers of CIN. In supporting of these findings, the Nin Jiom Pei Pa Koa and Chuanbei Pipa Gao, two commercially available Chinese traditional medicines containing BFC, are able to induce multinucleation and CIN in NCM460 cells. Altogether, these data provide the first in vitro experimental evidence linking BFC to cytokinesis failure and suggest the resultant BNCs may be intermediates to produce CIN progenies. |
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ISSN: | 1383-5718 1879-3592 1873-135X |
DOI: | 10.1016/j.mrgentox.2020.503147 |